11573/1684185 - 2023 -
The relationship between motor symptoms, signs, and parkinsonism with facial emotion recognition deficits in individuals with 22q11.2 deletion syndrome at high genetic risk for psychosis Accinni, Tommaso; Fanella, Martina; Frascarelli, Marianna; Buzzanca, Antonino; Kotzalidis, Georgios D.; Putotto, Carolina; Marino, Bruno; Panzera, Alessia; Moschillo, Antonella; Pasquini, Massimo; Biondi, Massimo; Di Bonaventura, Carlo; Di Fabio, Fabio - 01a Articolo in rivista
rivista: ACTA NEUROLOGICA SCANDINAVICA (Oxford : Blackwell) pp. 1-10 - issn: 1600-0404 - wos: WOS:000967294600001 (0) - scopus: 2-s2.0-85176148293 (0)
11573/1684180 - 2023 -
Prenatal screening and diagnostic considerations for 22q11.2 microdeletions Blagowidow, Natalie; Nowakowska, Beata; Schindewolf, Erica; Romana Grati, Francesca; Putotto, Carolina; Breckpot, Jeroen; Swillen, Ann; Blaine Crowley, Terrence; Loo, Joanne C. Y.; Lairson, Lauren A.; Óskarsdóttir, Sólveig; Boot, Erik; Garcia-Minaur, Sixto; Cristina Digilio, Maria; Marino Taussig De Bodonia, Bruno; Coleman, Beverly; Moldenhauer, Julie S.; Bassett, Anne S.; Mcdonald-Mcginn, Donna M. - 01a Articolo in rivista
rivista: GENES (Basel : Molecular Diversity Preservation International) pp. 160- - issn: 2073-4425 - wos: WOS:000915190100001 (8) - scopus: 2-s2.0-85146758210 (11)
11573/1670885 - 2023 -
Recognition of facial emotion expressions and perceptual processes in 22q11.2 deletion syndrome Buzzanca, A.; Accinni, T.; Frascarelli, M.; Troisi, E.; Kotzalidis, G. D.; Di Bonaventura, C.; Fanella, M.; Putotto, C.; Marino, B.; Pasquini, M.; Biondi, M.; Di Fabio, F. - 01a Articolo in rivista
rivista: EARLY INTERVENTION IN PSYCHIATRY (Blackwell Publishing) pp. 76-84 - issn: 1751-7885 - wos: WOS:000778601800001 (2) - scopus: 2-s2.0-85127240522 (2)
11573/1702621 - 2023 -
Social cognition and real‐life functioning in patient samples with 22q11.2 deletion syndrome with or without psychosis, compared to a large sample of patients with schizophrenia only and healthy controls Frascarelli, Marianna; Accinni, Tommaso; Buzzanca, Antonino; Carlone, Luca; Ghezzi, Francesco; Moschillo, Antonella; Kotzalidis, Georgios D.; Bucci, Paola; Giordano, Giulia Maria; Fanella, Martina; Di Bonaventura, Carlo; Putotto, Carolina; Marino Taussig De Bodonia, Bruno; Pasquini, Massimo; Biondi, Massimo; Di Fabio, Fabio - 01a Articolo in rivista
rivista: JOURNAL OF NEUROPSYCHOLOGY ([Leicester] : British Psychological Society) pp. 564-583 - issn: 1748-6653 - wos: WOS:000985648300001 (0) - scopus: 2-s2.0-85158990260 (0)
11573/1684078 - 2023 -
Updated clinical practice recommendations for managing children with 22q11.2 deletion syndrome Óskarsdóttir, Sólveig; Boot, Erik; Crowley, Terrence Blaine; Loo, Joanne C Y; Arganbright, Jill M; Armando, Marco; Baylis, Adriane L; Breetvelt, Elemi J; Castelein, René M; Chadehumbe, Madeline; Cielo, Christopher M; De Reuver, Steven; Eliez, Stephan; Fiksinski, Ania M; Forbes, Brian J; Gallagher, Emily; Hopkins, Sarah E; Jackson, Oksana A; Levitz-Katz, Lorraine; Klingberg, Gunilla; Lambert, Michele P; Marino, Bruno; Mascarenhas, Maria R; Moldenhauer, Julie; Moss, Edward M; Nowakowska, Beata Anna; Orchanian-Cheff, Ani; Putotto, Carolina; Repetto, Gabriela M; Schindewolf, Erica; Schneider, Maude; Solot, Cynthia B; Sullivan, Kathleen E; Swillen, Ann; Unolt, Marta; Van Batavia, Jason P; Vingerhoets, Claudia; Vorstman, Jacob; Bassett, Anne S; Mcdonald-Mcginn, Donna M - 01a Articolo in rivista
rivista: GENETICS IN MEDICINE (New York: Elsevier Inc.
Baltimore MD: Lippincott Williams & Wilkins) pp. 100338- - issn: 1530-0366 - wos: WOS:001029315800001 (6) - scopus: 2-s2.0-85146771243 (17)
11573/1682069 - 2023 -
Clinical variability in DYNC2H1-related skeletal ciliopathies includes Ellis-van Creveld syndrome Piceci-Sparascio, Francesca; Micale, Lucia; Torres, Barbara; Guida, Valentina; Consoli, Federica; Torrente, Isabella; Onori, Annamaria; Frustaci, Emanuela; D'asdia, Maria Cecilia; Petrizzelli, Francesco; Bernardini, Laura; Mancini, Cecilia; Soli, Fiorenza; Cocciadiferro, Dario; Guadagnolo, Daniele; Mastromoro, Gioia; Putotto, Carolina; Fontana, Franco; Brunetti-Pierri, Nicola; Novelli, Antonio; Pizzuti, Antonio; Marino, Bruno; Digilio, Maria Cristina; Mazza, Tommaso; Dallapiccola, Bruno; Ruiz-Perez, Victor Luis; Tartaglia, Marco; Castori, Marco; De Luca, Alessandro - 01a Articolo in rivista
rivista: EUROPEAN JOURNAL OF HUMAN GENETICS (-NATURE PUBLISHING GROUP, MACMILLAN BUILDING, 4 CRINAN ST, LONDON, ENGLAND, N1 9XW
-S Karger AG:Allschwilerstrasse 10, CH-4009 Basel Switzerland:011 41 61 3061111, EMAIL: orders@karger.ch, INTERNET: http://www.karger.com, Fax: 011 41 61 3061234) pp. 479-484 - issn: 1018-4813 - wos: WOS:000907881800003 (1) - scopus: 2-s2.0-85145605532 (3)
11573/1684176 - 2023 -
Cardiac function in adolescents and young adults with 22q11.2 deletion syndrome without congenital heart disease Putotto, Carolina; Unolt, Marta; Lambiase, Caterina; Marchetti, Flaminia; Anaclerio, Silvia; Favoriti, Alessandra; Tancredi, Giancarlo; Mastromoro, Gioia; Pugnaloni, Flaminia; Liberati, Natascia; De Luca, Enrica; Tarani, Luigi; De Canditiis, Daniela; Caputo, Viviana; Bernardini, Laura; Digilio, Maria Cristina; Marino, Bruno; Versacci, Paolo - 01a Articolo in rivista
rivista: EUROPEAN JOURNAL OF MEDICAL GENETICS (AMSTERDAM, NETHERLANDS,: ELSEVIER SCIENCE BV) pp. 104651- - issn: 1769-7212 - wos: WOS:000899351000013 (0) - scopus: 2-s2.0-85141768764 (0)
11573/1677571 - 2023 -
Transpositions of the great arteries versus aortic dextropositions. A review of some embryogenetic and morphological aspects Restivo, Angelo; Di Gioia, Cira Rosaria Tiziana; Marino Taussig De Bodonia, Bruno; Putotto, Carolina - 01g Articolo di rassegna (Review)
rivista: THE ANATOMICAL RECORD (Hoboken, NJ : John Wiley & Sons, 2007-) pp. 502-514 - issn: 1932-8486 - wos: WOS:000895829700001 (0) - scopus: 2-s2.0-85144067123 (0)
11573/1671730 - 2022 -
Social cognition impairments in 22q11.2DS individuals with and without psychosis: a comparison study with a large population of patients with schizophrenia Accinni, Tommaso; Buzzanca, Antonino; Frascarelli, Marianna; Carlone, Luca; Ghezzi, Francesco; Kotzalidis, Georgios D.; Bucci, Paola; Giordano, Giulia Maria; Girardi, Nicoletta; Panzera, Alessia; Montaldo, Simone; Fanella, Martina; Di Bonaventura, Carlo; Putotto, Carolina; Versacci, Paolo; Marino, Bruno; Pasquini, Massimo; Biondi, Massimo; Di Fabio, Fabio - 01a Articolo in rivista
rivista: SCHIZOPHRENIA BULLETIN OPEN (Cary NC: Oxford University Press) pp. 1-10 - issn: 2632-7899 - wos: (0) - scopus: 2-s2.0-85130703471 (4)
11573/1702826 - 2022 -
Single ventricle: amphibians and human beings Angelini, Paolo; Marino, Bruno; Corno, Antonio F. - 01a Articolo in rivista
rivista: WORLD JOURNAL OF PEDIATRICS (Press Hangzhou China) pp. 643-646 - issn: 1708-8569 - wos: WOS:000837505000001 (1) - scopus: 2-s2.0-85135712283 (1)
11573/1618403 - 2022 -
Clinical Manifestations of 22q11.2 Deletion Syndrome Cirillo, A.; Lioncino, M.; Maratea, A.; Passariello, A.; Fusco, A.; Fratta, F.; Monda, E.; Caiazza, M.; Signore, G.; Esposito, A.; Baban, A.; Versacci, P.; Putotto, C.; Marino, B.; Pignata, C.; Cirillo, E.; Giardino, G.; Sarubbi, B.; Limongelli, G.; Russo, M. G. - 01g Articolo di rassegna (Review)
rivista: HEART FAILURE CLINICS (Philadelphia : Saunders, c2005-) pp. 155-164 - issn: 1551-7136 - wos: WOS:000719585000015 (16) - scopus: 2-s2.0-85117920734 (22)
Corno, Antonio F.; Zhou, Zhen; Uppu, Santosh C.; Huang, Shuning; Marino, Bruno; Milewicz, Dianna M.; Salazar, Jorge D. - 01a Articolo in rivista
rivista: PEDIATRIC CARDIOLOGY (Springer-Verlag New York Incorporated:175 Fifth Avenue:New York, NY 10010:(212)460-1500, EMAIL: orders@springer-ny.com, INTERNET: http://www.springer-ny.com, Fax: (212)533-3503) pp. 1471-1480 - issn: 0172-0643 - wos: WOS:000769264700001 (5) - scopus: 2-s2.0-85126304516 (5)
11573/1618399 - 2022 -
Hypertrophic Cardiomyopathy in RASopathies: Diagnosis, Clinical Characteristics, Prognostic Implications, and Management Lioncino, M.; Monda, E.; Verrillo, F.; Moscarella, E.; Calcagni, G.; Drago, F.; Marino, B.; Digilio, M. C.; Putotto, C.; Calabro, P.; Russo, M. G.; Roberts, A. E.; Gelb, B. D.; Tartaglia, M.; Limongelli, G. - 01g Articolo di rassegna (Review)
rivista: HEART FAILURE CLINICS (Philadelphia : Saunders, c2005-) pp. 19-29 - issn: 1551-7136 - wos: WOS:000719585000004 (24) - scopus: 2-s2.0-85117832176 (29)
11573/1669249 - 2022 -
Crossed pulmonary arteries: An underestimated cardiovascular variant with a strong association with genetic syndromes{\textemdash}A report of 74 cases with systematic review of the literature Mastromoro, Gioia; Calcagni, Giulio; Vignaroli, Walter; Anaclerio, Silvia; Pugnaloni, Flaminia; Rinelli, Gabriele; Secinaro, Aurelio; Bordonaro, Veronica; Putotto, Carolina; Unolt, Marta; Cristina Digilio, Maria; Marino Taussig De Bodonia, Bruno; Versacci, Paolo - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS. PART A (WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030) pp. - - issn: 1552-4825 - wos: WOS:000789296400001 (4) - scopus: 2-s2.0-85129191379 (3)
11573/1660731 - 2022 -
COVID-19 Severity, Cardiological Outcome, and Immunogenicity of mRNA Vaccine on Adult Patients With 22q11.2 DS Pulvirenti, Federica; Mortari, Eva Piano; Putotto, Carolina; Terreri, Sara; Fernandez Salinas, Ane; Cinicola, Bianca Laura; Cimini, Eleonora; Di Napoli, Giulia; Sculco, Eleonora; Milito, Cinzia; Versacci, Paolo; Agrati, Chiara; Marino, Bruno; Carsetti, Rita; Quinti, Isabella - 01a Articolo in rivista
rivista: JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY. IN PRACTICE (Amsterdam [u.a.] : Elsevier) pp. - - issn: 2213-2198 - wos: WOS:000914945100001 (1) - scopus: 2-s2.0-85142845523 (1)
11573/1670969 - 2022 -
22q11.2 Deletion Syndrome. Impact of Genetics in the Treatment of Conotruncal Heart Defects Putotto, C.; Pugnaloni, F.; Unolt, M.; Maiolo, S.; Trezzi, M.; Digilio, M. C.; Cirillo, A.; Limongelli, G.; Marino, B.; Calcagni, G.; Versacci, P. - 01g Articolo di rassegna (Review)
rivista: CHILDREN (Basel: MDPI AG, 2014-) pp. 1-14 - issn: 2227-9067 - wos: WOS:000817704200001 (7) - scopus: 2-s2.0-85131526222 (8)
11573/1684184 - 2022 -
Anatomically corrected malposition of the great arteries (S,L,D) with mutation of Nodal gene Putotto, Carolina; Caruso, Elio; Marino Taussig De Bodonia, Bruno; Cristina Digilio, Maria; Novelli, Antonio; Agati, Salvatore - 01i Case report
rivista: CARDIOLOGY IN THE YOUNG (Greenwich Medical Media Limited:137 Euston Road, London NW1 2AA United Kingdom:011 44 20 73885444, INTERNET: http://www.greenwich-medical.co.uk, Fax: 011 44 20 86695891) pp. 1-3 - issn: 1047-9511 - wos: WOS:000798091500001 (0) - scopus: 2-s2.0-85165721619 (0)
11573/1664965 - 2022 -
Clinical Risk Factors for Aortic Root Dilation in Patients with 22q11.2 Deletion Syndrome: A Longitudinal Single-Center Study Putotto, Carolina; Pulvirenti, Federica; Pugnaloni, Flaminia; Isufi, Ina; Unolt, Marta; Anaclerio, Silvia; Caputo, Viviana; Bernardini, Laura; Messina, Elisa; Moretti, Corrado; Tarani, Luigi; Marino, Bruno; Versacci, Paolo - 01a Articolo in rivista
rivista: GENES (Basel : Molecular Diversity Preservation International) pp. 2334- - issn: 2073-4425 - wos: WOS:000902748800001 (0) - scopus: 2-s2.0-85144573205 (0)
11573/1569618 - 2021 -
Cardiac defects and genetic syndromes: old uncertainties and new insights Calcagni, G.; Pugnaloni, F.; Digilio, M. C.; Unolt, M.; Putotto, C.; Niceta, M.; Baban, A.; Sparascio, F. P.; Drago, F.; De Luca, A.; Tartaglia, M.; Marino, B.; Versacci, P. - 01g Articolo di rassegna (Review)
rivista: GENES (Basel : Molecular Diversity Preservation International) pp. 1047- - issn: 2073-4425 - wos: WOS:000677373200001 (11) - scopus: 2-s2.0-85110670442 (13)
11573/1618385 - 2021 -
Congenital heart defects in molecularly confirmed KBG syndrome patients Digilio, M. C.; Calcagni, G.; Gnazzo, M.; Versacci, P.; Dentici, M. L.; Capolino, R.; Sinibaldi, L.; Baban, A.; Putotto, C.; Alfieri, P.; Unolt, M.; Lepri, F. R.; Alesi, V.; Genovese, S.; Novelli, A.; Marino, B.; Dallapiccola, B. - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS. PART A (WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030) pp. - - issn: 1552-4825 - wos: WOS:000736707500001 (3) - scopus: 2-s2.0-85122498681 (4)
11573/1618338 - 2021 -
Anatomical substrate for biventricular repair in patients with left isomerism Madrigali, A.; Putotto, C.; Marino, B.; Versacci, P. - 01b Commento, Erratum, Replica e simili
rivista: ANNALS OF PEDIATRIC CARDIOLOGY (Mumbai : Medknow Publications) pp. 250-251 - issn: 0974-2069 - wos: WOS:000649437900027 (0) - scopus: 2-s2.0-85105717679 (0)
11573/1569620 - 2021 -
Smith–Magenis syndrome: Report of morphological and new functional cardiac findings with review of the literature Onesimo, R.; Versacci, P.; Delogu, A. B.; De Rosa, G.; Pugnaloni, F.; Blandino, R.; Leoni, C.; Calcagni, G.; Digilio, M. C.; Zollino, M.; Marino, B.; Zampino, G. - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS. PART A (WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030) pp. 2003-2011 - issn: 1552-4825 - wos: WOS:000636222400001 (1) - scopus: 2-s2.0-85103424357 (2)
11573/1486435 - 2021 -
Atrioventricular canal defect is the classic congenital heart disease in Bardet-Biedl syndrome Pugnaloni, Flaminia; Versacci, Paolo; Marino Taussig De Bodonia, Bruno; Cristina Digilio, Maria - 01m Editorial/Introduzione in rivista
rivista: ANNALS OF HUMAN GENETICS (-MALDEN, USA: WILEY-BLACKWELL PUBLISHING, INC
-Cambridge, United Kingdom: Cambridge University Press) pp. 101-102 - issn: 0003-4800 - wos: WOS:000606866000001 (3) - scopus: 2-s2.0-85099184388 (3)
11573/1618417 - 2021 -
Commentary: sVEGFR1 Is Enriched in Hepatic Vein Blood—Evidence for a Provisional Hepatic Factor Candidate? Putotto, C.; Marino, B.; Versacci, P. - 01b Commento, Erratum, Replica e simili
rivista: FRONTIERS IN PEDIATRICS (Lausanne : Frontiers Media S.A., 2013-) pp. 782779- - issn: 2296-2360 - wos: WOS:000721075400001 (0) - scopus: 2-s2.0-85119699868 (0)
11573/1486424 - 2020 -
Differences in morbidity and mortality in Down syndrome are related to the type of congenital heart defect Baban, A.; Olivini, N.; Cantarutti, N.; Cali, F.; Vitello, C.; Valentini, D.; Adorisio, R.; Calcagni, G.; Alesi, V.; Di Mambro, C.; Villani, A.; Dallapiccola, B.; Digilio, M. C.; Marino, B.; Carotti, A.; Drago, F. - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS. PART A (WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030) pp. 1342-1350 - issn: 1552-4825 - wos: WOS:000527387400001 (19) - scopus: 2-s2.0-85083774950 (17)
11573/1443519 - 2020 -
Atypical cardiac defects in patients with RASopathies: updated data on CARNET study Calcagni, G.; Gagliostro, G.; Limongelli, G.; Unolt, M.; De Luca, E.; Digilio, M. C.; Baban, A.; Albanese, S. B.; Ferrero, G. B.; Baldassarre, G.; Agnoletti, G.; Banaudi, E.; Marek, J.; Kaski, J. P.; Tuo, G.; Marasini, M.; Cairello, F.; Madrigali, A.; Pacileo, G.; Russo, M. G.; Milanesi, O.; Formigari, R.; Brighenti, M.; Ragni, L.; Donti, A.; Drago, F.; Dallapiccola, B.; Tartaglia, M.; Marino, B.; Versacci, P. - 01a Articolo in rivista
rivista: BIRTH DEFECTS RESEARCH (Hoboken N.J.: John Wiley & Sons Inc.) pp. 725-731 - issn: 2472-1727 - wos: WOS:000542696200004 (17) - scopus: 2-s2.0-85086579325 (16)
11573/1486440 - 2020 -
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion Cleynen, I.; Engchuan, W.; Hestand, M. S.; Heung, T.; Holleman, A. M.; Johnston, H. R.; Monfeuga, T.; Mcdonald-Mcginn, D. M.; Gur, R. E.; Morrow, B. E.; Swillen, A.; Vorstman, J. A. S.; Bearden, C. E.; Chow, E. W. C.; Van Den Bree, M.; Emanuel, B. S.; Vermeesch, J. R.; Warren, S. T.; Owen, M. J.; Chopra, P.; Cutler, D. J.; Duncan, R.; Kotlar, A. V.; Mulle, J. G.; Voss, A. J.; Zwick, M. E.; Diacou, A.; Golden, A.; Guo, T.; Lin, J. -R.; Wang, T.; Zhang, Z.; Zhao, Y.; Marshall, C.; Merico, D.; Jin, A.; Lilley, B.; Salmons, H. I.; Tran, O.; Holmans, P.; Pardinas, A.; Walters, J. T. R.; Demaerel, W.; Boot, E.; Butcher, N. J.; Costain, G. A.; Lowther, C.; Evers, R.; Van Amelsvoort, T. A. M. J.; Van Duin, E.; Vingerhoets, C.; Breckpot, J.; Devriendt, K.; Vergaelen, E.; Vogels, A.; Crowley, T. B.; Mcginn, D. E.; Moss, E. M.; Sharkus, R. J.; Unolt, M.; Zackai, E. H.; Calkins, M. E.; Gallagher, R. S.; Gur, R. C.; Tang, S. X.; Fritsch, R.; Ornstein, C.; Repetto, G. M.; Breetvelt, E.; Duijff, S. N.; Fiksinski, A.; Moss, H.; Niarchou, M.; Murphy, K. C.; Prasad, S. E.; Daly, E. M.; Gudbrandsen, M.; Murphy, C. M.; Murphy, D. G.; Buzzanca, A.; Fabio, F. D.; Digilio, M. C.; Pontillo, M.; Marino, B.; Vicari, S.; Coleman, K.; Cubells, J. F.; Ousley, O. Y.; Carmel, M.; Gothelf, D.; Mekori-Domachevsky, E.; Michaelovsky, E.; Weinberger, R.; Weizman, A.; Kushan, L.; Jalbrzikowski, M.; Armando, M.; Eliez, S.; Sandini, C.; Schneider, M.; Bena, F. S.; Antshel, K. M.; Fremont, W.; Kates, W. R.; Belzeaux, R.; Busa, T.; Philip, N.; Campbell, L. E.; Mccabe, K. L.; Hooper, S. R.; Schoch, K.; Shashi, V.; Simon, T. J.; Tassone, F.; Arango, C.; Fraguas, D.; Garcia-Minaur, S.; Morey-Canyelles, J.; Rosell, J.; Suner, D. H.; Raventos-Simic, J.; Epstein, M. P.; Williams, N. M.; Bassett, A. S. - 01a Articolo in rivista
