11573/1706833 - 2024 -
From Klinefelter Syndrome to High Grade Aneuploidies: Expanding the Gene-dosage Effect of Supernumerary X Chromosomes Spaziani, Matteo; Carlomagno, Francesco; Tarantino, Chiara; Angelini, Francesco; Paparella, Roberto; Tarani, Luigi; Putotto, Carolina; Badagliacca, Roberto; Pozza, Carlotta; Isidori, Andrea; Gianfrilli, Daniele - 01a Articolo in rivista
paper: THE JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (Baltimore, MD : Endocrine Society) pp. - - issn: 1945-7197 - wos: WOS:001138268000001 (4) - scopus: (0)
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
paper: 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
paper: GENES (Basel : Molecular Diversity Preservation International) pp. 160- - issn: 2073-4425 - wos: WOS:000915190100001 (11) - scopus: 2-s2.0-85146758210 (13)
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
paper: 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
paper: JOURNAL OF NEUROPSYCHOLOGY ([Leicester] : British Psychological Society) pp. 564-583 - issn: 1748-6653 - wos: WOS:000985648300001 (0) - scopus: 2-s2.0-85158990260 (0)
11573/1702818 - 2023 -
Prenatal vs postnatal diagnosis of 22q11.2 deletion syndrome: cardiac and noncardiac outcomes through 1 year of age Freud, Lindsay R.; Galloway, Stephanie; Crowley, T. Blaine; Moldenhauer, Julie; Swillen, Ann; Breckpot, Jeroen; Borrell, Antoni; Vora, Neeta L.; Cuneo, Bettina; Hoffman, Hilary; Gilbert, Lisa; Nowakowska, Beata; Geremek, Maciej; Kutkowska-Kaźmierczak, Anna; Vermeesch, Joris R.; Devriendt, Koen; Busa, Tiffany; Sigaudy, Sabine; Vigneswaran, Trisha; Simpson, John M.; Dungan, Jeffrey; Gotteiner, Nina; Gloning, Karl-Philipp; Digilio, Maria Cristina; Unolt, Marta; Putotto, Carolina; Marino, Bruno; Repetto, Gabriela; Fadic, Magdalena; Garcia-Minaur, Sixto; Achón Buil, Ana; Thomas, Mary Ann; Fruitman, Deborah; Beecroft, Taylor; Hui, Pui Wah; Oskarsdottir, Solveig; Bradshaw, Rachael; Criebaum, Amanda; Norton, Mary E.; Lee, Tiffany; Geiger, Miwa; Dunnington, Leslie; Isaac, Jacqueline; Wilkins-Haug, Louise; Hunter, Lindsey; Izzi, Claudia; Toscano, Marika; Ghi, Tullio; Mcglynn, Julie; Romana Grati, Francesca; Emanuel, Beverly S.; Gaiser, Kimberly; Gaynor, J. William; Goldmuntz, Elizabeth; Mcginn, Daniel E.; Schindewolf, Erica; Tran, Oanh; Zackai, Elaine H.; Yan, Qi; Bassett, Anne S.; Wapner, Ronald; Mcdonald-Mcginn, Donna M. - 01a Articolo in rivista
paper: AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY (St. Louis: C.V. Mosby Co.
Latest publisher: New York: Elsevier) pp. - - issn: 0002-9378 - wos: WOS:001203611200001 (2) - scopus: 2-s2.0-85174044190 (2)
11573/1679501 - 2023 -
Neuroinflammation and Oxidative Stress in Individuals Affected by DiGeorge Syndrome Menghi, Michela; Micangeli, Ginevra; Tarani, Francesca; Putotto, Carolina; Pirro, Federica Anna; Mariani, Alessandro; Petrella, Carla; Pulvirenti, Federica; Cinicola, Bianca Laura; Colloridi, Fiorenza; Tarani, Luigi; Fiore, Marco - 01a Articolo in rivista
paper: INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (Basel: MDPI Center) pp. 4242- - issn: 1422-0067 - wos: WOS:000939072700001 (2) - scopus: 2-s2.0-85149021489 (1)
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
paper: GENETICS IN MEDICINE (New York: Elsevier Inc.