rivista: MOLECULAR PSYCHIATRY (Nature Publishing Group:Brunel Road Houndmills, Basingstoke RG21 6XS United Kingdom:011 44 20 78334000, EMAIL: institutions@natureny.com, INTERNET: http://www.nature.com, Fax: 011 44 20 78434640) pp. - - issn: 1359-4184 - wos: WOS:000510821800003 (66) - scopus: 2-s2.0-85079175539 (70)
11573/1443511 - 2020 -
KBG syndrome: common and uncommon clinical features based on 31 new patients Gnazzo, M.; Lepri, F. R.; Dentici, M. L.; Capolino, R.; Pisaneschi, E.; Agolini, E.; Rinelli, M.; Alesi, V.; Versacci, P.; Genovese, S.; Cesario, C.; Sinibaldi, L.; Baban, A.; Bartuli, A.; Marino, B.; Cappa, M.; Dallapiccola, B.; Novelli, A.; Digilio, M. C. - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS. PART A (WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030) pp. 1073-1083 - issn: 1552-4825 - wos: WOS:000527011800015 (23) - scopus: 2-s2.0-85080997177 (22)
11573/1491566 - 2020 -
Common atrium/atrioventricular canal defect and postaxial polydactyly: a mild clinical subtype of Ellis-van Creveld syndrome caused by hypomorphic mutations in the EVC gene Piceci-Sparascio, F.; Palencia-Campos, A.; Soto-Bielicka, P.; D'anzi, A.; Guida, V.; Rosati, J.; Caparros-Martin, J. A.; Torrente, I.; D'asdia, M. C.; Versacci, P.; Briuglia, S.; Lapunzina, P.; Tartaglia, M.; Marino, B.; Digilio, M. C.; Ruiz-Perez, V. L.; De Luca, A. - 01a Articolo in rivista
rivista: HUMAN MUTATION (John Wiley & Sons Incorporated:Customer Service, 111 River Street:Hoboken, NJ 07030:(800)225-5945, (201)748-6000, EMAIL: societyinfo@wiley.com, INTERNET: http://www.wiley.com, Fax: (212)748-6551) pp. 2087-2093 - issn: 1059-7794 - wos: WOS:000577581400001 (6) - scopus: 2-s2.0-85092458649 (6)
11573/1443515 - 2020 -
Genetics of atrioventricular canal defects Pugnaloni, F.; Digilio, M. C.; Putotto, C.; De Luca, E.; Marino, B.; Versacci, P. - 01a Articolo in rivista
rivista: THE ITALIAN JOURNAL OF PEDIATRICS (London: BioMed Central Ltd. 2008-
-Pacini Editore) pp. 61- - issn: 1720-8424 - wos: WOS:000536294400003 (8) - scopus: 2-s2.0-85084627783 (6)
11573/1474798 - 2020 -
Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects Zhao, Y.; Diacou, A.; Johnston, H. R.; Musfee, F. I.; Mcdonald-Mcginn, D. M.; Mcginn, D.; Crowley, T. B.; Repetto, G. M.; Swillen, A.; Breckpot, J.; Vermeesch, J. R.; Kates, W. R.; Digilio, M. C.; Unolt, M.; Marino, B.; Pontillo, M.; Armando, M.; Di Fabio, Fabio; Vicari, S.; Van Den Bree, M.; Moss, H.; Owen, M. J.; Murphy, K. C.; Murphy, C. M.; Murphy, D.; Schoch, K.; Shashi, V.; Tassone, F.; Simon, T. J.; Shprintzen, R. J.; Campbell, L.; Philip, N.; Heine-Suner, D.; Garcia-Minaur, S.; Fernandez, L.; Antonarakis, S. E.; Biondi, M.; Boot, E.; Breetvelt, E.; Busa, T.; Butcher, N.; Buzzanca, A.; Carmel, M.; Cleynen, I.; Cutler, D.; Dallapiccola, B.; De La Fuente Sanches, M. A.; Epstein, M. P.; Evers, R.; Fernandez, L.; Fritsch, R.; Algas, F. G.; Guo, T.; Gur, R.; Hestand, M. S.; Heung, T.; Hooper, S.; Jin, A.; Kushan-Wells, L.; Laorden-Nieto, A. T.; Lattanzi, G.; Marshall, C.; Mccabe, K.; Michaelovsky, E.; Ornstein, C.; Silversides, C.; Tran, O.; Van Duin, E. D. A.; Vergaelen, E.; Warren, S. T.; Weinberger, R.; Weizman, A.; Zhang, Z.; Zwick, M.; Bearden, C. E.; Vingerhoets, C.; Van Amelsvoort, T.; Eliez, S.; Schneider, M.; Vorstman, J. A. S.; Gothelf, D.; Zackai, E.; Agopian, A. J.; Gur, R. E.; Bassett, A. S.; Emanuel, B. S.; Goldmuntz, E.; Mitchell, L. E.; Wang, T.; Morrow, B. E. - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF HUMAN GENETICS (University of Chicago Press:PO Box 37005, Journals Division:Chicago, IL 60637:(877)705-1878, (877)705-1878, (773)753-2247, EMAIL: subscriptions@press.uchicago.edu, INTERNET: http://www.press.uchicago.edu, Fax: (877)705-1879, (773)753-0811) pp. 26-40 - issn: 0002-9297 - wos: WOS:000505170800003 (34) - scopus: 2-s2.0-85077046877 (41)
11573/1349935 - 2019 -
Pediatric patients with RASopathy-associated hypertrophic cardiomyopathy: the multifaceted consequences of PTPN11 mutations Calcagni, G.; Digilio, M. C.; Marino, B.; Tartaglia, M. - 01b Commento, Erratum, Replica e simili
rivista: ORPHANET JOURNAL OF RARE DISEASES (London : BioMed Central) pp. - - issn: 1750-1172 - wos: WOS:000474612800004 (5) - scopus: 2-s2.0-85069269514 (6)
11573/1184820 - 2019 -
Atrioventricular canal defect and genetic syndromes: the unifying role of sonic hedgehog Digilio, M C; Pugnaloni, F; De Luca, A; Calcagni, G; Baban, A; Dentici, M L; Versacci, P; Dallapiccola, B; Tartaglia, M; Marino, B - 01g Articolo di rassegna (Review)
rivista: CLINICAL GENETICS (Oxford : Blackwell) pp. 268-276 - issn: 1399-0004 - wos: WOS:000455527300009 (17) - scopus: 2-s2.0-85047490590 (22)
11573/1349948 - 2019 -
Atrioventricular canal defect as partial expression of heterotaxia in patients with Bardet-Biedl syndrome Digilio, M Cristina; Calcagni, Giulio; De Luca, Alessandro; Guida, Valentina; Marino, Bruno - 01b Commento, Erratum, Replica e simili
rivista: THE JOURNAL OF PEDIATRICS (New York NY: Elsevier
St. Louis Mo.: C.V. Mosby) pp. - - issn: 0022-3476 - wos: WOS:000514853200059 (3) - scopus: 2-s2.0-85079240522 (3)
11573/1347974 - 2019 -
Familial aggregation of “apple peel” intestinal atresia and cardiac left-sided obstructive lesions: a possible causal relationship with NOTCH1 gene mutations Digilio, M. C.; Magliozzi, M.; Di Pede, A.; Valfre, L.; Dentici, M. L.; Auriti, C.; Marino, B.; Novelli, A.; Dallapiccola, B. - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS. PART A (WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030) pp. 1570-1574 - issn: 1552-4825 - wos: WOS:000478591600026 (1) - scopus: 2-s2.0-85066111917 (1)
11573/1260652 - 2019 -
Left pulmonary artery in 22q11.2 deletion syndrome. Echocardiographic evaluation in patients without cardiac defects and role of Tbx1 in mice. Mastromoro, Gioia; Calcagni, Giulio; Versacci, Paolo; Putotto, Carolina; Chinali, Marcello; Lambiase, Caterina; Unolt, Marta; Pelliccione, Elena; Anaclerio, Silvia; Caprio, Cinzia; Cioffi, Sara; Bilio, Marchesa; Baban, Anwar; Drago, Fabrizio; Cristina Digilio, Maria; Marino Taussig De Bodonia, Bruno; Baldini, Antonio - 01a Articolo in rivista
rivista: PLOS ONE (San Francisco, CA : Public Library of Science) pp. - - issn: 1932-6203 - wos: WOS:000462867000004 (10) - scopus: 2-s2.0-85063658968 (12)
11573/1310020 - 2019 -
Prevalence, type, and molecular spectrum of NF1 mutations in patients with neurofibromatosis type 1 and congenital heart disease Pinna, Valentina; Daniele, Paola; Calcagni, Giulio; Mariniello, Lucio; Criscione, Roberta; Giardina, Chiara; Lepri, Francesca Romana; Hozhabri, Hossein; Alberico, Angela; Cavone, Stefania; Morella, Annunziata Tina; Mandile, Roberta; Annunziata, Francesca; Di Giosaffatte, Niccolò; D'asdia, Maria Cecilia; Versacci, Paolo; Capolino, Rossella; Strisciuglio, Pietro; Giustini, Sandra; Melis, Daniela; Digilio, Maria Cristina; Tartaglia, Marco; Marino, Bruno; De Luca, Alessandro - 01a Articolo in rivista
rivista: GENES (Basel : Molecular Diversity Preservation International) pp. - - issn: 2073-4425 - wos: WOS:000487954700065 (14) - scopus: 2-s2.0-85071740488 (19)
11573/1278929 - 2018 -
Impact of genetic studies on comprehension and treatment of congenital heart disease Alicandro, Tatiana; Putotto, Carolina; Calcagni, Giulio; Unolt, Marta; Mastromoro, Gioia; Digilio, Maria Cristina; Versacci, Paolo; Marino, Bruno - 01a Articolo in rivista
rivista: PROGRESS IN PEDIATRIC CARDIOLOGY (Reading, MA : Andover Medical Publishers, c1992-) pp. 31-36 - issn: 1058-9813 - wos: WOS:000451752200006 (0) - scopus: 2-s2.0-85056477576 (1)
11573/1195895 - 2018 -
Long-term survival and phenotypic spectrum in heterotaxy syndrome: a 25-year follow-up experience Baban, Anwar; Cantarutti, Nicoletta; Adorisio, Rachele; Lombardi, Roberta; Calcagni, Giulio; Piano Mortari, Eva; Dallapiccola, Bruno; Marino, Bruno; Iorio, Fiore Salvatore; Carsetti, Rita; Digilio, Maria Cristina; Giannico, Salvatore; Drago, Fabrizio; Carotti, Adriano - 01a Articolo in rivista
rivista: INTERNATIONAL JOURNAL OF CARDIOLOGY (Elsevier Science Ireland Limited:PO Box 85, Limerick Ireland:011 353 61 709600, 011 353 61 61944, EMAIL: usinfo-f@elsevier.com, INTERNET: http://www.elsevier.com, Fax: 011 353 61 709114) pp. 100-105 - issn: 0167-5273 - wos: WOS:000439363400027 (22) - scopus: 2-s2.0-85050085948 (24)
11573/1192465 - 2018 -
Clinical presentation and natural history of hypertrophic cardiomyopathy in RASopathies Calcagni, Giulio; Adorisio, Rachele; Martinelli, Simone; Grutter, Giorgia; Baban, Anwar; Versacci, Paolo; Digilio, Maria Cristina; Drago, Fabrizio; Gelb, Bruce D.; Tartaglia, Marco; Marino, Bruno - 01a Articolo in rivista
rivista: HEART FAILURE CLINICS (Philadelphia : Saunders, c2005-) pp. 225-235 - issn: 1551-7136 - wos: WOS:000427567000011 (39) - scopus: 2-s2.0-85043401035 (43)
11573/1260660 - 2018 -
Data on cardiac defects, morbidity and mortality in patients affected by RASopathies. CARNET study results Calcagni, Giulio; Limongelli, Giuseppe; D'ambrosio, Angelo; Gesualdo, Francesco; Digilio, Maria Cristina; Baban, Anwar; Albanese, Sonia B.; Versacci, Paolo; De Luca, Enrica; Ferrero, Giovanni B.; Baldassarre, Giuseppina; Agnoletti, Gabriella; Banaudi, Elena; Marek, Jan; Kaski, Juan P.; Tuo, Giulia; Russo, Maria Giovanna; Pacileo, Giuseppe; Milanesi, Ornella; Messina, Daniela; Marasini, Maurizio; Cairello, Francesca; Formigari, Roberto; Brighenti, Maurizio; Dallapiccola, Bruno; Tartaglia, Marco; Marino, Bruno - 01a Articolo in rivista
rivista: DATA IN BRIEF (New York : Elsevier Inc.) pp. 649-654 - issn: 2352-3409 - wos: WOS:000449758500088 (2) - scopus: 2-s2.0-85037983251 (6)
11573/1343159 - 2018 -
Partial atrioventricular septal defect in infancy: Don't we need to know more? Di Carlo, D.; Putotto, C.; Marino, B. - 01f Lettera, Nota
rivista: HEART (BMJ / British Medical Journal Publishing Group:PO Box 299, London WC1H 9TD United Kingdom:011 44 20 73836270, EMAIL: subscriptions@bmjgroup.com, INTERNET: http://www.bmjpg.com/bmj, Fax: 011 44 20 73836402) pp. 1470-1470 - issn: 1355-6037 - wos: WOS:000445082000016 (1) - scopus: 2-s2.0-85052856426 (0)
11573/1192500 - 2018 -
Late arrhytmias after repair of atrioventricular septal defect: Down's Syndrome is not the culprit Di Carlo, Duccio; Marino, Bruno - 01m Editorial/Introduzione in rivista
rivista: INTERNATIONAL JOURNAL OF CARDIOLOGY (Elsevier Science Ireland Limited:PO Box 85, Limerick Ireland:011 353 61 709600, 011 353 61 61944, EMAIL: usinfo-f@elsevier.com, INTERNET: http://www.elsevier.com, Fax: 011 353 61 709114) pp. 162-163 - issn: 0167-5273 - wos: WOS:000424514800036 (0) - scopus: 2-s2.0-85041663357 (0)
11573/1325539 - 2018 -
Surgery for Complex forms of Atrioventricular Septal Defect: Early Survival and Probability of Cure Di Carlo, Duccio; Putotto, Carolina; Versacci, Paolo; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: JOURNAL OF RARE DISORDERS. DIAGNOSIS & THERAPY (Wilmington, Delaware: iMedPub, 2015-) pp. 1-7 - issn: 2380-7245 - wos: (0) - scopus: (0)
11573/1282000 - 2018 -
Heterozygous missense mutations in NFATC1 are associated with atrioventricular septal defect Ferese, R.; Bonetti, M.; Consoli, F.; Guida, V.; Sarkozy, A.; Lepri, F. R.; Versacci, P.; Gambardella, S.; Calcagni, G.; Margiotti, K.; Piceci Sparascio, F.; Hozhabri, H.; Mazza, T.; Digilio, M. C.; Dallapiccola, B.; Tartaglia, M.; Hertog, J. D.; De Luca, A.; Marino, Bruno - 01a Articolo in rivista
rivista: HUMAN MUTATION (John Wiley & Sons Incorporated:Customer Service, 111 River Street:Hoboken, NJ 07030:(800)225-5945, (201)748-6000, EMAIL: societyinfo@wiley.com, INTERNET: http://www.wiley.com, Fax: (212)748-6551) pp. 1428-1441 - issn: 1059-7794 - wos: WOS:000444948000014 (14) - scopus: 2-s2.0-85051056677 (14)
11573/1193929 - 2018 -
Biallelic mutations in DYNC2LI1 are a rare cause of Ellis-van Creveld syndrome Niceta, M.; Margiotti, K.; Digilio, M. C.; Guida, V.; Bruselles, A.; Pizzi, S.; Ferraris, A.; Memo, L.; Laforgia, N.; Dentici, M. L.; Consoli, F.; Torrente, I.; Ruiz-Perez, V. L.; Dallapiccola, B.; Marino, B.; De Luca, A.; Tartaglia, M. - 01a Articolo in rivista
rivista: CLINICAL GENETICS (Blackwell Munksgaard:PO Box 2148, Periodicals Department, DK-1016 Copenhagen K Denmark:011 45 33 755913, EMAIL: agentservices@oxon.blackwellpublishing.com, INTERNET: http://www.blackwellmunksgaard.com, Fax: 011 45 77 333377) pp. 632-639 - issn: 0009-9163 - wos: WOS:000426255400021 (20) - scopus: 2-s2.0-85041074318 (19)
11573/1195893 - 2018 -
Primary lymphedema and other lymphatic anomalies are associated with 22q11.2 deletion syndrome Unolt, Marta; Barry, Jessica; Digilio, Maria Cristina; Marino, Bruno; Bassett, Anne; Oechslin, Erwin; Low, David W.; Belasco, Jean B.; Kallish, Staci; Sullivan, Kathleen; Zackai, Elaine H.; Mcdonald-Mcginn, Donna M. - 01a Articolo in rivista
rivista: EUROPEAN JOURNAL OF MEDICAL GENETICS (AMSTERDAM, NETHERLANDS,: ELSEVIER SCIENCE BV) pp. 411-415 - issn: 1769-7212 - wos: WOS:000434478700010 (3) - scopus: 2-s2.0-85041921550 (3)
11573/1119509 - 2018 -
Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiers Unolt, Marta; Versacci, Paolo; Anaclerio, Silvia; Lambiase, Caterina; Calcagni, Giulio; Trezzi, Matteo; Carotti, Adriano; Crowley, Terrence Blaine; Zackai, Elaine H.; Goldmuntz, Elizabeth; Gaynor, James William; Digilio, Maria Cristina; Mcdonald-Mcginn, Donna M.; Marino, Bruno - 01g Articolo di rassegna (Review)
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS. PART A (WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030) pp. 2087-2098 - issn: 1552-4825 - wos: WOS:000449718500008 (37) - scopus: 2-s2.0-85045704286 (46)
Versacci, Paolo; Di Carlo, Duccio; Digilio, Maria C; Marino, Bruno - 01g Articolo di rassegna (Review)
rivista: CURRENT OPINION IN PEDIATRICS (Lippincott, Williams & Wilkins:530 Walnut Street:Philadelphia, PA 19106:(800)638-3030, (301)223-2300, EMAIL: orders@lww.com, INTERNET: http://www.lww.com, Fax: (301)223-2320, (301)223-2320) pp. 616-622 - issn: 1040-8703 - wos: WOS:000457806500004 (43) - scopus: 2-s2.0-85056626557 (51)
11573/1119505 - 2018 -
Some Isolated Cardiac Malformations Can Be Related to Laterality Defects Versacci, Paolo; Pugnaloni, Flaminia; Digilio, Maria Cristina; Putotto, Carolina; Unolt, Marta; Calcagni, Giulio; Baban, Anwar; Marino, Bruno - 01a Articolo in rivista
rivista: JOURNAL OF CARDIOVASCULAR DEVELOPMENT AND DISEASE (Basel : MDPI AG, 2014-) pp. 24- - issn: 2308-3425 - wos: WOS:000455161100006 (13) - scopus: 2-s2.0-85056738425 (13)
11573/1022634 - 2017 -
Cardiac defects, morbidity and mortality in patients affected by RASopathies. CARNET study results Calcagni, Giulio; Limongelli, Giuseppe; D'ambrosio, Angelo; Gesualdo, Francesco; Digilio, M. Cristina; Baban, Anwar; Albanese, Sonia B.; Versacci, Paolo; De Luca, Enrica; Ferrero, Giovanni B.; Baldassarre, Giuseppina; Agnoletti, Gabriella; Banaudi, Elena; Marek, Jan; Kaski, Juan P.; Tuo, Giulia; Russo, M. Giovanna; Pacileo, Giuseppe; Milanesi, Ornella; Messina, Daniela; Marasini, Maurizio; Cairello, Francesca; Formigari, Roberto; Brighenti, Maurizio; Dallapiccola, Bruno; Tartaglia, Marco; Marino, Bruno - 01a Articolo in rivista
rivista: INTERNATIONAL JOURNAL OF CARDIOLOGY (Elsevier Science Ireland Limited:PO Box 85, Limerick Ireland:011 353 61 709600, 011 353 61 61944, EMAIL: usinfo-f@elsevier.com, INTERNET: http://www.elsevier.com, Fax: 011 353 61 709114) pp. 92-98 - issn: 0167-5273 - wos: WOS:000411288700017 (57) - scopus: 2-s2.0-85026384839 (60)
11573/1119513 - 2017 -
Congenital heart disease and genetic syndromes: new insights into molecular mechanisms Calcagni, Giulio; Unolt, Marta; Digilio, Maria Cristina; Baban, Anwar; Versacci, Paolo; Tartaglia, Marco; Baldini, Antonio; Marino, Bruno - 01g Articolo di rassegna (Review)
rivista: EXPERT REVIEW OF MOLECULAR DIAGNOSTICS (--London, United Kingdom: Expert Reviews Ltd
-London : Future Drugs, 2001-) pp. 861-870 - issn: 1473-7159 - wos: WOS:000422748900007 (37) - scopus: 2-s2.0-85027331602 (38)
11573/1193951 - 2017 -
Congenital heart defects in molecularly proven Kabuki syndrome patients Digilio, Maria Cristina; Gnazzo, Maria; Lepri, Francesca; Dentici, Maria Lisa; Pisaneschi, Elisa; Baban, Anwar; Passarelli, Chiara; Capolino, Rossella; Angioni, Adriano; Novelli, Antonio; Marino, Bruno; Dallapiccola, Bruno - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS. PART A (WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030) pp. 2912-2922 - issn: 1552-4825 - wos: WOS:000413425400007 (51) - scopus: 2-s2.0-85028979213 (58)
11573/1193960 - 2017 -
Genome-wide association study to find modifiers for tetralogy of fallot in the 22q11.2 deletion syndrome identifies variants in the GPR98 locus on 5q14.3 Guo, Tingwei; Repetto, Gabriela M.; Mcdonald Mcginn, Donna M.; Chung, Jonathan H.; Nomaru, Hiroko; Campbell, Christopher L.; Blonska, Anna; Bassett, Anne S.; Chow, Eva W. C.; Mlynarski, Elisabeth E.; Swillen, Ann; Vermeesch, Joris; Devriendt, Koen; Gothelf, Doron; Carmel, Miri; Michaelovsky, Elena; Schneider, Maude; Eliez, Stephan; Antonarakis, Stylianos E.; Coleman, Karlene; Tomita-Mitchell, Aoy; Mitchell, Michael E.; Digilio, M. Cristina; Dallapiccola, Bruno; Marino, Bruno; Philip, Nicole; Busa, Tiffany; Kushan-Wells, Leila; Bearden, Carrie E.; Piotrowicz, Małgorzata; Hawuła, Wanda; Roberts, Amy E.; Tassone, Flora; Simon, Tony J.; Van Duin, Esther D. A.; Van Amelsvoort, Thérèse A.; Kates, Wendy R.; Zackai, Elaine; Johnston, H. Richard; Cutler, David J.; Agopian, A. J.; Goldmuntz, Elizabeth; Mitchell, Laura E.; Wang, Tao; Emanuel, Beverly S.; Morrow, Bernice E. - 01a Articolo in rivista
rivista: CIRCULATION, CARDIOVASCULAR GENETICS (Philadelphia, PA : Lippincott Williams & Wilkins) pp. - - issn: 1942-325X - wos: WOS:000424292400004 (17) - scopus: 2-s2.0-85032884386 (19)
11573/958623 - 2016 -
Direct cerebral perfusion and cooling in experimental cardiac arrest Bellomo, Rinaldo; Marino Taussig De Bodonia, Bruno; Angelopoulos, Peter; Carson, Scott; Eastwood, Glenn; Kosaka, Junko; Iguchi, Naoya; Hilton, Andrew; May, Clive - 01a Articolo in rivista
rivista: CRITICAL CARE AND RESUSCITATION (Bedford Park, S. Aust.: Australasian Academy of Critical Care Medicine 1999-) pp. 255-260- - issn: 1441-2772 - wos: WOS:000389870700008 (0) - scopus: 2-s2.0-85007286323 (0)
11573/973481 - 2016 -
Congenital heart defects in Noonan syndrome and RIT1 mutation Calcagni, Giulio; Baban, Anwar; Lepri, Francesca Romana; Marino Taussig De Bodonia, Bruno; Tartaglia, Marco; Digilio, Maria Cristina - 01f Lettera, Nota
rivista: GENETICS IN MEDICINE (New York: Elsevier
Baltimore MD: Williams & Wilkins) pp. 1320-1320 - issn: 1098-3600 - wos: WOS:000389563700024 (13) - scopus: 2-s2.0-85000399426 (15)
11573/958610 - 2016 -
What Is New in Genetics of Congenital Heart Defects? Digilio, Maria Cristina; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: FRONTIERS IN PEDIATRICS (Lausanne : Frontiers Media S.A., 2013-) pp. 120- - issn: 2296-2360 - wos: WOS:000388984100001 (21) - scopus: 2-s2.0-85027028891 (21)
11573/958697 - 2016 -
Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndrome Mlynarski, Elisabeth E.; Xie, Michael; Taylor, Deanne; Sheridan, Molly B.; Guo, Tingwei; Racedo, Silvia E.; Mcdonald Mcginn, Donna M.; Chow, Eva W. C.; Vorstman, Jacob; Swillen, Ann; Devriendt, Koen; Breckpot, Jeroen; Digilio, Maria Cristina; Marino Taussig De Bodonia, Bruno; Dallapiccola, Bruno; Philip, Nicole; Simon, Tony J.; Roberts, Amy E.; Piotrowicz, Małgorzata; Bearden, Carrie E.; Eliez, Stephan; Gothelf, Doron; Coleman, Karlene; Kates, Wendy R.; Devoto, Marcella; Zackai, Elaine; Heine Suñer, Damian; Goldmuntz, Elizabeth; Bassett, Anne S.; Morrow, Bernice E.; Emanuel, Beverly S. - 01a Articolo in rivista
rivista: HUMAN GENETICS (Germany: Springer Verlag Germany) pp. 273-285 - issn: 0340-6717 - wos: WOS:000370818800002 (29) - scopus: 2-s2.0-84958770521 (28)
11573/973585 - 2016 -
Sprengel anomaly in deletion 22q11.2 (DiGeorge/Velo-Cardio-Facial) syndrome Radio, Francesca Clementina; Digilio, Maria Cristina; Capolino, Rossella; Dentici, Maria Lisa; Unolt, Marta; Alesi, Viola; Novelli, Antonio; Marino Taussig De Bodonia, Bruno; Dallapiccola, Bruno - 01i Case report
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS. PART A (WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030) pp. 661-664 - issn: 1552-4825 - wos: WOS:000373098900016 (1) - scopus: 2-s2.0-84959526468 (4)
Versacci, P.; Vignaroli, W.; Mastromoro, G.; Ventriglia, F.; Marino, B. - 02a Capitolo o Articolo
libro: Fetal and Hybrid Procedures in Congenital Heart Diseases - (978-3-319-40086-0; 978-3-319-40088-4)
11573/1193935 - 2015 -
Hypoplastic left heart syndrome and 21q22.3 deletion Ciocca, Laura; Digilio, M. Cristina; Lombardo, Antonietta; D'elia, Gemma; Baban, Anwar; Capolino, Rossella; Petrocchi, Stefano; Russo, Serena; Sirleto, Pietro; Roberti, M. Cristina; Marino, Bruno; Angioni, Adriano; Dallapiccola, Bruno - 01i Case report
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS. PART A (WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030) pp. 579-586 - issn: 1552-4825 - wos: WOS:000350283400013 (8) - scopus: 2-s2.0-84923005238 (8)
11573/856664 - 2015 -
Left ventricular non compaction with aortic valve anomalies: A recurrent feature of 22q11.2 distal deletion syndrome Digilio, M. Cristina; Versacci, Paolo; Bernardini, Laura; Novelli, Antonio; Marino Taussig De Bodonia, Bruno; Dallapiccola, Bruno - 01f Lettera, Nota
rivista: EUROPEAN JOURNAL OF MEDICAL GENETICS (AMSTERDAM, NETHERLANDS,: ELSEVIER SCIENCE BV) pp. 406-408 - issn: 1769-7212 - wos: WOS:000358788600008 (1) - scopus: 2-s2.0-84938251319 (1)
Mcdonald-Mcginn, Donna M.; Sullivan, Kathleen E.; Marino, Bruno; Philip, Nicole; Swillen, Ann; Vorstman, Jacob A. S.; Zackai, Elaine H.; Emanuel, Beverly S.; Vermeesch, Joris R.; Morrow, Bernice E.; Scambler, Peter J.; Bassett, Anne S. - 01g Articolo di rassegna (Review)
rivista: NATURE REVIEWS. DISEASE PRIMERS (London : Nature Publishing Group) pp. - - issn: 2056-676X - wos: WOS:000381348900001 (642) - scopus: 2-s2.0-85017227463 (734)
11573/788381 - 2015 -
Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion Syndrome Mlynarski, Elisabeth E; Sheridan, Molly B; Xie, Michael; Guo, Tingwei; Racedo, Silvia E; Mcdonald Mcginn, Donna M; Gai, Xiaowu; Chow, Eva W. C; Vorstman, Jacob; Swillen, Ann; Devriendt, Koen; Breckpot, Jeroen; Digilio, Maria Cristina; Marino Taussig De Bodonia, Bruno; Dallapiccola, Bruno; Philip, Nicole; Simon, Tony J; Roberts, Amy E; Piotrowicz, Małgorzata; Bearden, Carrie E; Eliez, Stephan; Gothelf, Doron; Coleman, Karlene; Kates, Wendy R; Devoto, Marcella; Zackai, Elaine; Heine Suñer, Damian; Shaikh, Tamim H; Bassett, Anne S; Goldmuntz, Elizabeth; Morrow, Bernice E; Emanuel, Beverly S. - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF HUMAN GENETICS (University of Chicago Press:PO Box 37005, Journals Division:Chicago, IL 60637:(877)705-1878, (877)705-1878, (773)753-2247, EMAIL: subscriptions@press.uchicago.edu, INTERNET: http://www.press.uchicago.edu, Fax: (877)705-1879, (773)753-0811) pp. 753-64-764 - issn: 0002-9297 - wos: WOS:000354189300006 (55) - scopus: 2-s2.0-84929282777 (61)
11573/1291546 - 2015 -
DETECTION OF CARDIOVASCULAR ABNORMALITIES IN PEDIATRIC PATIENTS WITH EHLERS-DANLOS SYNDROME: ROLE OF NEW ECHOCARDIOGRAPHIC TECHNIQUES Vignaroli, W; Mastromoro, G; Camerota, F; Celletti, C; Celli, M; Turchetti, A; Zambrano, A; Marino, B; Versacci, P - 04d Abstract in atti di convegno
rivista: GIORNALE ITALIANO DI CARDIOLOGIA (ROMA: Il Pensiero Scientifico
Roma : C.E.P.I. Centro editoriale pubblicitario italiano) pp. 17s-51s - issn: 1972-6481 - wos: (0) - scopus: (0)
congresso: XLV CONGRESSO NAZIONALE della Societa' Italiana di Cardiologia Pediatrica e delle Cardiopatie Congenite (Napoli)
libro: Giornale Italiano di Cardiologia - ()
11573/980476 - 2014 -
Clinical features and follow-up in patients with 22q11.2 deletion syndrome Cancrini, Caterina; Puliafito, Pamela; Digilio, Maria Cristina; Soresina, Annarosa; Martino, Silvana; Rondelli, Roberto; Consolini, Rita; Ruga, Ezia Maria; Cardinale, Fabio; Finocchi, Andrea; Romiti, Maria Luisa; Martire, Baldassarre; Bacchetta, Rosa; Albano, Veronica; Carotti, Adriano; Specchia, Fernando; Montin, Davide; Cirillo, Emilia; Cocchi, Guido; Trizzino, Antonino; Bossi, Grazia; Milanesi, Ornella; Azzari, Chiara; Corsello, Giovanni; Pignata, Claudio; Aiuti, Alessandro; Pietrogrande, Maria Cristina; Ugazio, Alberto Giovanni; Plebani, Alessandro; Rossi, Paolo; Italian Network For Primary, Immunodeficiencies; Marino Taussig De Bodonia, Bruno; Quinti, Isabella - 01a Articolo in rivista
rivista: THE JOURNAL OF PEDIATRICS (New York NY: Elsevier
St. Louis Mo.: C.V. Mosby) pp. 1475-1480 - issn: 0022-3476 - wos: WOS:000336503200046 (94) - scopus: 2-s2.0-84901480908 (100)
11573/561074 - 2014 -
Challenges of classifying double outlet right ventricle: Importance for genotype-phenotype analyses. Silvestri, Lucia Martina; A., Scarabotti; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS. PART A (WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030) pp. 1340-1340 - issn: 1552-4825 - wos: WOS:000334290300044 (0) - scopus: 2-s2.0-84898882791 (0)
11573/561073 - 2014 -
Surgical Outcomes for Patients with Turner Syndrome. Versacci, Paolo; Silvestri, Lucia Martina; Maiolo, Stella; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: PEDIATRIC CARDIOLOGY (Springer-Verlag New York Incorporated:175 Fifth Avenue:New York, NY 10010:(212)460-1500, EMAIL: orders@springer-ny.com, INTERNET: http://www.springer-ny.com, Fax: (212)533-3503) pp. - - issn: 0172-0643 - wos: WOS:000339112400028 (0) - scopus: 2-s2.0-84904697652 (0)
11573/759245 - 2013 -
Association of Di George anomaly and caudal dysplasia sequence in neonate born to a diabetic mother. Dentici, Ml; Placidi, S; Francalanci, P; Capolino, R; Rinelli, G; Marino Taussig De Bodonia, Bruno; Digilio, Mc; Dalla Piccola, Bruno - 01b Commento, Erratum, Replica e simili
rivista: CARDIOLOGY IN THE YOUNG (Greenwich Medical Media Limited:137 Euston Road, London NW1 2AA United Kingdom:011 44 20 73885444, INTERNET: http://www.greenwich-medical.co.uk, Fax: 011 44 20 86695891) pp. 14-17 - issn: 1047-9511 - wos: WOS:000314424300003 (1) - scopus: 2-s2.0-84873383315 (2)
11573/759246 - 2013 -
Congenital heart defects in recurrent reciprocal 1q21.1 deletion and duplication syndromes: rare association with pulmonary valve stenosis Digilio, Mc; Bernardini, L; Consoli, F; Lepri, Fr; Giuffrida, Mg; Baban, A; Surace, C; Ferese, R; Angioni, A; Novelli, A; Marino Taussig De Bodonia, Bruno; De Luca, A; Dallapiccola, A. - 01i Case report
rivista: EUROPEAN JOURNAL OF MEDICAL GENETICS (AMSTERDAM, NETHERLANDS,: ELSEVIER SCIENCE BV) pp. 144-149 - issn: 1769-7212 - wos: WOS:000324892400004 (28) - scopus: 2-s2.0-84874319887 (30)
11573/759247 - 2013 -
Syndromic non-compaction of the left ventricle: associated chromosomal anomalies Digilio, Mc; Bernardini, L; Gagliardi, Mg; Versacci, P; Baban, A; Capolino, R; Dentici, Ml; Roberti, Mc; Angioni, A; Novelli, A; Marino Taussig De Bodonia, Bruno; Dalla Piccola, Bruno - 01a Articolo in rivista
rivista: CLINICAL GENETICS (Oxford : Blackwell) pp. 362-367 - issn: 1399-0004 - wos: WOS:000324297800011 (20) - scopus: 2-s2.0-84883830157 (22)
11573/759242 - 2013 -
A variant in the carboxyl-terminus of connexin 40 alters GAP junctions and increases risk for tetralogy of Fallot Guida, V; Ferese, R; Rocchetti, M; Bonetti, M; Sarkozy, A; Cecchetti, S; Gelmetti, V; Lepri, F; Copetti, M; Lamorte, G; Digilio, Mc; Marino Taussig De Bodonia, Bruno; Zaza, A; Den Hertog, J; Dalla Piccola, Bruno; De Luca, A. - 01a Articolo in rivista
rivista: EUROPEAN JOURNAL OF HUMAN GENETICS (-NATURE PUBLISHING GROUP, MACMILLAN BUILDING, 4 CRINAN ST, LONDON, ENGLAND, N1 9XW
-S Karger AG:Allschwilerstrasse 10, CH-4009 Basel Switzerland:011 41 61 3061111, EMAIL: orders@karger.ch, INTERNET: http://www.karger.com, Fax: 011 41 61 3061234) pp. 69-75 - issn: 1018-4813 - wos: WOS:000312492500015 (33) - scopus: 2-s2.0-84871255563 (35)
11573/560045 - 2013 -
Novel and recurrent EVC and EVC2 mutations in Ellis-van Creveld syndrome and Weyers acrofacial dyostosis Maria Cecilia, D'asdia; Isabella, Torrente; Federica, Consoli; Rosangela, Ferese; Monia, Magliozzi; Laura, Bernardini; Valentina, Guida; Maria Cristina, Digilio; Marino Taussig De Bodonia, Bruno; Bruno, Dallapiccola; Alessandro De, Luca - 01a Articolo in rivista
rivista: EUROPEAN JOURNAL OF MEDICAL GENETICS (AMSTERDAM, NETHERLANDS,: ELSEVIER SCIENCE BV) pp. 80-87 - issn: 1769-7212 - wos: WOS:000314627900003 (51) - scopus: 2-s2.0-84873188975 (52)
11573/560040 - 2013 -
Atrioventricular canal defect in patients with RASopathies Maria Cristina Digilio, ; Lepri, F. R.; Dentici, M. L.; Francesca Romana Lepri, ; Dentici, M. L.; Maria Lisa Dentici, ; Dentici, Lisa M.; Alex, Henderson; Anwar, Baban; Maria Cristina Roberti, ; Roberti, M. C.; Roberti, Cristina M.; Rossella, Capolino; Versacci, Paolo; Cecilia, Surace; Adriano, Angioni; Marco, Tartaglia; Marino Taussig De Bodonia, Bruno; Dalla Piccola, Bruno; Bruno, Marino; Bruno, Dallapiccola - 01a Articolo in rivista
rivista: EUROPEAN JOURNAL OF HUMAN GENETICS (-NATURE PUBLISHING GROUP, MACMILLAN BUILDING, 4 CRINAN ST, LONDON, ENGLAND, N1 9XW
-S Karger AG:Allschwilerstrasse 10, CH-4009 Basel Switzerland:011 41 61 3061111, EMAIL: orders@karger.ch, INTERNET: http://www.karger.com, Fax: 011 41 61 3061234) pp. 200-204 - issn: 1018-4813 - wos: WOS:000314003300011 (20) - scopus: 2-s2.0-84872498338 (21)
11573/560029 - 2013 -
JAG1 Mutation in a patient with deletion 22q11.2 syndrome and tetralogy of Fallot Maria Cristina, Digilio; Luca, Ad; Alessandro De, Luca; Alessandro De, Luca; Francesca, Lepri; Valentina, Guida; Rosangela, Ferese; Maria Lisa, Dentici; Adriano, Angioni; Marino Taussig De Bodonia, Bruno; Dalla Piccola, Bruno; Bruno, Marino; Bruno, Dallapiccola - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS. PART A (WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030) pp. 3133-3136 - issn: 1552-4833 - wos: WOS:000330038000026 (9) - scopus: 2-s2.0-84888058008 (12)
Putotto, C; Unolt, M; Caiaro, A; Marino Taussig De Bodonia, Bruno; Massaccesi, V; Digilio, Mc - 01g Articolo di rassegna (Review)
rivista: GIORNALE ITALIANO DI CARDIOLOGIA (ROMA: Il Pensiero Scientifico
Roma : C.E.P.I. Centro editoriale pubblicitario italiano) pp. 120-125 - issn: 1972-6481 - wos: (0) - scopus: 2-s2.0-84874778783 (1)
11573/759250 - 2013 -
Double outlet right ventricle versus aortic dextroposition: morphologically distinct defects Restivo, A; Unolt, M; Putotto, C; Marino Taussig De Bodonia, Bruno - 01b Commento, Erratum, Replica e simili
rivista: THE ANATOMICAL RECORD (Hoboken, NJ : John Wiley & Sons, 2007-) pp. 559-563 - issn: 1932-8486 - wos: WOS:000316331300003 (6) - scopus: 2-s2.0-84883178493 (7)
11573/780440 - 2013 -
Leftward Displacement of Septum Primum in Children With Congenital Heart Disease Silvestri, Lucia Martina; Alessia, Scarabotti; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: PEDIATRIC CARDIOLOGY (Springer-Verlag New York Incorporated:175 Fifth Avenue:New York, NY 10010:(212)460-1500, EMAIL: orders@springer-ny.com, INTERNET: http://www.springer-ny.com, Fax: (212)533-3503) pp. 185-185 - issn: 0172-0643 - wos: WOS:000329374800030 (4) - scopus: 2-s2.0-84893069554 (5)
11573/541421 - 2013 -
Transposition of great arteries: new insights into the pathogenesis. Unolt, Marta; Putotto, Carolina; Silvestri, L. M.; Marino, D.; Scarabotti, A.; Massaccesi, Valerio; Caiaro, Angela; Versacci, P.; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: FRONTIERS IN PEDIATRICS (Lausanne : Frontiers Media S.A., 2013-) pp. 11- - issn: 2296-2360 - wos: WOS:000209895600011 (59) - scopus: 2-s2.0-84905174782 (73)
11573/508353 - 2012 -
Spiral shapes in heart and shells: when form and function do matter Amodeo, A.; Oliverio, Marco; Versacci, P.; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: EUROPEAN JOURNAL OF CARDIO-THORACIC SURGERY (Oxford: Oxford University Press on behalf of the European Association for Cardio-Thoracic Surgery
Amsterdam: Elsevier Science
Berlin: Springer, 1987-) pp. 473-475 - issn: 1010-7940 - wos: WOS:000300507400009 (3) - scopus: 2-s2.0-84861419130 (4)
11573/759241 - 2012 -
Atrioventricular canal defect as a sign of laterality defect in Ellis-van Creveld and polydactyly syndromes with ciliary and hedgehog signaling dysfunction Digilio, Mc; Dalla Piccola, Bruno; Marino Taussig De Bodonia, Bruno - 01b Commento, Erratum, Replica e simili
rivista: PEDIATRIC CARDIOLOGY (Springer-Verlag New York Incorporated:175 Fifth Avenue:New York, NY 10010:(212)460-1500, EMAIL: orders@springer-ny.com, INTERNET: http://www.springer-ny.com, Fax: (212)533-3503) pp. 874-875 - issn: 0172-0643 - wos: WOS:000304458900041 (9) - scopus: 2-s2.0-84863989018 (10)
11573/510045 - 2012 -
Blocked atrial bi/trigeminy in utero evolving in supraventricular tachycardia after birth. Martucci, Vanessa; A., Cerekja; Caiaro, Angela; Bosco, Giovanna; Lucchini, Renato; G., Piacentini; Marino Taussig De Bodonia, Bruno; Ventriglia, Flavia - 01a Articolo in rivista
rivista: CASE REPORTS IN OBSTETRICS AND GYNECOLOGY (Cairo: Hindawi Publishing Corporation) pp. 1-3 - issn: 2090-6692 - wos: (0) - scopus: (0)
11573/496492 - 2012 -
Overt cleft palate phenotype and TBX1 genotype correlations in velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patients Sean B., Herman; Tingwei, Guo; D. M. M., Mcginn; Anna, Blonska; Alan L., Shanske; Anne S., Bassett; Eva W. C., Chow; Mark, Bowser; Molly, Sheridan; Frits, Beemer; Koen, Devriendt; Ann, Swillen; Jeroen, Breckpot; M., Cristina Digilio; Marino Taussig De Bodonia, Bruno; Bruno, Dallapiccola; Courtney, Carpenter; Xin, Zheng; Jacob, Johnson; Jonathan, Chung; Anne Marie, Higgins; N., Philip; Tony, Simon; Karlene, Coleman; Damian Heine, Suner; Jordi, Rosell; Wendy, Kates; Devoto, Marcella; Elaine, Zackai; Tao, Wang; Robert, Shprintzen; Beverly S., Emanuel; B. E., Morrow - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS. PART A (WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030) pp. 2781-2787 - issn: 1552-4825 - wos: WOS:000310071700023 (18) - scopus: 2-s2.0-84867839924 (19)
11573/426314 - 2011 -
Clinical, pathological, and molecular analyses of cardiovascular abnormalities in Costello syndrome: a Ras/MAPK pathway syndrome. Angela E., Lin; M. E., Alexander; Steven D., Colan; Bronwyn, Kerr; Katherine A., Rauen; Jacqueline, Noonan; Jeanne, Baffa; Elizabeth, Hopkins; Katia Sol, Church; Giuseppe, Limongelli; Maria Christina, Digilio; Marino Taussig De Bodonia, Bruno; A., Micheil Innes; Yoko, Aoki; Michael, Silberbach; Marie Ange, Delrue; Susan M., White; Robert M., Hamilton; William, O'connor; Paul D., Grossfeld; Leslie B., Smoot; Robert F., Padera; Karen W., Gripp - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS. PART A (WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030) pp. 486-507 - issn: 1552-4825 - wos: WOS:000288033300008 (86) - scopus: 2-s2.0-79952017072 (101)
11573/426309 - 2011 -
Practical Guidelines for Managing Patients with 22q11.2 Deletion Syndrome Anne S., Bassett; Donna M., Mcdonald Mcginn; Koen, Devriendt; Maria Cristina, Digilio; Paula, Goldenberg; Alex, Habel; Marino Taussig De Bodonia, Bruno; Solveig, Oskarsdottir; N., Philip; Kathleen, Sullivan; Ann, Swillen; Jacob, Vorstman; 2., Deletion Syndrome Consortium International 22Q11 - 01a Articolo in rivista
rivista: THE JOURNAL OF PEDIATRICS (New York NY: Elsevier
St. Louis Mo.: C.V. Mosby) pp. 332-U213 - issn: 0022-3476 - wos: WOS:000292878400031 (362) - scopus: 2-s2.0-79960444931 (445)
11573/426315 - 2011 -
Genetic Dosage Compensation in a Family with Velo-Cardio-Facial/DiGeorge/22q11.2 Deletion Syndrome Avishai A., Alkalay; Tingwei, Guo; Cristina, Montagna; M., Cristina Digilio; Dalla Piccola, Bruno; Marino Taussig De Bodonia, Bruno; Bernice, Morrow - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS. PART A (WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030) pp. 548-554 - issn: 1552-4825 - wos: WOS:000288033300014 (7) - scopus: 2-s2.0-79951963982 (8)
11573/114744 - 2011 -
Truncus Arteriosus with Unilateral Absence of the Left Proximal Pulmonary Artery and DiGeorge Syndrome Casinelli, Emanuela; Boccuzzi, Elena; Versacci, P.; Marino Taussig De Bodonia, Bruno - 01b Commento, Erratum, Replica e simili
rivista: JOURNAL OF CARDIAC SURGERY (Mount Kisco, N.Y. : Futura Pub. Co., c1986-) pp. 559-559 - issn: 0886-0440 - wos: WOS:000295266500027 (1) - scopus: 2-s2.0-80053381641 (2)
11573/759236 - 2011 -
New mutations in ZFPM2/FOG2 gene in tetralogy of fallot and double outlet right ventricle De Luca, A; Sarkozy, A; Ferese, R; Consoli, F; Lepri, F; Dentici, Ml; Vergara, P; De Zorzi, A; Versacci, P; Digilio, Mc; Marino Taussig De Bodonia, Bruno; Dalla Piccola, Bruno - 01a Articolo in rivista
rivista: CLINICAL GENETICS (Oxford : Blackwell) pp. 184-190 - issn: 1399-0004 - wos: WOS:000292650800014 (59) - scopus: 2-s2.0-79960209628 (65)
11573/759232 - 2011 -
RASophathies: clinical diagnosis in the first year of life. Digilio, Mc; Lepri, F; Baban, A; Dentici, Ml; Versacci, P; Capolino, R; Ferese, R; De Luca, A; Tartaglia, M; Marino Taussig De Bodonia, Bruno; Dalla Piccola, Bruno - 01a Articolo in rivista
rivista: MOLECULAR SYNDROMOLOGY (Basel : S. Karger AG, 2010-) pp. 282-289 - issn: 1661-8777 - wos: (0) - scopus: 2-s2.0-80053203956 (73)
11573/759240 - 2011 -
Atrioventricular canal defect and associated genetic disorders: new insights into polydactyly syndromes Digilio, Mc; Versacci, P; Lepri, F; Baban, A; Dalla Piccola, Bruno; Marino Taussig De Bodonia, Bruno - 01b Commento, Erratum, Replica e simili
rivista: CARDIOGENETICS (Pavia; PagePress) pp. e7- - issn: 2035-8253 - wos: (0) - scopus: (0)
11573/426313 - 2011 -
SOS1 Mutations in Noonan Syndrome: Molecular Spectrum, Structural Insights on Pathogenic Effects, and Genotype-Phenotype Correlations Francesca, Lepri; Alessandro De, Luca; Lorenzo, Stella; Cesare, Rossi; Giuseppina, Baldassarre; Francesca, Pantaleoni; Viviana, Cordeddu; Bradley J., Williams; Maria L., Dentici; Caputo, Viviana; Serenella, Venanzi; Michela, Bonaguro; Ines, Kavamura; Maria F., Faienza; Alba, Pilotta; Franco, Stanzial; Francesca, Faravelli; Orazio, Gabrielli; Marino Taussig De Bodonia, Bruno; Giovanni, Neri; Margherita Cirillo, Silengo; Giovanni B., Ferrero; Isabella, Torrrente; Angelo, Selicorni; Laura, Mazzanti; Maria C., Digilio; Giuseppe, Zampino; Dalla Piccola, Bruno; Bruce D., Gelb; Marco, Tartaglia - 01a Articolo in rivista
rivista: HUMAN MUTATION (John Wiley & Sons Incorporated:Customer Service, 111 River Street:Hoboken, NJ 07030:(800)225-5945, (201)748-6000, EMAIL: societyinfo@wiley.com, INTERNET: http://www.wiley.com, Fax: (212)748-6551) pp. 760-772 - issn: 1059-7794 - wos: WOS:000292551800009 (93) - scopus: 2-s2.0-79959745810 (99)
11573/759238 - 2011 -
Novel and recurrent JAG1 mutations in patients with tetralogy of fallot Guida, V; Chiappe, F; Ferese, R; Usala, G; Maestrale, G; Iannascoli, C; Bellacchio, E; Mingarelli, R; Digilio, Mc; Marino Taussig De Bodonia, Bruno; Uda, M; De Luca, A; Dalla Piccola, Bruno - 01b Commento, Erratum, Replica e simili
rivista: CLINICAL GENETICS (Oxford : Blackwell) pp. 591-594 - issn: 1399-0004 - wos: WOS:000296915000014 (8) - scopus: 2-s2.0-80054900256 (10)
11573/426312 - 2011 -
Screening for 22q11.2 microdeletion in adults with tetralogy of Fallot M. C., Digilio; Marino Taussig De Bodonia, Bruno; Dalla Piccola, Bruno - 01a Articolo in rivista
rivista: HEART (BMJ / British Medical Journal Publishing Group:PO Box 299, London WC1H 9TD United Kingdom:011 44 20 73836270, EMAIL: subscriptions@bmjgroup.com, INTERNET: http://www.bmjpg.com/bmj, Fax: 011 44 20 73836402) pp. 860-860 - issn: 1355-6037 - wos: WOS:000289789100013 (1) - scopus: 2-s2.0-79955149889 (1)
11573/426307 - 2011 -
Ebstein Anomaly: Genetic Heterogeneity and Association With Microdeletions 1p36 and 8p23.1 Maria Cristina, Digilio; Laura, Bernardini; Francesca, Lepri; Maria Grazia, Giuffrida; Valentina, Guida; Anwar, Baban; Versacci, Paolo; Rossella, Capolino; Barbara, Torres; Alessandro De, Luca; Anna Maria, Novelli; Marino Taussig De Bodonia, Bruno; Dalla Piccola, Bruno - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS. PART A (WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030) pp. 2196-2202 - issn: 1552-4825 - wos: WOS:000294182500024 (31) - scopus: 2-s2.0-84860417458 (35)
11573/495862 - 2011 -
Sindrome di Williams: studio della funzione cardiaca e dell'efficienza cardiorespiratoria Marino Taussig De Bodonia, Bruno; Gallo, Pietro; Macri', Francesco; Musacchio, Angela; Pacella, Elena; Paravati, Vincenzo; Properzi, Enrico; Tancredi, Giancarlo; Ventriglia, Flavia; Nicita, Francesco; Papetti, Laura; Lambiase, Caterina; Versacci, Paolo; A., De Merulis; S., Anaclerio - 13a Altro ministeriale
11573/426316 - 2011 -
Search of somatic GATA4 and NKX2.5 gene mutations in sporadic septal heart defects Marleny, Salazar; Consoli, Federica; Victoria, Villegas; Victor, Caicedo; Valeria, Maddaloni; Paola, Daniele; Giuseppe, Caianiello; Sonia, Pachon; Federico, Nunez; Giuseppe, Limongelli; Giuseppe, Pacileo; Marino Taussig De Bodonia, Bruno; Jaime E., Bernal; Alessandro De, Luca; Dalla Piccola, Bruno - 01a Articolo in rivista
rivista: EUROPEAN JOURNAL OF MEDICAL GENETICS (AMSTERDAM, NETHERLANDS,: ELSEVIER SCIENCE BV) pp. 306-309 - issn: 1769-7212 - wos: WOS:000293744600021 (35) - scopus: 2-s2.0-79955470397 (36)
11573/355792 - 2011 -
Cardiopulmonary response to exercise and cardiac assessment in patients with turner syndrome. Tancredi, Giancarlo; Versacci, Paolo; Anna Maria Pasquino, ; Anna Chiara Vittucci, ; Ida, Pucarelli; Marco, Cappa; Corrado Di Mambro, ; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: THE AMERICAN JOURNAL OF CARDIOLOGY (NY : Elsevier Science Incorporated /
NY; EXCERPTA MEDICA INC) pp. 1076-1082 - issn: 0002-9149 - wos: WOS:000289275500020 (18) - scopus: 2-s2.0-79952745814 (17)
11573/496505 - 2011 -
Genotype and cardiovascular phenotype correlations with TBX1 in 1,022 velo-cardio-facial/digeorge/22q11.2 deletion syndrome patients Tingwei, Guo; Donna Mcdonald, Mcginn; Anna, Blonska; Alan, Shanske; Anne S., Bassett; Eva, Chow; Mark, Bowser; Molly, Sheridan; Frits, Beemer; Koen, Devriendt; Ann, Swillen; Jeroen, Breckpot; Maria C., Digilio; Marino Taussig De Bodonia, Bruno; Dalla Piccola, Bruno; Courtney, Carpenter; Xin, Zheng; Jacob, Johnson; Jonathan, Chung; Philip N., Higgins Am; Tony J., Simon; Karlene, Coleman; Damian Heine, Suner; Jordi, Rosell; Wendy, Kates; Devoto, Marcella; Elizabeth, Goldmuntz; Elaine, Zackai; Tao, Wang; Robert, Shprintzen; Beverly, Emanuel; Bernice, Morrow - 01a Articolo in rivista
rivista: HUMAN MUTATION (John Wiley & Sons Incorporated:Customer Service, 111 River Street:Hoboken, NJ 07030:(800)225-5945, (201)748-6000, EMAIL: societyinfo@wiley.com, INTERNET: http://www.wiley.com, Fax: (212)748-6551) pp. 1278-1289 - issn: 1059-7794 - wos: WOS:000296429800012 (46) - scopus: 2-s2.0-80054695658 (52)
11573/103755 - 2011 -
The heart and shell. Anatomical and genetic similarities Versacci, Paolo; Digilio, Mc; Oliverio, Marco; Dallapiccola, B; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: AMERICAN HEART JOURNAL (St. Louis: Elsevier [etc.]) pp. 647-649 - issn: 0002-8703 - wos: WOS:000289190500005 (5) - scopus: 2-s2.0-79953714866 (5)
11573/426317 - 2011 -
Surgical results in patients with cardiac defects and del 22q11.2 Syndrome Versacci, Paolo; Guido, Michielon; Adriano, Carotti; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: THE AMERICAN JOURNAL OF CARDIOLOGY (NY : Elsevier Science Incorporated /
NY; EXCERPTA MEDICA INC) pp. 337-338 - issn: 0002-9149 - wos: WOS:000286789200034 (1) - scopus: 2-s2.0-78650863657 (1)
11573/366253 - 2010 -
Familial transposition of the great arteries caused by multiple mutations in laterality genes A., De Luca; A., Sarkozy; F., Consoli; R., Ferese; V., Guida; M. L., Dentici; R., Mingarelli; E., Bellacchio; G., Tuo; G., Limongelli; M. C., Digilio; Marino Taussig De Bodonia, Bruno; Dalla Piccola, Bruno - 01a Articolo in rivista
rivista: HEART (BMJ / British Medical Journal Publishing Group:PO Box 299, London WC1H 9TD United Kingdom:011 44 20 73836270, EMAIL: subscriptions@bmjgroup.com, INTERNET: http://www.bmjpg.com/bmj, Fax: 011 44 20 73836402) pp. 673-677 - issn: 1355-6037 - wos: WOS:000277066500009 (93) - scopus: 2-s2.0-77951655078 (107)
11573/114686 - 2010 -
Exclusion of Cx43 gene mutation as a major cause of criss-cross heart anomaly in man Alessandro De, Luca; Anna, Sarkozy; Federica, Consoli; Andrea De, Zorzi; Rita, Mingarelli; Maria Cristina, Digilio; Marino Taussig De Bodonia, Bruno; Bruno, Dallapiccola - 01a Articolo in rivista
rivista: INTERNATIONAL JOURNAL OF CARDIOLOGY (Elsevier Science Ireland Limited:PO Box 85, Limerick Ireland:011 353 61 709600, 011 353 61 61944, EMAIL: usinfo-f@elsevier.com, INTERNET: http://www.elsevier.com, Fax: 011 353 61 709114) pp. 300-302 - issn: 0167-5273 - wos: WOS:000282678300053 (4) - scopus: 2-s2.0-77957840150 (5)
11573/114739 - 2010 -
Isolated Cleft of the Mitral Valve: Its Pathogenic Relationship with Endocardial Cushion Defects Boccuzzi, E.; Casinelli, E.; Versacci, P.; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: TEXAS HEART INSTITUTE JOURNAL (Texas Heart Institute:PO Box 20345, Mail Code 1-194:Houston, TX 77225:(832)355-6630, INTERNET: http://www.texasheartinstitute.org, Fax: (832)355-3714) pp. 503-503 - issn: 0730-2347 - wos: WOS:000280752000030 (2) - scopus: 2-s2.0-77957332450 (2)
11573/112204 - 2010 -
Congenital diaphragmatic hernia after exposure to a triple retinoic acid antagonist during pregnancy Daria, Cipollone; Cozzi, Denis; Businaro, Rita; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: JOURNAL OF CARDIOVASCULAR MEDICINE (Lippincott Williams & Wilkins) pp. - - issn: 1558-2027 - wos: WOS:000401268400017 (3) - scopus: 2-s2.0-78549261467 (4)
11573/1666619 - 2010 -
A rare case of cystic variety of angiomatoid fibrous histiocytoma (European Review for Medical and Pharmacological Sciences (2010) 14, 10 (887-890)) Filingeri, V.; Bellini, I.; Marino, B.; Frantoni, S.; Schiaroli, S. - 01b Commento, Erratum, Replica e simili
rivista: EUROPEAN REVIEW FOR MEDICAL AND PHARMACOLOGICAL SCIENCES (Roma: Verduci publisher.) pp. - - issn: 1128-3602 - wos: (0) - scopus: 2-s2.0-79951815649 (0)
11573/1603404 - 2010 -
A rare case of cystic variety of angiomatoid fibrous histiocytoma Filingeri, V.; Bellini, I.; Marino, B.; Fratoni, S.; Schiaroli, S. - 01b Commento, Erratum, Replica e simili
rivista: EUROPEAN REVIEW FOR MEDICAL AND PHARMACOLOGICAL SCIENCES (Roma: Verduci publisher.) pp. 887-890 - issn: 1128-3602 - wos: WOS:000285641700015 (0) - scopus: 2-s2.0-79951815649 (0)
11573/1666618 - 2010 -
A rare case of cystic variety of angiomatoid fibrous histiocytoma Filingeri, V.; Bellini, I.; Marino, B.; Fratoni, S.; Schiaroli, S. - 01a Articolo in rivista
rivista: EUROPEAN REVIEW FOR MEDICAL AND PHARMACOLOGICAL SCIENCES (Roma: Verduci publisher.) pp. 887-890 - issn: 1128-3602 - wos: WOS:000283750900011 (2) - scopus: 2-s2.0-79952213118 (1)
11573/114738 - 2010 -
Hif1α down-regulation is associated with transposition of great arteries in mice treated with a retinoic acid antagonist Francesca, Amati; Laura, Diano; Luisa, Campagnolo; Lucia, Vecchione; Daria, Cipollone; Susana, Bueno; Gianluca, Prosperini; Alessandro, Desideri; Gregorio, Siracusa; Giovanni, Chillemi; Marino Taussig De Bodonia, Bruno; Giuseppe, Novelli - 01a Articolo in rivista
rivista: BMC GENOMICS (London: BioMed Central, 2000-) pp. 497- - issn: 1471-2164 - wos: WOS:000282791300001 (13) - scopus: 2-s2.0-77956575323 (16)
11573/114740 - 2010 -
Hypoplastic Left Heart Syndrome in Patients With Kabuki Syndrome M., Cristina Digilio; Anwar, Baban; Marino Taussig De Bodonia, Bruno; B., Marino Taussig De Bodonia; Bruno, Dallapiccola - 01b Commento, Erratum, Replica e simili
rivista: PEDIATRIC CARDIOLOGY (Springer-Verlag New York Incorporated:175 Fifth Avenue:New York, NY 10010:(212)460-1500, EMAIL: orders@springer-ny.com, INTERNET: http://www.springer-ny.com, Fax: (212)533-3503) pp. 1111-1113 - issn: 0172-0643 - wos: WOS:000282424800030 (11) - scopus: 2-s2.0-77957578096 (14)
11573/230570 - 2010 -
Shells and heart: Are human laterality and chirality of snails controlled by the same maternal genes? Oliverio, Marco; Digilio, Mc; Versacci, Paolo; Dallapiccola, B; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS. PART A (WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030) pp. 2419-2425 - issn: 1552-4825 - wos: WOS:000283103700001 (31) - scopus: 2-s2.0-78349252289 (32)
Ruggero, D'anastasio; Gianpaolo Di Silvestro, ; Versacci, Paolo; Luigi, Capasso; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: THE LANCET (Lancet Limited:42 Bedford Square, London WC1B 3SL United Kingdom:011 44 207 4364981, EMAIL: custserv@lancet.com, INTERNET: http://www.thelancet.com, Fax: 011 44 207 3236433) pp. 2168-2168 - issn: 0140-6736 - wos: WOS:000279255100027 (8) - scopus: 2-s2.0-77953615956 (12)
11573/114743 - 2010 -
No proof that Santa Rosa heart thrombus was antemortem – Authors' reply Ruggero, D'anastasio; Versacci, Paolo; Luigi, Capasso; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: THE LANCET (Lancet Limited:42 Bedford Square, London WC1B 3SL United Kingdom:011 44 207 4364981, EMAIL: custserv@lancet.com, INTERNET: http://www.thelancet.com, Fax: 011 44 207 3236433) pp. 1052- - issn: 0140-6736 - wos: WOS:000282411600027 (0) - scopus: 2-s2.0-77957204378 (1)
Tarani, Luigi; Maria C., Digilio; Bruno, Dallapiccola; Donna M., Mc Donald Mcginn; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: THE ITALIAN JOURNAL OF PEDIATRICS (London: BioMed Central Ltd. 2008-
-Pacini Editore) pp. 22- - issn: 1720-8424 - wos: WOS:000293228300001 (0) - scopus: (0)
11573/114741 - 2010 -
Multiplex ligation-dependent probe amplification analysis of GATA4 gene copy number variations in patients with isolated congenital heart disease Valentina, Guida; Francesca, Lepri; Raymon, Vijzelaar; Andrea, De Zorzi; Versacci, Paolo; Maria, Cristina Digilio; Marino Taussig De Bodonia, Bruno; Alessandro, De Luca; Bruno, Dallapiccola - 01a Articolo in rivista
rivista: DISEASE MARKERS (Cairo : Hindawi Publishing Corporation
Amsterdam Netherlands: IOS Press) pp. 287-292 - issn: 0278-0240 - wos: WOS:000279321700004 (9) - scopus: 2-s2.0-77954813132 (11)
11573/114480 - 2009 -
New Findings concerning Cardiovascular Manifestations emerging from Long-term Follow-up of 150 patients with the Williams-Beuren-Beuren syndrome Alessia Del, Pasqua; Gabriele, Rinelli; Alessandra, Toscano; Roberta, Iacobelli; Cristina, Digilio; Marino Taussig De Bodonia, Bruno; Claudia, Saffirio; Sergio, Mondillo; Luciano, Pasquini; Stephen Pruett, Sanders; A., De Zorzi - 01a Articolo in rivista
rivista: CARDIOLOGY IN THE YOUNG (Greenwich Medical Media Limited:137 Euston Road, London NW1 2AA United Kingdom:011 44 20 73885444, INTERNET: http://www.greenwich-medical.co.uk, Fax: 011 44 20 86695891) pp. 563-567 - issn: 1047-9511 - wos: WOS:000282858600003 (44) - scopus: 2-s2.0-76349112682 (47)
11573/112155 - 2009 -
Germline BRAF mutations in noonan, LEOPARD, and cardiofaciocutaneous Syndromes: Molecular diversity and associated phenotypic spectrum Anna, Sarkozy; Claudio, Carta; Sonia, Moretti; Giuseppe, Zampino; Maria C., Digilio; Francesca, Pantaleoni; Anna Paola, Scioletti; Giorgia, Esposito; Viviana, Cordeddu; Francesca, Lepri; Valentina, Petrangeli; Maria L., Dentici; Grazia M. S., Mancini; Angelo, Selicorni; Cesare, Rossi; Laura, Mazzanti; Marino Taussig De Bodonia, Bruno; Giovanni B., Ferrero; Margherita Cirillo, Silengo; Luigi, Memo; Franco, Stanzial; Francesca, Faravelli; Liborio, Stuppia; Efisio, Puxeddu; Bruce D., Gelb; Bruno, Dallapiccola; Marco, Tartaglia - 01a Articolo in rivista
rivista: HUMAN MUTATION (John Wiley & Sons Incorporated:Customer Service, 111 River Street:Hoboken, NJ 07030:(800)225-5945, (201)748-6000, EMAIL: societyinfo@wiley.com, INTERNET: http://www.wiley.com, Fax: (212)748-6551) pp. 695-702 - issn: 1059-7794 - wos: WOS:000265006400025 (204) - scopus: 2-s2.0-63749111765 (220)
11573/228398 - 2009 -
Folic acid and methionine in the prevention of teratogen-induced congenital defects in mice Daria, Cipollone; Rita, Carsetti; Angela, Tagliani; Maria Manuela, Rosado; Paola, Borgiani; Giuseppe, Novelli; D'amati, Giulia; Fumagalli, Lorenzo; Marino Taussig De Bodonia, Bruno; Businaro, Rita - 01a Articolo in rivista
rivista: CARDIOVASCULAR PATHOLOGY (Elsevier Science Incorporated / NY Journals:Madison Square Station, PO Box 882:New York, NY 10159:(212)633-3730, EMAIL: usinfo-f@elsevier.com, INTERNET: http://www.elsevier.com, Fax: (212)633-3680) pp. 100-109 - issn: 1054-8807 - wos: WOS:000264403200005 (17) - scopus: 2-s2.0-61349100859 (15)
libro: XXXVII Congresso Nazionale Società Italiana di Cardiologia Pediatrica, (SICP 2008) - ()
11573/230040 - 2009 -
Molecular Analysis of PRKAG2, LAMP2, and NKX2-5 Genes in a Cohort of 125 Patients With Accessory Atrioventricular Connection Giorgia, Esposito; Giorgia, Grutter; Fabrizio, Drago; Mauro W., Costa; Antonella De, Santis; Bosco, Giovanna; Marino Taussig De Bodonia, Bruno; Emanuele, Bellacchio; Francesca, Lepri; Richard P., Harvey; Anna, Sarkozy; Bruno, Dallapiccola - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS. PART A (WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030) pp. 1574-1577 - issn: 1552-4825 - wos: WOS:000267770000036 (17) - scopus: 2-s2.0-67649889416 (18)
11573/114687 - 2009 -
Impact of DEL22q11, trisomy 21, and other genetic syndromes on surgical outcome of conotruncal heart defects Guido, Michielon; Marino Taussig De Bodonia, Bruno; Gianluca, Oricchio; Maria Cristina, Digilio; Fiore, Iorio; Sergio, Filippelli; Silvia, Placidi; Roberto M., Di Donato - 01a Articolo in rivista
rivista: JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY (New York: Elsevier
Orlando, FL: Mosby Year Book) pp. 565-570.e2 - issn: 0022-5223 - wos: WOS:000269323000007 (50) - scopus: 2-s2.0-68749084593 (59)
11573/114685 - 2009 -
Three patients with oculo-auriculo-vertebral spectrum and microdeletion 22q11.2 M., Cristina Digilio; Donna M., Mcdonald Mcginn; Carrie, Heike; Charles, Catania; Bruno, Dallapiccola; Marino Taussig De Bodonia, Bruno; Elaine H., Zackai - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS. PART A (WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030) pp. 2860-2864 - issn: 1552-4825 - wos: WOS:000272535000037 (53) - scopus: 2-s2.0-71949088054 (54)
11573/114735 - 2009 -
16p subtelomeric duplication: a clinically recognizable syndrome Maria Cristina, Digilio; Laura, Bernardini; Anna, Capalbo; Rossella, Capolino; Maria Giulia, Gagliardi; Marino Taussig De Bodonia, Bruno; Antonio, Novelli; Bruno, Dallapiccola - 01a Articolo in rivista
rivista: EUROPEAN JOURNAL OF HUMAN GENETICS (-NATURE PUBLISHING GROUP, MACMILLAN BUILDING, 4 CRINAN ST, LONDON, ENGLAND, N1 9XW
-S Karger AG:Allschwilerstrasse 10, CH-4009 Basel Switzerland:011 41 61 3061111, EMAIL: orders@karger.ch, INTERNET: http://www.karger.com, Fax: 011 41 61 3061234) pp. 1135-1140 - issn: 1018-4813 - wos: WOS:000269449900007 (20) - scopus: 2-s2.0-69249222747 (20)
11573/112156 - 2009 -
Genetic syndromes and congenital heart defects: how is surgical management affected? Roberto, Formigari; Guido, Michielon; Maria Cristina, Digilio; Gerardo, Piacentini; Adriano, Carotti; Alessandro, Giardini; Roberto M., Di Donato; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: EUROPEAN JOURNAL OF CARDIO-THORACIC SURGERY (Oxford: Oxford University Press on behalf of the European Association for Cardio-Thoracic Surgery
Amsterdam: Elsevier Science
Berlin: Springer, 1987-) pp. 606-614 - issn: 1010-7940 - wos: WOS:000265573300010 (78) - scopus: 2-s2.0-62149141331 (86)
11573/112157 - 2008 -
Cardiac defects and results of cardiac surgery in 22q11.2 deletion syndrome Adriano, Carotti; Maria Cristina, Digilio; Gerardo, Piacentini; Claudia, Saffirio; Roberto M., Di Donato; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS (Hoboken, NJ : Wiley-Blackwell) pp. 35-42 - issn: 1940-5510 - wos: WOS:000259838500006 (84) - scopus: 2-s2.0-44149094257 (103)
11573/114477 - 2008 -
Ductal origin of the distal pulmonary artery in truncus arteriosus. Carotti, A; Piacentini, G; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: ANNALS OF THORACIC SURGERY ([Boston etc.]: [Little Brown & Co. etc.]) pp. 2262-2263 - issn: 0003-4975 - wos: WOS:000246791200076 (1) - scopus: 2-s2.0-34249083135 (1)
11573/112107 - 2008 -
Better surgical prognosis for patients with Down Syndrome Claudia, Saffirio; Marino Taussig De Bodonia, Bruno; Roberto, Formigari - 01a Articolo in rivista
rivista: JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY (New York: Elsevier
Orlando, FL: Mosby Year Book) pp. 230-230 - issn: 0022-5223 - wos: WOS:000252139600048 (8) - scopus: 2-s2.0-37549049327 (8)
11573/229757 - 2008 -
Congenital heart defects in patients with oculo-auriculo-vertebral spectrum (Goldenhar syndrome) Digilio, Mc; Calzolari, F; Capolino, R; Toscano, A; Sarkozy, A; De Zorzi, A; Dalla Piccola, Bruno; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS. PART A (WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030) pp. 1815-1819 - issn: 1552-4825 - wos: WOS:000257785700007 (38) - scopus: 2-s2.0-48949118168 (52)
11573/112105 - 2008 -
Severe, obstructive biventricular hypertrophy in a patient with Costello syndrome: Clinical impact and management Giuseppe, Limongelli; Giuseppe, Pacileo; Maria Cristina, Digilio; Paolo, Calabro'; Giovanni Di, Salvo; Alessandra, Rea; Tiziana, Miele; Alessandro, Frigiola; Anna, Sarkozy; Bruno, Dallapiccola; Marino Taussig De Bodonia, Bruno; Raffaele, Calabro' - 01a Articolo in rivista
rivista: INTERNATIONAL JOURNAL OF CARDIOLOGY (Elsevier Science Ireland Limited:PO Box 85, Limerick Ireland:011 353 61 709600, 011 353 61 61944, EMAIL: usinfo-f@elsevier.com, INTERNET: http://www.elsevier.com, Fax: 011 353 61 709114) pp. e108-e110 - issn: 0167-5273 - wos: WOS:000260903800044 (10) - scopus: 2-s2.0-55549094464 (8)
11573/112108 - 2008 -
Genotype-phenotype analysis and natural history of left ventricular hypertrophy in LEOPARD syndrome. Limongelli, G; Sarkozy, A; Pacileo, G; Calabrò, P; Digilio, Mc; Maddaloni, V; Gagliardi, G; Di Salvo, G; Iacomino, M; Marino Taussig De Bodonia, Bruno; Dallapiccola, B; Calabrò, R. - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS. PART A (WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030) pp. 620-628 - issn: 1552-4825 - wos: WOS:000253650200011 (43) - scopus: 2-s2.0-43049101740 (47)
11573/228052 - 2008 -
Autosomal dominant inheritance of aplasia cutis congenita and congenital heart defect: A possible link to the Adams-Oliver syndrome M. C., Digilio; Marino Taussig De Bodonia, Bruno; Dalla Piccola, Bruno - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS. PART A (WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030) pp. 2842-2844 - issn: 1552-4825 - wos: WOS:000260985400024 (10) - scopus: 2-s2.0-55849129615 (10)
11573/226602 - 2008 -
Costello syndrome: clinical diagnosis in the first year of life M., Cristina Digilio; Anna, Sarkozy; Rossella, Capolino; M., Beatrice Chiarini Testa; Giorgia, Esposito; A., De Zorzi; Renato, Cutrera; Marino Taussig De Bodonia, Bruno; Dalla Piccola, Bruno - 01a Articolo in rivista
rivista: EUROPEAN JOURNAL OF PEDIATRICS (Springer Verlag Germany:Tiergartenstrasse 17, D 69121 Heidelberg Germany:011 49 6221 3450, EMAIL: g.braun@springer.de, INTERNET: http://www.springer.de, Fax: 011 49 6221 345229) pp. 621-628 - issn: 0340-6199 - wos: WOS:000254804400003 (30) - scopus: 2-s2.0-41849141539 (38)
11573/229434 - 2008 -
Deletion 22q11 and isolated congenital heart disease M., Cristina Digilio; Marino Taussig De Bodonia, Bruno; Dalla Piccola, Bruno - 01a Articolo in rivista
rivista: INTERNATIONAL JOURNAL OF CARDIOLOGY (Elsevier Science Ireland Limited:PO Box 85, Limerick Ireland:011 353 61 709600, 011 353 61 61944, EMAIL: usinfo-f@elsevier.com, INTERNET: http://www.elsevier.com, Fax: 011 353 61 709114) pp. 364-365 - issn: 0167-5273 - wos: WOS:000252155000032 (3) - scopus: 2-s2.0-37349109661 (5)
11573/234734 - 2007 -
Hypertrophic cardiomyopathy in a patient with Down's syndrome. Assenza, Ge; Autore, Camillo; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: JOURNAL OF CARDIOVASCULAR MEDICINE (Lippincott Williams & Wilkins) pp. 463-464 - issn: 1558-2027 - wos: WOS:000247986000013 (10) - scopus: 2-s2.0-34248582923 (11)
11573/234364 - 2007 -
Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy Bhaswati, Pandit; Anna, Sarkozy; Len A., Pennacchio; Claudio, Carta; Kimihiko, Oishi; Simone, Martinelli; Edgar A., Pogna; Wendy, Schackwitz; Anna, Ustaszewska; Andrew, Landstrom; J., Martijn Bos; Steve R., Ommen; Giorgia, Esposito; Francesca, Lepri; Christian, Faul; Peter, Mundel; Juan P., Lopez Siguero; Romano, Tenconi; Angelo, Selicorni; Cesare, Rossi; Laura, Mazzanti; Isabella, Torrente; Marino Taussig De Bodonia, Bruno; Maria C., Digilio; Giuseppe, Zampino; Michael J., Ackerman; Dalla Piccola, Bruno; Marco, Tartaglia; Bruce D., Gelb - 01a Articolo in rivista
rivista: NATURE GENETICS (Nature America Incorporated:345 Park Avenue South, 6th Floor:New York, NY 10010:(888)331-6288, EMAIL: institutions@natureny.com, INTERNET: http://www.nature.com, Fax: (212)689-9108) pp. 1007-1012 - issn: 1061-4036 - wos: WOS:000248446900019 (496) - scopus: 2-s2.0-34547530823 (570)
11573/112047 - 2007 -
Familial recurrence of congenital heart disease: an overview and review of the literature. Calcagni, G; Digilio, Mc; Sarkozy, A; Dallapiccola, B; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: EUROPEAN JOURNAL OF PEDIATRICS (Springer Verlag Germany:Tiergartenstrasse 17, D 69121 Heidelberg Germany:011 49 6221 3450, EMAIL: g.braun@springer.de, INTERNET: http://www.springer.de, Fax: 011 49 6221 345229) pp. 111-116 - issn: 0340-6199 - wos: WOS:000243034500002 (54) - scopus: 2-s2.0-33845913514 (67)
11573/112106 - 2007 -
GATA4 as Candidate Gene for Pericardial Defects Claudia, Saffirio; Marino Taussig De Bodonia, Bruno; Maria Cristina, Digilio - 01a Articolo in rivista
rivista: ANNALS OF THORACIC SURGERY ([Boston etc.]: [Little Brown & Co. etc.]) pp. 2137-2137 - issn: 0003-4975 - wos: WOS:000251176300067 (4) - scopus: 2-s2.0-36248990859 (4)
11573/206950 - 2007 -
FOLIC ACID AND METHIONINE IN THE PREVENTION OF TERATOGEN -INDUCED CONGENITAL DEFECTS IN MICE D., Cipollone; A., Tagliani; R., Carsetti; M., Rosado; P., Borgiani; G., Novelli; Marino Taussig De Bodonia, Bruno; Fumagalli, Lorenzo; Businaro, Rita - 04a Atto di comunicazione a congresso
rivista: ITALIAN JOURNAL OF ANATOMY AND EMBRYOLOGY (Mozzon Giuntina SPA:Via Mannelli 29R, I 50136 Florence Italy:011 39 55 2476781, EMAIL: sedicesimo@fol.it, Fax: 011 39 55 2349067
Firenze: Editrice Il Sedicesimo.) pp. 78-78 - issn: 1122-6714 - wos: (0) - scopus: (0)
congresso: 61 congresso società italiana anatomia e istologia (SASSARI)
11573/232072 - 2007 -
Genetics of congenital heart diseases in syndromic and non-syndromic patients: new advances and clinical implications Gerardo, Piacentini; M., Cristina Digilio; Anna, Sarkozy; Silvia, Placidi; Dalla Piccola, Bruno; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: JOURNAL OF CARDIOVASCULAR MEDICINE (Lippincott Williams & Wilkins) pp. 7-11 - issn: 1558-2027 - wos: WOS:000244784400003 (8) - scopus: 2-s2.0-33846611949 (9)
11573/112052 - 2007 -
Familial recurrence of discrete membranous subaortic stenosis Gerardo, Piacentini; Marino Taussig De Bodonia, Bruno; Maria Cristina, Digilio - 01a Articolo in rivista
rivista: JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY (New York: Elsevier
Orlando, FL: Mosby Year Book) pp. 818-819 - issn: 0022-5223 - wos: WOS:000249013300057 (9) - scopus: 2-s2.0-34548130785 (10)
11573/111946 - 2007 -
Univentricular heart and supravalvular ring Gerardo, Piacentini; Silvia, Placidi; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: THE INTERNATIONAL JOURNAL OF CARDIOVASCULAR IMAGING (London; Dordrecht; Boston: Springer
London; Dordrecht; Boston: Kluwer Academic Publishers
Oaklyn, NJ : Field & Wood Publishers) pp. 37-37 - issn: 1569-5794 - wos: WOS:000243821500006 (0) - scopus: 2-s2.0-33846684079 (0)
11573/112051 - 2007 -
Prevalence and. clinical significance of cardiovascular abnormalities in patients with the LEOPARD syndrome Giuseppe, Limongelli; Giuseppe, Pacileo; Marino Taussig De Bodonia, Bruno; Maria Cristina, Digilio; Anna, Sarkozy; Perry, Elliott; Paolo, Versacci; Paolo, Calabro; Andrea De, Zorzi; Giovanni Di, Salvo; Petros, Syrris; Michael, Patton; William J., Mckenna; Bruno, Dallapiccola; Raffaele, Calabro - 01a Articolo in rivista
rivista: THE AMERICAN JOURNAL OF CARDIOLOGY (NY : Elsevier Science Incorporated /
NY; EXCERPTA MEDICA INC) pp. 736-741 - issn: 0002-9149 - wos: WOS:000248873200034 (95) - scopus: 2-s2.0-34547651205 (119)
11573/112152 - 2007 -
Re: Atrioventricular septal defect with common atrioventricular junction, common arterial trunk and severe coartation of the aorta in a patient with Down's syndrome. Saffirio, C; Vittucci, Ac; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: CARDIOLOGY IN THE YOUNG (Greenwich Medical Media Limited:137 Euston Road, London NW1 2AA United Kingdom:011 44 20 73885444, INTERNET: http://www.greenwich-medical.co.uk, Fax: 011 44 20 86695891) pp. 694-694 - issn: 1047-9511 - wos: WOS:000251909900023 (0) - scopus: 2-s2.0-36348958369 (0)
11573/237532 - 2006 -
22q11 Deletion syndrome: a review of some developmental biology aspects of the cardiovascular system Angelo, Restivo; Anna, Sarkozy; Maria Cristina, Digilio; Dalla Piccola, Bruno; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: JOURNAL OF CARDIOVASCULAR MEDICINE (Lippincott Williams & Wilkins) pp. 77-85 - issn: 1558-2027 - wos: WOS:000207498800001 (4) - scopus: 2-s2.0-33646825020 (5)
11573/112043 - 2006 -
Cardiac outflow tract: A review of some embryogenetic aspects of the conotruncal region of the heart Angelo, Restivo; Gerardo, Piacentini; Silvia, Placidi; Claudia, Saffirio; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: ANATOMICAL RECORD. PART A, DISCOVERIES IN MOLECULAR, CELLULAR, AND EVOLUTIONARY BIOLOGY (WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030) pp. 936-943 - issn: 1552-4884 - wos: WOS:000240295400002 (63) - scopus: 2-s2.0-33748112969 (85)
11573/238780 - 2006 -
A multiple retinoic acid antagonist induces conotruncal anomalies, including transposition of the great arteries in mice Daria, Cipollone; Francesca, Amati; Rita, Carsetti; Silvia, Placidi; Michela, Biancolella; D'amati, Giulia; Giuseppe, Novelli; Gregorio, Siracusa; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: CARDIOVASCULAR PATHOLOGY (Elsevier Science Incorporated / NY Journals:Madison Square Station, PO Box 882:New York, NY 10159:(212)633-3730, EMAIL: usinfo-f@elsevier.com, INTERNET: http://www.elsevier.com, Fax: (212)633-3680) pp. 194-202 - issn: 1054-8807 - wos: WOS:000239447800003 (24) - scopus: 2-s2.0-33745871245 (28)
11573/358551 - 2006 -
Feasibility and clinical impact of live three-dimensional echocardiography in the management of congenital heart disease De Castro, Stefano; Caselli, Stefano; Papetti, Federica; Ventriglia, Flavia; Arianna, Giardina; Cavarretta, Elena; Emanuele Di, Angelantonio; Andrea, Marcantonio; Florinda D., Igual Perez; Natesa G., Pandian; Marino Taussig De Bodonia, Bruno; Fedele, Francesco - 01a Articolo in rivista
rivista: ECHOCARDIOGRAPHY (Blackwell Publishing Limited:9600 Garsington Road, Oxford OX4 2DQ United Kingdom:011 44 1865 776868 , (781)388-8200, EMAIL: agentservices@oxon.blackwellpublishing.com, e-help@blackwellpublishers.co.uk, INTERNET: http://www.blackwellpublishing.com, Fax: 011 44 1865 714591) pp. 553-561 - issn: 0742-2822 - wos: WOS:000239332900005 (17) - scopus: 2-s2.0-33746499061 (26)
11573/232911 - 2006 -
LEOPARD syndrome: clinical diagnosis in the first year of life. Digilio, M. C.; Sarkozy, A; De Zorzi, A; Pacileo, G; Limongelli, G; Mingarelli, R; Calabro, R; Marino Taussig De Bodonia, Bruno; Dalla Piccola, Bruno - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS. PART A (WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030) pp. 740-746 - issn: 1552-4825 - wos: WOS:000236679200012 (89) - scopus: 2-s2.0-33646901973 (121)
11573/112046 - 2006 -
Atrioventricular canal defect in Bardet-Biedl syndrome: clinical evidence supporting the link between atrioventricular canal defect and polydactyly syndromes with ciliary dysfunction536. Digilio, Mc; Dallapiccola, B; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: GENETICS IN MEDICINE (New York: Elsevier
Baltimore MD: Williams & Wilkins) pp. 536-538 - issn: 1098-3600 - wos: WOS:000239971600009 (12) - scopus: 2-s2.0-33747220048 (12)
11573/237535 - 2006 -
PTPN11 gene mutations: linking the Gln510Glu mutation to the "LEOPARD syndrome phenotype" Digilio, Mc; Sarkozy, A; Pacileo, G; Limongelli, G; Marino Taussig De Bodonia, Bruno; Dalla Piccola, Bruno - 01a Articolo in rivista
rivista: EUROPEAN JOURNAL OF PEDIATRICS (Springer Verlag Germany:Tiergartenstrasse 17, D 69121 Heidelberg Germany:011 49 6221 3450, EMAIL: g.braun@springer.de, INTERNET: http://www.springer.de, Fax: 011 49 6221 345229) pp. 803-805 - issn: 0340-6199 - wos: WOS:000240717600011 (25) - scopus: 2-s2.0-33748964318 (33)
11573/112049 - 2006 -
Persistent left superior vena cava into unroofed coronary sinus Gerardo, Piacentini; Claudia, Saffirio; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: THE LANCET (Lancet Limited:42 Bedford Square, London WC1B 3SL United Kingdom:011 44 207 4364981, EMAIL: custserv@lancet.com, INTERNET: http://www.thelancet.com, Fax: 011 44 207 3236433) pp. 1963-1964 - issn: 0140-6736 - wos: WOS:000242593300024 (2) - scopus: 2-s2.0-33751395435 (3)
11573/112044 - 2006 -
Diffuse coronary dilation in a young patient with LEOPARD syndrome Giuseppe, Pacileo; Paolo, Calabro; Giuseppe, Limongelli; Giuseppe, Santoro; Mariacristina, Digilio; Anna, Sarkozy; Marino Taussig De Bodonia, Bruno; Bruno, Dallapiccola; Raffaele, Calabro - 01a Articolo in rivista
rivista: INTERNATIONAL JOURNAL OF CARDIOLOGY (Elsevier Science Ireland Limited:PO Box 85, Limerick Ireland:011 353 61 709600, 011 353 61 61944, EMAIL: usinfo-f@elsevier.com, INTERNET: http://www.elsevier.com, Fax: 011 353 61 709114) pp. E35-E37 - issn: 0167-5273 - wos: (0) - scopus: 2-s2.0-33748475818 (11)
11573/111893 - 2006 -
Genetic syndromes and outcome after surgical correction of tetralogy of Fallot Guido, Michielon; Marino Taussig De Bodonia, Bruno; Roberto, Formigari; Gaetano, Gargiulo; Fernando, Picchio; Maria C., Digilio; S., Oricchio Anaclerio; Stephen P., Sanders; Roberto M., Di Donato - 01a Articolo in rivista
rivista: ANNALS OF THORACIC SURGERY ([Boston etc.]: [Little Brown & Co. etc.]) pp. 968-975 - issn: 0003-4975 - wos: WOS:000235844100028 (88) - scopus: 2-s2.0-32644487801 (99)
11573/238427 - 2006 -
Genetic heterogeneity and phenotypic anomalies in children with atrioventricular canal defect and tetralogy of Fallot Pasquale, Vergara; Maria Cristina, Digilio; Andrea De, Zorzi; Carlo, Dd; Rossella, Capolino; Alessandro, Rimini; Monica, Pelegrini; R., Calabro; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: CLINICAL DYSMORPHOLOGY (Lippincott, Williams & Wilkins:530 Walnut Street:Philadelphia, PA 19106:(800)638-3030, (301)223-2300, EMAIL: orders@lww.com, INTERNET: http://www.lww.com, Fax: (301)223-2320, (301)223-2320) pp. 65-70 - issn: 0962-8827 - wos: WOS:000252154700003 (15) - scopus: 2-s2.0-33749235671 (20)
11573/112048 - 2006 -
Re: right isomerism, pulmonary atresia, and major aorto-pulmonary collateral arteries. Piacentini, G; Placidi, S; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: CARDIOLOGY IN THE YOUNG (Greenwich Medical Media Limited:137 Euston Road, London NW1 2AA United Kingdom:011 44 20 73885444, INTERNET: http://www.greenwich-medical.co.uk, Fax: 011 44 20 86695891) pp. 608-609 - issn: 1047-9511 - wos: WOS:000246879900018 (0) - scopus: 2-s2.0-33751229902 (0)
11573/239808 - 2006 -
Types of cardiac defects in children with Down's syndrome. Placidi, S; Digilio, Mc; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: CARDIOLOGY IN THE YOUNG (Greenwich Medical Media Limited:137 Euston Road, London NW1 2AA United Kingdom:011 44 20 73885444, INTERNET: http://www.greenwich-medical.co.uk, Fax: 011 44 20 86695891) pp. 198-199 - issn: 1047-9511 - wos: WOS:000237885100022 (4) - scopus: 2-s2.0-33747739135 (5)
11573/115674 - 2006 -
Additional evidence that PTPN11 mutations play only a minor role in the pathogenesis of non-syndromic atrioventricular canal defect Sarkozy, A; Lepri, F; Marino Taussig De Bodonia, Bruno; Pizzuti, Antonio; Digilio, Mc; Dalla Piccola, Bruno - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS. PART A (WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030) pp. 1970-1972 - issn: 1552-4825 - wos: WOS:000240391800014 (5) - scopus: 2-s2.0-33748597974 (4)
11573/111894 - 2006 -
Familial recurrence of anomalous origin of right pulmonary artery from the aorta Vergara, P; Digilio, Mc; Limongelli, G; Carotti, A; Toscano, A; Santoro, G; Calabro, R; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: ARCHIVES OF PEDIATRICS & ADOLESCENT MEDICINE (American Medical Association:515 North State Street:Chicago, IL 60610:(800)262-2350, (312)464-2518, EMAIL: ama-subs@ama-assn.org, INTERNET: http://www.ama-assn.org, Fax: (312)464-5600) pp. 794-796 - issn: 1072-4710 - wos: WOS:000236679200022 (0) - scopus: 2-s2.0-33646936139 (0)
11573/237849 - 2005 -
Spectrum of atrial septal defects associated with mutations of NKX2.5 and GATA4 transcription factors A., Sarkozy; E., Conti; C., Neri; R., D'agostino; M. C., Digilio; G., Esposito; A., Toscano; Marino Taussig De Bodonia, Bruno; Pizzuti, Antonio; Dalla Piccola, Bruno - 01a Articolo in rivista
rivista: JOURNAL OF MEDICAL GENETICS (BMJ / British Medical Journal Publishing Group:PO Box 299, London WC1H 9TD United Kingdom:011 44 20 73836270, EMAIL: subscriptions@bmjgroup.com, INTERNET: http://www.bmjpg.com/bmj, Fax: 011 44 20 73836402) pp. e16-e16 - issn: 0022-2593 - wos: WOS:000226748100026 (127) - scopus: 2-s2.0-28444447608 (134)
11573/362378 - 2005 -
NF1 gene mutations represent the major molecular event underlying neurofibromatosis-Noonan syndrome De Luca, A.; Bottillo, I.; Sarkozy, C.; Carta, C.; Neri, C.; Bellacchio, E.; Schirinzi, A.; Conti, E.; Zampino, G.; Battaglia, A.; Majore, S.; Rinaldi, M. M.; Carella, M.; Marino Taussig De Bodonia, Bruno; Pizzuti, Antonio; Digilio, M. C.; Tartaglia, M.; Dalla Piccola, Bruno - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF HUMAN GENETICS (University of Chicago Press:PO Box 37005, Journals Division:Chicago, IL 60637:(877)705-1878, (877)705-1878, (773)753-2247, EMAIL: subscriptions@press.uchicago.edu, INTERNET: http://www.press.uchicago.edu, Fax: (877)705-1879, (773)753-0811) pp. 1092-1101 - issn: 0002-9297 - wos: WOS:000233241200017 (111) - scopus: 2-s2.0-28144437387 (124)
11573/111602 - 2005 -
Congenital intrahepatic portosystemic venous shunt: an unusual feature in
LEOPARD syndrome and in neurofibromatosis type 1. Digilio M., C; Capolino, R; Marino Taussig De Bodonia, Bruno; Sarkozy, A; Dallapiccola, B. - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS. PART A (WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030) pp. 457-458 - issn: 1552-4825 - wos: WOS:000228758400022 (5) - scopus: 2-s2.0-18044380133 (8)
11573/111606 - 2005 -
Familial recurrence of heart defects in subjects with congenitally corrected transposition of the great arteries Gerardo, Piacentini; M., Cristina Digilio; Rossella, Capolino; Andrea De, Zorzi; Alessandra, Toscano; Anna, Sarkozy; Rita, D'agostino; Maurizio, Marasini; M., Giovanna Russo; Bruno, Dallapiccola; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS. PART A (WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030) pp. 176-180 - issn: 1552-4825 - wos: WOS:000231634600010 (18) - scopus: 2-s2.0-24344440728 (31)
11573/111603 - 2005 -
Familial recurrence of nonsyndromic congenital heart defects in first degree relatives of patients with deletion 22q11.2 M., Cristina Digilio; Marino Taussig De Bodonia, Bruno; Rossella, Capolino; Adriano, Angioni; Anna, Sarkozy; M., Cristina Roberti; Emanuela, Conti; A., De Zorzi; Bruno, Dallapiccola - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS. PART A (WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030) pp. 158-164 - issn: 1552-4825 - wos: WOS:000228037500006 (13) - scopus: 2-s2.0-15944413776 (12)
11573/111605 - 2005 -
Association of deletion 22 and trisomy 21: A likely random association in patients with conotruncal heart defects Maria Cristina, Digilio; Bruno, Dallapiccola; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS. PART A (WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030) pp. 1-2 - issn: 1552-4825 - wos: WOS:000227966700001 (5) - scopus: 2-s2.0-15744401912 (4)
11573/237017 - 2005 -
CRELD1 and GATA4 gene analysis in patients with nonsyndromic atrioventricular canal defects. Sarkozy, A.; Esposito, G.; Conti, E.; Digilio, M. C.; Marino Taussig De Bodonia, Bruno; Calabro, R.; Pizzuti, Antonio; Dallapiccola, B. - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS. PART A (WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030) pp. 236-238 - issn: 1552-4825 - wos: WOS:000233756600012 (21) - scopus: 2-s2.0-28444474221 (22)
11573/240789 - 2005 -
ZEPM2/FOG2 AND HEY2 GENES ANALYSIS IN NONSYNDROMIC TRICUSPID ATRESIA Sarkozy, A; Conti, E; D'agostino, R; Digilio M., C; Formigari, R; Picchio, F; Marino Taussig De Bodonia, Bruno; Pizzuti, Antonio; Dalla Piccola, Bruno - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS. PART A (WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030) pp. 68-70 - issn: 1552-4825 - wos: WOS:000226619200013 (11) - scopus: 2-s2.0-12944255784 (15)
11573/111607 - 2005 -
Absent pulmonary valve with intact ventricular septum and patent ductus arteriosus: a specific cardiac phenotype associated with deletion 18q syndrome Versacci, P; Digilio M., C; Sauer, U; Dalla Piccola, B; Marino Taussig De Bodonia, B. - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS. PART A (WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030) pp. 185-186 - issn: 1552-4825 - wos: WOS:000232239200019 (18) - scopus: 2-s2.0-25644446922 (23)
11573/233652 - 2004 -
Clinical and molecular analysis of 30 patients with multiple lentigines LEOPARD syndrome A., Sarkozy; E., Conti; M. C., Digilio; Marino Taussig De Bodonia, Bruno; E., Morini; G., Pacileo; M., Wilson; R., Calabro'; Pizzuti, Antonio; Dalla Piccola, Bruno - 01a Articolo in rivista
rivista: EJMG (London: BMJ Publishing Group.) pp. e68-e68 - issn: 1468-6244 - wos: WOS:000221165600028 (101) - scopus: 2-s2.0-3042761427 (125)
11573/112803 - 2004 -
Conotruncal heart defects: impact of genetic syndromes on immediate operative mortality. Anaclerio, S.; Di Ciommo, V.; Michielon, G.; Digilio, M. C.; Formigari, R.; Picchio, F. M.; Gargiulo, G.; Di Donato, R.; De Ioris, M. A.; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: ITALIAN HEART JOURNAL (Roma : C.E.P.I. Centro editoriale pubblicitario italiano) pp. 624-628 - issn: 1129-471X - wos: (0) - scopus: 2-s2.0-16644383757 (69)
11573/238354 - 2004 -
Influence of heart rate on left ventricular isovolumic relaxation time: a Doppler study in healthy newborns Antonio De, Merulis; Giulio, Calcagni; Paolo, Versacci; Lucchini, Renato; Flavia, Ventriglia; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: JOURNAL OF THE AMERICAN SOCIETY OF ECHOCARDIOGRAPHY (Mosby Year Book Incorporated:6277 Sea Harbor Drive:Orlando, FL 32887:(800)654-2452, (407)345-4000, EMAIL: hhspcs@harcourt.com, INTERNET: http://www.mosby.com, Fax: (407)363-9661, (314)432-1380) pp. 330-331 - issn: 0894-7317 - wos: WOS:000220651100006 (1) - scopus: 2-s2.0-3042793356 (2)
11573/112808 - 2004 -
Polyvalvular heart disease associated with short stature, facial anomalies and mental retardation. Digilio M., C; Capolino, R; Marino Taussig De Bodonia, Bruno; Versacci, Paolo - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS. PART A (WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030) pp. 101-103 - issn: 1552-4825 - wos: WOS:000221179700021 (2) - scopus: 2-s2.0-3142743083 (2)
11573/112809 - 2004 -
Ellis-van Creveld syndrome with hydrometrocolpos is not linked to chromosome arm 4p or 20p. Digilio, M. C.; Torrente, I; Goodship, J. A.; Marino Taussig De Bodonia, Bruno; Novelli, G; Giannotti, A; Dallapiccola, B. - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS. PART A (WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030) pp. 319-323 - issn: 1552-4825 - wos: WOS:000220606800018 (4) - scopus: 2-s2.0-1842510650 (5)
11573/112804 - 2004 -
Better surgical prognosis for patients with complete atrioventricular septal defect and Down’s syndrome. Formigari, R; Di Donato R., M; Gargiulo, G; Di Carlo, D; Feltri, C; Picchio F., M; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: ANNALS OF THORACIC SURGERY ([Boston etc.]: [Little Brown & Co. etc.]) pp. 666-672 - issn: 0003-4975 - wos: WOS:000222999300046 (93) - scopus: 2-s2.0-3242816332 (97)
11573/112494 - 2004 -
Familial aggregation of genetically heterogeneous hypertrophic cardiomyopathy: a boy with LEOPARD syndrome due to PTPN11 mutation and his nonsyndromic father lacking PTPN11 mutations M., Cristina Digilio; Giuseppe, Pacileo; Anna, Sarkozy; Giuseppe, Limongelli; Emanuela, Conti; Fabiana, Cerrato; Marino Taussig De Bodonia, Bruno; Pizzuti, Antonio; R., Calabro'; Bruno, Dallapiccola - 01a Articolo in rivista
rivista: BIRTH DEFECTS RESEARCH. PART A, CLINICAL AND MOLECULAR TERATOLOGY (WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030) pp. 95-98 - issn: 1542-0752 - wos: WOS:000220013200007 (13) - scopus: 2-s2.0-10744221281 (15)
11573/112810 - 2004 -
In memoriam. Manolo Quero Jimenez (1941-2003). Marino Taussig De Bodonia, Bruno; Ballerini, L.; Calabro', R. - 01a Articolo in rivista
rivista: ITALIAN HEART JOURNAL. SUPPLEMENT (Roma : C.E.P.I. Centro editoriale pubblicitario italiano) pp. 829-831 - issn: 1129-4728 - wos: (0) - scopus: (0)
11573/112807 - 2004 -
Cardiac defects in Mexican children with down syndrome Marino Taussig De Bodonia, Bruno; Calcagni, G.; Digilio, M. C. - 01a Articolo in rivista
rivista: REVISTA ESPAÑOLA DE CARDIOLOGÍA (Ediciones Doyma SA:Travesera de Gracia 17-21, E 08021 Barcelona Spain:011 34 93 2000711, 011 34 93 4145706, EMAIL: suscripciones@doyma.es, INTERNET: http://www.doyma.es, Fax: 011 34 93 2091136) pp. 482- - issn: 0300-8932 - wos: WOS:000221700400015 (4) - scopus: 2-s2.0-2942724378 (4)
11573/112806 - 2004 -
Outcome in Down syndrome fetuses with cardiac anomalies Marino Taussig De Bodonia, Bruno; Luca, Diociaiuti; Giulio, Calcagni; Pierpaolo, Mastroiacovo - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS. PART A (WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030) pp. 101-102 - issn: 1552-4825 - wos: WOS:000222329000023 (3) - scopus: 2-s2.0-3042762350 (5)
11573/250600 - 2003 -
Correlation between PTPN11 gene mutations and congenital heart defects in Noonan and LEOPARD syndromes A., Sarkozy; E., Conti; D., Seripa; M. C., Digilio; N., Grifone; C., Tandoi; V. M., Fazio; V., Di Ciommo; Marino Taussig De Bodonia, Bruno; Pizzuti, Antonio; Dalla Piccola, Bruno - 01a Articolo in rivista
rivista: JOURNAL OF MEDICAL GENETICS (BMJ / British Medical Journal Publishing Group:PO Box 299, London WC1H 9TD United Kingdom:011 44 20 73836270, EMAIL: subscriptions@bmjgroup.com, INTERNET: http://www.bmjpg.com/bmj, Fax: 011 44 20 73836402) pp. 704-708 - issn: 0022-2593 - wos: WOS:000185177700011 (143) - scopus: 2-s2.0-0042329925 (162)
11573/112493 - 2003 -
Influence of chromosome 22q11.2 microdeletion on surgical outcome after treatment of tetralogy of fallot with pulmonary atresia. Adriano, Carotti; Marino Taussig De Bodonia, Bruno; Roberto M., Di Donato - 01a Articolo in rivista
rivista: JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY (New York: Elsevier
Orlando, FL: Mosby Year Book) pp. 1666-1667 - issn: 0022-5223 - wos: WOS:000186722600082 (21) - scopus: 2-s2.0-0345356345 (25)
11573/115824 - 2003 -
Nonsyndromic pulmonary valve stenosis and the PTPN11 gene Anna, Sarkozy; Emanuela, Conti; Marino Taussig De Bodonia, Bruno; Maria Cristina, Digilio; Vincenzo, Paoletti; Rita, Mingarelli; Giorgia, Esposito; Pizzuti, Antonio; Bruno, Dallapiccola - 01b Commento, Erratum, Replica e simili
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS. PART A (WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030) pp. 389-390 - issn: 1552-4825 - wos: WOS:000182400800016 (14) - scopus: 2-s2.0-0043180465 (14)
11573/112999 - 2003 -
DiGeorge subtypes of nonsyndromic conotruncal defects: evidence against a major role of TBX1 Gene Conti, E; Grifone, N; Sarkozy, A; Tandoi, C; Marino Taussig De Bodonia, Bruno; Digilio, Mc; Mingarelli, R; Pizzuti, Antonio; Dalla Piccola, Bruno - 01a Articolo in rivista
rivista: EUROPEAN JOURNAL OF HUMAN GENETICS (-NATURE PUBLISHING GROUP, MACMILLAN BUILDING, 4 CRINAN ST, LONDON, ENGLAND, N1 9XW
-S Karger AG:Allschwilerstrasse 10, CH-4009 Basel Switzerland:011 41 61 3061111, EMAIL: orders@karger.ch, INTERNET: http://www.karger.com, Fax: 011 41 61 3061234) pp. 349-351 - issn: 1018-4813 - wos: WOS:000182505800009 (43) - scopus: 2-s2.0-0038364111 (44)
11573/112487 - 2003 -
Screening for celiac disease in patients with deletion 22q11.2 (DiGeorge/Velo-cardial-Facial syndrome). Digilio M., C; Giannotti, A; Castro, M; Colostro, F; Ferretti, F; Marino Taussig De Bodonia, Bruno; Dallapiccola, B. - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS. PART A (WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030) pp. 286-288 - issn: 1552-4825 - wos: WOS:000184940500017 (20) - scopus: 2-s2.0-0042695819 (26)
11573/112489 - 2003 -
Truncus arteriosus and duplication 8p. Digilio, M. C.; Angioni, A; Giannotti, A; Dallapiccola, B; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS. PART A (WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030) pp. 79-81 - issn: 1552-4825 - wos: WOS:000184516600016 (6) - scopus: 2-s2.0-0042824089 (6)
11573/112491 - 2003 -
Postural anomaly of the head-neck-shoulder alignment in patients with deletion 22q11.2 (DiGeorge/velocardiofacial sindrome). Digilio, M. C.; Giannotti, A.; Dallapiccola, B.; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: CLINICAL GENETICS (Blackwell Munksgaard:PO Box 2148, Periodicals Department, DK-1016 Copenhagen K Denmark:011 45 33 755913, EMAIL: agentservices@oxon.blackwellpublishing.com, INTERNET: http://www.blackwellmunksgaard.com, Fax: 011 45 77 333377) pp. 447-448 - issn: 0009-9163 - wos: WOS:000186075200014 (0) - scopus: 2-s2.0-0242694044 (1)
11573/112998 - 2003 -
Spectrum of clinical variability in familial deletion 22q11.2: from full manifestation to extremely mild clinical anomalies Digilio, Mc; Angioni, A; De Santis, M; Lombardo, A; Giannotti, A; Dallapiccola, B; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: CLINICAL GENETICS (Blackwell Munksgaard:PO Box 2148, Periodicals Department, DK-1016 Copenhagen K Denmark:011 45 33 755913, EMAIL: agentservices@oxon.blackwellpublishing.com, INTERNET: http://www.blackwellmunksgaard.com, Fax: 011 45 77 333377) pp. 308-313 - issn: 0009-9163 - wos: WOS:000182322700018 (89) - scopus: 2-s2.0-0042632658 (99)
11573/112997 - 2003 -
Specific congenital heart defects in RSH/Smith-Lemli-Opitz syndrome: Postulated involvement of the sonic hedgehog pathway in syndromes with postaxial polydactyly or heterotaxia Maria Cristina, Digilio; Marino Taussig De Bodonia, Bruno; Aldo, Giannotti; Bruno, Dallapiccola; John M., Opitz - 01a Articolo in rivista
rivista: BIRTH DEFECTS RESEARCH. PART A, CLINICAL AND MOLECULAR TERATOLOGY (WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030) pp. 149-153 - issn: 1542-0752 - wos: WOS:000185286600001 (31) - scopus: 2-s2.0-0141891471 (36)
11573/112492 - 2003 -
Spiral pattern: universe, normal heart and complex congenital defects. Marino Taussig De Bodonia, Bruno; Corno, A. - 01a Articolo in rivista
rivista: JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY (New York: Elsevier
Orlando, FL: Mosby Year Book) pp. 1225-1226 - issn: 0022-5223 - wos: WOS:000365600900108 (0) - scopus: 2-s2.0-0142213779 (12)
11573/112488 - 2003 -
Tetralogy of Fallot with aortic valvular stenosis and deletion 22q11 Marino Taussig De Bodonia, Bruno; Federica, Mileto; M. C., Digilio - 01a Articolo in rivista
rivista: ANNALS OF THORACIC SURGERY ([Boston etc.]: [Little Brown & Co. etc.]) pp. 2010-2011 - issn: 0003-4975 - wos: WOS:000183311400088 (6) - scopus: 2-s2.0-0038650898 (5)
11573/255750 - 2003 -
Biased T-cell receptor repertoires in patienys with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome) Pierdominici, M; Mazzetta, F; Caprini, E; Marziali, M; Digilio, Mc; Marino Taussig De Bodonia, Bruno; Aiuti, A; Amati, F; Russo, G; Novelli, G; Pandolfi, F; Luzi, Giuseppe; Giovannetti, A. - 01a Articolo in rivista
rivista: CLINICAL AND EXPERIMENTAL IMMUNOLOGY (Blackwell Science Limited:PO Box 88, Oxford OX2 0NE United Kingdom:011 44 1865 776868, 011 44 1865 206038, EMAIL: journals.cs@blacksci.co.uk, INTERNET: http://www.blackwell-science.com, Fax: 011 44 1865 721205) pp. 323-331 - issn: 0009-9104 - wos: WOS:000182305500022 (52) - scopus: 2-s2.0-0038216872 (57)
11573/254008 - 2003 -
Mutations of FOG-2 gene in sporadic cases of Tetralogy of Fallot Pizzuti, Antonio; Sarkozy, A; Newton, Al; Conti, E; Flex, E; Digilio, Mc; Amati, F; Gianni, D; Tandoi, C; Marino Taussig De Bodonia, Bruno; Crossley, M; Dalla Piccola, Bruno - 01a Articolo in rivista
rivista: HUMAN MUTATION (John Wiley & Sons Incorporated:Customer Service, 111 River Street:Hoboken, NJ 07030:(800)225-5945, (201)748-6000, EMAIL: societyinfo@wiley.com, INTERNET: http://www.wiley.com, Fax: (212)748-6551) pp. 372-3777 - issn: 1059-7794 - wos: WOS:000244273200001 (28) - scopus: 2-s2.0-33847294697 (33)
11573/254642 - 2002 -
Grouping of multiple-lentigines/LEOPARD and Noonan syndromes on the PTPN11 gene Maria Cristina, Digilio; Emanuela, Conti; Anna, Sarkozy; Rita, Mingarelli; Tania, Dottorini; Marino Taussig De Bodonia, Bruno; Pizzuti, Antonio; Dalla Piccola, Bruno - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF HUMAN GENETICS (University of Chicago Press:PO Box 37005, Journals Division:Chicago, IL 60637:(877)705-1878, (877)705-1878, (773)753-2247, EMAIL: subscriptions@press.uchicago.edu, INTERNET: http://www.press.uchicago.edu, Fax: (877)705-1879, (773)753-0811) pp. 389-394 - issn: 0002-9297 - wos: WOS:000176977700016 (276) - scopus: 2-s2.0-0036074033 (332)
11573/112483 - 2002 -
Transposition of the great arteries in asplenia and polysplenia phenotypes Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS (John Wiley & Sons Incorporated:Customer Service, 111 River Street:Hoboken, NJ 07030:(800)225-5945, (201)748-6000, EMAIL: societyinfo@wiley.com, INTERNET: http://www.wiley.com, Fax: (212)748-6551) pp. 292-294 - issn: 0148-7299 - wos: WOS:000176273900017 (23) - scopus: 2-s2.0-0036644186 (26)
11573/541390 - 2002 -
Transposition of the great arteries. Some gleams of light to pathogenetic knowledge Marino Taussig De Bodonia, Bruno; M. C., Digilio; Versacci, Paolo; S., Anaclerio; B., Dallapiccola - 01a Articolo in rivista
rivista: ITALIAN HEART JOURNAL. SUPPLEMENT (Roma : C.E.P.I. Centro editoriale pubblicitario italiano) pp. 154-160 - issn: 1129-4728 - wos: (0) - scopus: 2-s2.0-0036227522 (7)
11573/112484 - 2002 -
Criss-Cross heart with d-ventricular loop Marino Taussig De Bodonia, Bruno; Mileto, F. - 01a Articolo in rivista
rivista: CIRCULATION (Philadelphia, PA: Lippincott, Williams & Wilkins) pp. 223-223 - issn: 0009-7322 - wos: WOS:000180045800008 (2) - scopus: 2-s2.0-0037126524 (4)
11573/113275 - 2002 -
Pulmonary atresia with intact ventricular septum and systemic-pulmonary collateral arteries Sonia B., Albanese; Adriano, Carotti; Alessandra, Toscano; Marino Taussig De Bodonia, Bruno; Roberto M., Di Donato - 01a Articolo in rivista
rivista: ANNALS OF THORACIC SURGERY ([Boston etc.]: [Little Brown & Co. etc.]) pp. 1322-1324 - issn: 0003-4975 - wos: WOS:000174807400081 (5) - scopus: 2-s2.0-0036211434 (9)
11573/111600 - 2002 -
Ventricular septal defect and deletion of chromosome 22q11: anatomically types and aortic arch anomalies Toscano, A; Anaclerio, S; Digilio, Mc; Giannotti, A; Fariello, G; Dallapiccola, B; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: EUROPEAN JOURNAL OF PEDIATRICS (Springer Verlag Germany:Tiergartenstrasse 17, D 69121 Heidelberg Germany:011 49 6221 3450, EMAIL: g.braun@springer.de, INTERNET: http://www.springer.de, Fax: 011 49 6221 345229) pp. 116-117 - issn: 0340-6199 - wos: WOS:000174127800011 (17) - scopus: 2-s2.0-0036167391 (19)
11573/53197 - 2002 -
NOONAN SYNDROME AND TURNER SYNDROME: OVERLAP OF CARDIAC PHENOTYPES. Versacci, P.; Ventriglia, F.; Bosco, Giovanna; Anaclerio, S.; Pucarelli, I.; Pasquino, A. M.; Diglio, M. C.; Marino Taussig De Bodonia, Bruno - 04a Atto di comunicazione a congresso
libro: XXXII CONGRESSO NAZIONALE SICP - ()
11573/255934 - 2001 -
Complete transposition of the great arteries: patterns of congenital heart disease in familial precurrence Digilio, M. C.; Casey, B.; Toscano, A.; Calabro', R.; Pacileo, G.; Marasini, M.; Banaudi, E.; Giannotti, A.; Dalla Piccola, Bruno; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: CIRCULATION (Philadelphia, PA: Lippincott, Williams & Wilkins) pp. 2809-2814 - issn: 0009-7322 - wos: WOS:000172577400013 (75) - scopus: 2-s2.0-0035808021 (93)
11573/112995 - 2001 -
Congenital heart defects in Kabuki syndrome Maria Cristina, Digilio; Marino Taussig De Bodonia, Bruno; Alessandra, Toscano; Aldo, Giannotti; Bruno, Dallapiccola - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS (John Wiley & Sons Incorporated:Customer Service, 111 River Street:Hoboken, NJ 07030:(800)225-5945, (201)748-6000, EMAIL: societyinfo@wiley.com, INTERNET: http://www.wiley.com, Fax: (212)748-6551) pp. 269-274 - issn: 0148-7299 - wos: WOS:000168268200004 (83) - scopus: 2-s2.0-0035874017 (104)
11573/112994 - 2001 -
Genetic predisposition to ventricular septal defect in Down syndrome Maria, Digilio; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: HUMAN GENETICS (Germany: Springer Verlag Germany) pp. 463-463 - issn: 0340-6717 - wos: WOS:000172350700011 (3) - scopus: 2-s2.0-0035167638 (2)
11573/112993 - 2001 -
Age at operation for children with atrioventricular canal. Marino Taussig De Bodonia, Bruno; Anaclerio, S.; Di Donato, R. - 01a Articolo in rivista
rivista: PEDIATRICS (American Academy of Pediatrics:141 Northwest Point Boulevard:Elk Grove Village, IL 60007:(800)433-9016, (847)434-4000, EMAIL: journals@aap.org, INTERNET: http://www.aap.org, Fax: (847)434-8000) pp. 217-217 - issn: 0031-4005 - wos: WOS:000169571400064 (0) - scopus: 2-s2.0-17844381298 (1)
11573/112482 - 2001 -
Health supervision for children with down syndrome. Marino Taussig De Bodonia, Bruno; Digilio, Mc; Di Donato, R. - 01a Articolo in rivista
rivista: PEDIATRICS (American Academy of Pediatrics:141 Northwest Point Boulevard:Elk Grove Village, IL 60007:(800)433-9016, (847)434-4000, EMAIL: journals@aap.org, INTERNET: http://www.aap.org, Fax: (847)434-8000) pp. 1384-1385 - issn: 0031-4005 - wos: WOS:000172498000047 (8) - scopus: 2-s2.0-0035650741 (16)
11573/112992 - 2000 -
Loss-of-function mutations in the EGF-GFC gene CFC1 are associated with human left-right lateraility defects. Bamford, Rn; Roessler, R; Burdine, Rd; U., Saplakoglu; J., De La Cruz; M., Splitt; J., Towbin; P., Bowers; Marino Taussig De Bodonia, Bruno; Af, Schier; Mm, Shen; M., Muenke; Casey, B. - 01a Articolo in rivista
rivista: NATURE GENETICS (Nature America Incorporated:345 Park Avenue South, 6th Floor:New York, NY 10010:(888)331-6288, EMAIL: institutions@natureny.com, INTERNET: http://www.nature.com, Fax: (212)689-9108) pp. 365-9 - issn: 1061-4036 - wos: WOS:000165176500031 (258) - scopus: 2-s2.0-0033768239 (293)
11573/113271 - 2000 -
Familial recurrence of nonsyndromic interrupted aortic arch and truncus arteriosus with atrioventricular canal. Digilio, Mc; Marino Taussig De Bodonia, Bruno; Musolino, Am; Giannotti, A; Dallapiccola, B. - 01a Articolo in rivista
rivista: TERATOLOGY (John Wiley & Sons Incorporated:Customer Service, 111 River Street:Hoboken, NJ 07030:(800)225-5945, (201)748-6000, EMAIL: societyinfo@wiley.com, INTERNET: http://www.wiley.com, Fax: (212)748-6551) pp. 329-331 - issn: 0040-3709 - wos: WOS:000086815900003 (9) - scopus: 2-s2.0-0034021815 (15)
11573/112989 - 2000 -
Clinical and cardiorespiratory assessment in children with Down syndrome without congenital heart disease. E., Pastore; Marino Taussig De Bodonia, Bruno; A., Calzolari; Mc, Digilio; A., Giannotti; B., Dallapiccola; A., Turchetta - 01a Articolo in rivista
rivista: ARCHIVES OF PEDIATRICS & ADOLESCENT MEDICINE (American Medical Association:515 North State Street:Chicago, IL 60610:(800)262-2350, (312)464-2518, EMAIL: ama-subs@ama-assn.org, INTERNET: http://www.ama-assn.org, Fax: (312)464-5600) pp. 408-10 - issn: 1072-4710 - wos: WOS:000086366400016 (32) - scopus: 2-s2.0-0034075633 (41)
11573/256289 - 2000 -
Deletion af a 5 cM region at chromosome 8p23 is associated with a spectrum of congenital heart defects. Giglio, S; Graw, Sl; Gimelli, G; Pirola, B; Varone, P; Voullaire, L; Lerzo, F; Rossi, E; Dellavecchia, C; Bonaglia, Mc; Digilio, Mc; Giannotti, A; Marino Taussig De Bodonia, Bruno; Carrozzo, R; Korenberg, Jr; Danesino, C; Sujansky, E; Dalla Piccola, Bruno; Zuffardi, O. - 01a Articolo in rivista
rivista: CIRCULATION (Philadelphia, PA: Lippincott, Williams & Wilkins) pp. 432-437 - issn: 0009-7322 - wos: WOS:000088374400020 (66) - scopus: 2-s2.0-0034713818 (78)
11573/113273 - 2000 -
Heterotaxy with left atrial isomerism in a patient with deletion 18p Maria Cristina, Digilio; Marino Taussig De Bodonia, Bruno; Aldo, Giannotti; Roberto Di, Donato; Bruno, Dallapiccola - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS (John Wiley & Sons Incorporated:Customer Service, 111 River Street:Hoboken, NJ 07030:(800)225-5945, (201)748-6000, EMAIL: societyinfo@wiley.com, INTERNET: http://www.wiley.com, Fax: (212)748-6551) pp. 198-200 - issn: 0148-7299 - wos: WOS:000089022800004 (20) - scopus: 2-s2.0-0034684042 (20)
11573/112988 - 2000 -
Congenital heart disease and genetic syndromes: specific correlation between cardiac phenotype and genotype. Marino Taussig De Bodonia, Bruno; Mc, Digilio - 01a Articolo in rivista
rivista: CARDIOVASCULAR PATHOLOGY (Elsevier Science Incorporated / NY Journals:Madison Square Station, PO Box 882:New York, NY 10159:(212)633-3730, EMAIL: usinfo-f@elsevier.com, INTERNET: http://www.elsevier.com, Fax: (212)633-3680) pp. 303-15 - issn: 1054-8807 - wos: WOS:000166034100001 (72) - scopus: 2-s2.0-0034538594 (94)
11573/255735 - 2000 -
T cell receptor repertoire and function in patients with DiGeroge syndrome and velocardiofacial syndrome Pierdominici, M; Marziali, M; Giovannetti, A; Rosso, R; Marino Taussig De Bodonia, Bruno; Digilio, Mc; Giannotti, A; Novelli, G; Dallapiccola, B; Aiuti, Fernando; Pandolfi, F. - 01a Articolo in rivista
rivista: CLINICAL AND EXPERIMENTAL IMMUNOLOGY (Blackwell Science Limited:PO Box 88, Oxford OX2 0NE United Kingdom:011 44 1865 776868, 011 44 1865 206038, EMAIL: journals.cs@blacksci.co.uk, INTERNET: http://www.blackwell-science.com, Fax: 011 44 1865 721205) pp. 127-132 - issn: 0009-9104 - wos: WOS:000087856600019 (26) - scopus: 2-s2.0-0033919852 (32)
11573/256453 - 2000 -
Mutations in a novel gene in Ellis-van Creveld syndrome and Weyers acrofacial dysostosis. Vl Ruiz, Perez; Se, Ide; Tm, Strom; B., Lorenz; D., Wilson; K., Woods; L., King; C., Francomano; P., Freisenger; S., Spranger; Marino Taussig De Bodonia, Bruno; Dalla Piccola, Bruno - 01a Articolo in rivista
rivista: NATURE GENETICS (Nature America Incorporated:345 Park Avenue South, 6th Floor:New York, NY 10010:(888)331-6288, EMAIL: institutions@natureny.com, INTERNET: http://www.nature.com, Fax: (212)689-9108) pp. 283-286 - issn: 1061-4036 - wos: WOS:000085590600021 (223) - scopus: 2-s2.0-0034104297 (264)
11573/113270 - 1999 -
Atypical deletions suggest five 22q11.2 critical regions related to the DiGeorge/VCF syndrome. Amati, F; Conti, E; Novelli, A; Bengala, M; Digilio, Mc; Marino Taussig De Bodonia, Bruno; Giannotti, A; Gabrielli, O; Novelli, G; Dallapiccola, B. - 01a Articolo in rivista
rivista: EUROPEAN JOURNAL OF HUMAN GENETICS (-NATURE PUBLISHING GROUP, MACMILLAN BUILDING, 4 CRINAN ST, LONDON, ENGLAND, N1 9XW
-S Karger AG:Allschwilerstrasse 10, CH-4009 Basel Switzerland:011 41 61 3061111, EMAIL: orders@karger.ch, INTERNET: http://www.karger.com, Fax: 011 41 61 3061234) pp. 903-909 - issn: 1018-4813 - wos: WOS:000084715800008 (66) - scopus: 2-s2.0-0033380870 (68)
11573/113266 - 1999 -
Cardiac malformations in patients with oral-facial-skeletal syndromes: clinical similarities with heterotaxia Digilio, Mc; Marino Taussig De Bodonia, Bruno; Ammirati, A; Borzaga, U; Giannotti, A; Dallapiccola, B. - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS (John Wiley & Sons Incorporated:Customer Service, 111 River Street:Hoboken, NJ 07030:(800)225-5945, (201)748-6000, EMAIL: societyinfo@wiley.com, INTERNET: http://www.wiley.com, Fax: (212)748-6551) pp. 350-356 - issn: 0148-7299 - wos: WOS:000080037200008 (71) - scopus: 2-s2.0-0033522782 (76)
11573/112480 - 1999 -
Genetic heterogenity of isolated noncompaction of the left ventricular myocardium Digilio, Mc; Marino Taussig De Bodonia, Bruno; Bevilacqua, M; Musolino, Am; Giannotti, A; Dallapiccola, B. - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS (John Wiley & Sons Incorporated:Customer Service, 111 River Street:Hoboken, NJ 07030:(800)225-5945, (201)748-6000, EMAIL: societyinfo@wiley.com, INTERNET: http://www.wiley.com, Fax: (212)748-6551) pp. 90-91 - issn: 0148-7299 - wos: WOS:000080650900019 (39) - scopus: 2-s2.0-0033516626 (41)
11573/113268 - 1999 -
Atrioventricular canal defect and hypoplastic left heart syndrome as discirdant congenital heart defects in twins. Digilio, Mc; Marino Taussig De Bodonia, Bruno; Giannico, S; Giannotti, A; Dallapiccola, B. - 01a Articolo in rivista
rivista: TERATOLOGY (John Wiley & Sons Incorporated:Customer Service, 111 River Street:Hoboken, NJ 07030:(800)225-5945, (201)748-6000, EMAIL: societyinfo@wiley.com, INTERNET: http://www.wiley.com, Fax: (212)748-6551) pp. 206-208 - issn: 0040-3709 - wos: WOS:000082964400004 (6) - scopus: 2-s2.0-0032869217 (6)
11573/113267 - 1999 -
Atrioventricular canal defect without Down syndrome: a heterogeneous malformations. Digilio, Mc; Marino Taussig De Bodonia, Bruno; Toscano, A; Giannotti, A; Dallapiccola, B. - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS (John Wiley & Sons Incorporated:Customer Service, 111 River Street:Hoboken, NJ 07030:(800)225-5945, (201)748-6000, EMAIL: societyinfo@wiley.com, INTERNET: http://www.wiley.com, Fax: (212)748-6551) pp. 140-146 - issn: 0148-7299 - wos: WOS:000081010100008 (61) - scopus: 2-s2.0-0032999573 (66)
11573/113269 - 1999 -
Audiological findings in patients with microdeletions 22q11 (DiGeorge/velocardiofacial syndrome) Digilio, Mc; Pacifico, C; Tieri, L; Marino Taussig De Bodonia, Bruno; Giannotti, A; Dallapiccola, B. - 01a Articolo in rivista
rivista: BRITISH JOURNAL OF AUDIOLOGY (London: Whurr Publishers.) pp. 324-329 - issn: 0300-5364 - wos: WOS:000084608800009 (51) - scopus: 2-s2.0-0033401203 (57)
11573/112479 - 1999 -
Guidelines for 22q11 deletion screening of patients with conotruncal defects M. C., Digilio; Marino Taussig De Bodonia, Bruno; A., Giannotti; R., Mingarelli; B., Dallapiccola - 01a Articolo in rivista
rivista: JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY ([New York N.Y.]: Elsevier Biomedical
Philadelphia, PA: W B Saunders Company) pp. 1746-1747 - issn: 0735-1097 - wos: WOS:000081122700049 (15) - scopus: 2-s2.0-0032709613 (16)
11573/113265 - 1999 -
Microdeletion 22q11 and oesophageal atresia M. C., Digilio; Marino Taussig De Bodonia, Bruno; P., Bagolan; A., Giannotti; B., Dallapiccola - 01a Articolo in rivista
rivista: JOURNAL OF MEDICAL GENETICS (BMJ / British Medical Journal Publishing Group:PO Box 299, London WC1H 9TD United Kingdom:011 44 20 73836270, EMAIL: subscriptions@bmjgroup.com, INTERNET: http://www.bmjpg.com/bmj, Fax: 011 44 20 73836402) pp. 137-139 - issn: 0022-2593 - wos: WOS:000078450100011 (45) - scopus: 2-s2.0-0032993107 (58)
11573/112481 - 1999 -
Inlet ventricular septal defect is not a partial atrioventricular septal defect. Marino Taussig De Bodonia, Bruno; M. C., Digilio - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS (John Wiley & Sons Incorporated:Customer Service, 111 River Street:Hoboken, NJ 07030:(800)225-5945, (201)748-6000, EMAIL: societyinfo@wiley.com, INTERNET: http://www.wiley.com, Fax: (212)748-6551) pp. 195-195 - issn: 0148-7299 - wos: WOS:000083558800013 (1) - scopus: 2-s2.0-0032707126 (2)
11573/247007 - 1999 -
Congenital heart diseases in children with Noonan syndrome: An expanded cardiac spectrum with high prevalence of atrioventricular canal Marino Taussig De Bodonia, Bruno; Maria Cristina, Digilio; Alessandra, Toscano; Aldo, Giannotti; Dalla Piccola, Bruno - 01a Articolo in rivista
rivista: THE JOURNAL OF PEDIATRICS (New York NY: Elsevier
St. Louis Mo.: C.V. Mosby) pp. 703-706 - issn: 0022-3476 - wos: WOS:000084263700016 (175) - scopus: 2-s2.0-0033498871 (205)
11573/112987 - 1999 -
Deletion 22q11 in patients with interrupted aortic arch. Marino Taussig De Bodonia, Bruno; Mc, Digilio; M., Persiani; R., Di Donato; A., Toscano; A., Giannotti; B., Dallapiccola - 01a Articolo in rivista
rivista: THE AMERICAN JOURNAL OF CARDIOLOGY (NY : Elsevier Science Incorporated /
NY; EXCERPTA MEDICA INC) pp. 360-1 - issn: 0002-9149 - wos: WOS:000081680600027 (33) - scopus: 2-s2.0-0033180446 (44)
Digilio, Mc; Marino Taussig De Bodonia, Bruno; Guccione, P; Giannotti, A; Mingarelli, R; Dallapiccola, B. - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS (John Wiley & Sons Incorporated:Customer Service, 111 River Street:Hoboken, NJ 07030:(800)225-5945, (201)748-6000, EMAIL: societyinfo@wiley.com, INTERNET: http://www.wiley.com, Fax: (212)748-6551) pp. 534-536 - issn: 0148-7299 - wos: WOS:000071809100015 (58) - scopus: 2-s2.0-0032539490 (63)
11573/113054 - 1998 -
Noonan syndrome and aortic coarctation. Digilio, Mc; Marino Taussig De Bodonia, Bruno; Picchio, F; Prandstraller, B; Toscano, A; Giannotti, A; Dallapiccola, B. - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS (John Wiley & Sons Incorporated:Customer Service, 111 River Street:Hoboken, NJ 07030:(800)225-5945, (201)748-6000, EMAIL: societyinfo@wiley.com, INTERNET: http://www.wiley.com, Fax: (212)748-6551) pp. 160-162 - issn: 0148-7299 - wos: WOS:000076615600013 (32) - scopus: 2-s2.0-0031790484 (38)
11573/113264 - 1998 -
Congenital heart defect in sibs with discordant karyotypes M. C., Digilio; Marino Taussig De Bodonia, Bruno; S. A., Capena; U., Borzaga; A., Giannotti; B., Dallapiccola - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS (John Wiley & Sons Incorporated:Customer Service, 111 River Street:Hoboken, NJ 07030:(800)225-5945, (201)748-6000, EMAIL: societyinfo@wiley.com, INTERNET: http://www.wiley.com, Fax: (212)748-6551) pp. 169-172 - issn: 0148-7299 - wos: WOS:000076615600015 (10) - scopus: 2-s2.0-0031732657 (14)
11573/256885 - 1998 -
Familial recurrence of transposition of the great arteries. Maria Cristina, Digilio; Marino Taussig De Bodonia, Bruno; Elena, Banaudi; Maurizio, Marasini; Dalla Piccola, Bruno - 01a Articolo in rivista
rivista: THE LANCET (Lancet Limited:42 Bedford Square, London WC1B 3SL United Kingdom:011 44 207 4364981, EMAIL: custserv@lancet.com, INTERNET: http://www.thelancet.com, Fax: 011 44 207 3236433) pp. 1661-1661 - issn: 0140-6736 - wos: WOS:000074026600051 (5) - scopus: 2-s2.0-0032580702 (7)
11573/113333 - 1998 -
Severe truncal valve dysplasia: Association with DiGeorge syndrome? Marino Taussig De Bodonia, Bruno; M. C., Digilio; B., Dallapiccola - 01a Articolo in rivista
rivista: ANNALS OF THORACIC SURGERY ([Boston etc.]: [Little Brown & Co. etc.]) pp. 980-980 - issn: 0003-4975 - wos: WOS:000076166100089 (17) - scopus: 2-s2.0-0031656606 (25)
11573/23582 - 1997 -
A genetic assessment of trisomy 21 in a patient with persistent truncus arteriosus who died 38 years ago Francalanci, P; Gallo, Pietro; Dalla Piccola, Bruno; Calabrese, G; Marino Taussig De Bodonia, Bruno - 01a Articolo in rivista
rivista: THE AMERICAN JOURNAL OF CARDIOLOGY (NY : Elsevier Science Incorporated /
NY; EXCERPTA MEDICA INC) pp. 245-247 - issn: 0002-9149 - wos: WOS:A1997WC65100033 (2) - scopus: 2-s2.0-0031567858 (5)
11573/1656846 - 1996 -
Return to work and quality of life measurement in coronary artery bypass grafting. Speziale, G; Bilotta, F; Ruvolo, G; Fattouch, K; Marino, B. - 01a Articolo in rivista
rivista: EUROPEAN JOURNAL OF CARDIO-THORACIC SURGERY ([S.l.] : Elsevier Science) pp. 852-858 - issn: 1873-734X - wos: (0) - scopus: (0)
11573/1656819 - 1995 -
Low-dose dobutamine echocardiography predicts the early response of dysfunctioning myocardial segments to coronary artery bypass grafting Voci, P; Bilotta, F; Caretta, Q; Mercanti, C; Marino, B - 01a Articolo in rivista
rivista: AMERICAN HEART JOURNAL (St. Louis: Elsevier [etc.]) pp. 521-526 - issn: 0002-8703 - wos: (0) - scopus: (0)
11573/1656861 - 1995 -
Papillary muscle perfusion pattern. A hypothesis for ischemic papillary muscle dysfunction. Voci, P; Bilotta, F; Caretta, Q; Mercanti, C; Marino, B. - 01a Articolo in rivista
rivista: CIRCULATION (Philadelphia, PA: Lippincott, Williams & Wilkins) pp. 1714-1718 - issn: 0009-7322 - wos: (0) - scopus: (0)
11573/1656820 - 1994 -
Intraoperative detection of coronary graft occlusion by myocardial contrast echocardiography Caretta, Q; Voci, P; Bilotta, F; Mercanti, C; Marino, B - 01a Articolo in rivista
rivista: JOURNAL OF CARDIOTHORACIC AND VASCULAR ANESTHESIA (W B Saunders Company:Fulfillment Department, The Curtis Center, Independence Square West:Philadelphia, PA 19106:(800)654-2452, (215)238-7800, EMAIL: wbspcs@harcourt.com, INTERNET: http://elsevierhealth.com, Fax: (215)238-6445) pp. 206-208 - issn: 1053-0770 - wos: (0) - scopus: (0)
11573/1656840 - 1993 -
Mechanisms of incomplete cardioplegia distribution during coronary artery surgery: an intraoperative transesophageal contrast echocardiography study Voci, P; Bilotta, F; Caretta, Q; Mercanti, C; Marino, B - 01a Articolo in rivista
rivista: ANESTHESIOLOGY ([Philadelphia Pa.]: [American Society of Anesthesiologists etc.]Fax: (215)238-4227) pp. 904-912 - issn: 0003-3022 - wos: (0) - scopus: (0)
11573/1656869 - 1992 -
Echocardiographic analysis of dysfunctional and normal myocardial segments before and immediately after coronary artery bypass surgery Voci, P; Bilotta, F; Aronson, S; Scibilia, G; Caretta, Q; Mercanti, C; Marino, B; Thiested, R; Roizen, Mf; Reale, A - 01a Articolo in rivista
rivista: ANESTHESIA AND ANALGESIA (Baltimore MD: Williams & Wilkins) pp. 213-218 - issn: 0003-2999 - wos: (0) - scopus: (0)
11573/414033 - 1991 -
Comparison of left ventricular ejection fraction by magnetic resonance imaging and radionuclide ventriculography in idiopathic dilated cardiomyopathy Gaudio, Carlo; Tanzilli, Gaetano; Mazzarotto, P.; Motolese, M.; Romeo, F.; Marino, B.; Reale, A. - 01a Articolo in rivista
rivista: THE AMERICAN JOURNAL OF CARDIOLOGY (NY : Elsevier Science Incorporated /
NY; EXCERPTA MEDICA INC) pp. - - issn: 0002-9149 - wos: WOS:A1991EX48700014 (43) - scopus: 2-s2.0-0025982114 (44)
11573/1656875 - 1991 -
Spontaneous left atrial echo contrast in mitral stenosis: disappearance after valve replacement Voci, P; Bilotta, F; Maugeri, B; Caretta, Q; Mercanti, C; Marino, B; Reale, A - 01a Articolo in rivista
rivista: JOURNAL OF THE AMERICAN SOCIETY OF ECHOCARDIOGRAPHY (Mosby Year Book Incorporated:6277 Sea Harbor Drive:Orlando, FL 32887:(800)654-2452, (407)345-4000, EMAIL: hhspcs@harcourt.com, INTERNET: http://www.mosby.com, Fax: (407)363-9661, (314)432-1380) pp. 648-65' - issn: 0894-7317 - wos: (0) - scopus: (0)
11573/1656872 - 1991 -
In-vitro development and clinical applications of sonicated echocontrast agents Voci, P; Bilotta, F; Scibilia, G; Mercanti, C; Caretta, Q; Marino, B; Reale, A - 01a Articolo in rivista
rivista: AMERICAN JOURNAL OF CARDIAC IMAGING (-Philadelphia Pa W.B. Saunders Co.
-Orlando, FL] : Grune & Stratton, [c1987-1996]) pp. 192-199. - issn: 0887-7971 - wos: (0) - scopus: (0)
11573/377620 - 1990 -
Post inflammatory scarring of Cardiac valves of rheumatic and no rheumatic aetiology P., Gallo; Tonelli, Euclide; U., Papalia; D'amati, Giulia; Marino, B. - 01a Articolo in rivista
rivista: THE AMERICAN JOURNAL OF CARDIOVASCULAR PATHOLOGY (Field & Wood Publishers:155 East Bettlewood Avenue:Oaklyn, NJ 08107:(610)828-4010, Fax: (215)482-0226) pp. - - issn: 0887-8005 - wos: (0) - scopus: (0)
11573/377773 - 1984 -
Un ossigenatore per circolazione extracorporea in piccoli animali Toscano, Michele; R., Chiavarelli; Tonelli, Euclide; Marino, B. - 01a Articolo in rivista
rivista: ARCHIVIO DI CHIRURGIA TORACICA E CARDIOVASCOLARE (Rome Italy Edizioni Luigi Pozzi Srl) pp. - - issn: 0391-7029 - wos: (0) - scopus: (0)
11573/377774 - 1984 -
Protezione miocardica in presenza di ostruzioni coronariche: somministrazione di soluzione cardioplegica via seno coronario. Toscano, Michele; R., Chiavarelli; Tonelli, Euclide; Marino, B. - 01a Articolo in rivista
rivista: RIVISTA GENERALE ITALIANA DI CHIRURGIA (Casa Editrice Maccari:via Trento 53, 43100 Parma Italy:011 39 521 771268, Fax: 011 39 521 771268) pp. - - issn: 0035-6689 - wos: (0) - scopus: (0)
11573/22254 - 1980 -
Profilo anatomo-clinico dell'atresia aortica con difetto interventricolare Marino Taussig De Bodonia, Bruno; Thiene, G; Bosman, Cesare; Milanesi, O; Gallo, Pietro; Pellegrino, Pa - 01a Articolo in rivista
rivista: REVISTA LATINA DE CARDIOLOGIA (IDEPSA International Ediciones y Publicaciones SA:Principe de Vergara 112 1F, 28002 Madrid Spain:011 34 1 5637306, Fax: 011 34 1 5632393) pp. 108-115 - issn: 0210-8755 - wos: (0) - scopus: (0)