Baltimore MD: Lippincott Williams & Wilkins) pp. 100338- - issn: 1530-0366 - wos: WOS:001029315800001 (15) - scopus: 2-s2.0-85146771243 (22)
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
paper: 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 (2) - 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
paper: 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)
paper: THE ANATOMICAL RECORD (Hoboken, NJ : John Wiley & Sons, 2007-) pp. 502-514 - issn: 1932-8486 - wos: WOS:000895829700001 (1) - scopus: 2-s2.0-85144067123 (1)
11573/1680334 - 2023 -
Neuroimmune dysregulation in prepubertal and adolescent individuals affected by Klinefelter syndrome Tarani, Luigi; Ceci, Flavio Maria; Carito, Valentina; Ferraguti, Giampiero; Petrella, Carla; Greco, Antonio; Ralli, Massimo; Minni, Antonio; Spaziani, Matteo; Isidori, Andrea M; Certo, Maria Grazia Di; Barbato, Christian; Putotto, Carolina; Fiore, Marco - 01a Articolo in rivista
paper: ENDOCRINE, METABOLIC & IMMUNE DISORDERS. DRUG TARGETS (Hilversum : Bentham Science Publishers) pp. 105-114 - issn: 2212-3873 - wos: WOS:000943752400011 (6) - scopus: 2-s2.0-85140654679 (7)
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
paper: SCHIZOPHRENIA BULLETIN OPEN (Cary NC: Oxford University Press) pp. 1-10 - issn: 2632-7899 - wos: (0) - scopus: 2-s2.0-85130703471 (5)
11573/1650039 - 2022 -
Hybrid single-stage repair of kommerell’s diverticulum in a right aortic arch in a patient with 22q11.2 deletion syndrome Chourda, E.; Putotto, C.; Versacci, P.; Saltarocchi, S.; D'abramo, M.; Tshomba, Y.; Tinelli, G.; Miraldi, F. - 01i Case report
paper: VASCULAR AND ENDOVASCULAR SURGERY (Westminster Publications Incorporated:708 Glen Cove Avenue:Glen Head, NY 11545:(516)759-0025, EMAIL: carolbrown@westminster.com, INTERNET: http://www.westministerpublications.com, Fax: (516)759-5524) pp. 595-601 - issn: 1538-5744 - wos: WOS:000787323800001 (0) - scopus: 2-s2.0-85129611255 (0)
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)
paper: HEART FAILURE CLINICS (Philadelphia : Saunders, c2005-) pp. 155-164 - issn: 1551-7136 - wos: WOS:000719585000015 (19) - scopus: 2-s2.0-85117920734 (27)
Delogu, Angelica Bibiana; Limongelli, Giuseppe; Versacci, Paolo; Adorisio, Rachele; Kaski, Juan Pablo; Blandino, Rita; Maiolo, Stella; Monda, Emanuele; Putotto, Carolina; De Rosa, Gabriella; Chatfield, Kathryn C; Gelb, Bruce D; Calcagni, Giulio - 01a Articolo in rivista
paper: AMERICAN JOURNAL OF MEDICAL GENETICS. PART C, SEMINARS IN MEDICAL GENETICS (Hoboken, NJ : Wiley-Liss, c2003) pp. - - issn: 1552-4868 - wos: WOS:000888446400001 (10) - scopus: 2-s2.0-85143440443 (10)
11573/1619107 - 2022 -
Serum prokineticin-2 in prepubertal and adult Klinefelter individuals Fiore, M.; Tarani, L.; Radicioni, A.; Spaziani, M.; Ferraguti, G.; Putotto, C.; Gabanella, F.; Maftei, D.; Lattanzi, R.; Minni, A.; Greco, A.; Tarani, F.; Petrella, C. - 01a Articolo in rivista
paper: CANADIAN JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY (NRC Research Press:National Research Council Canada, Ottawa Ontario K1A 0R6 Canada:(613)990-7873, (613)990-7873, (613)990-7873, (613)993-9084, (613)993-9084, EMAIL: eileen.evans-nantais@nrc-cnrc.gc.ca, INTERNET: http://www.researchpress.nrc.ca, Fax: (613)952-7656) pp. 151-157 - issn: 0008-4212 - wos: WOS:000751892200007 (10) - scopus: 2-s2.0-85124055684 (10)
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)
paper: HEART FAILURE CLINICS (Philadelphia : Saunders, c2005-) pp. 19-29 - issn: 1551-7136 - wos: WOS:000719585000004 (29) - scopus: 2-s2.0-85117832176 (31)
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
paper: 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 (5) - scopus: 2-s2.0-85129191379 (5)
11573/1672389 - 2022 -
Coexisting genetic findings in a cohort of patients with laboratory confirmation of 22q11.2 deletion
syndrome Pugnaloni, F.; Putotto, C.; Mastromoro, G.; Pulvirenti, F.; Maiolo, S.; Unolt, M.; Digilio, M. C.; Giovannetti, A.; Caputo, V.; Versacci, P.; Marino, B. - 04f Poster
conference: Italian Society of Paediatric Cardiology SICPED (Verona)
book: Atti del congresso SICPED - ()
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
paper: JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY. IN PRACTICE (Amsterdam [u.a.] : Elsevier) pp. - - issn: 2213-2198 - wos: WOS:000914945100001 (3) - scopus: 2-s2.0-85142845523 (3)
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)
paper: CHILDREN (Basel: MDPI AG, 2014-) pp. 1-14 - issn: 2227-9067 - wos: WOS:000817704200001 (9) - scopus: 2-s2.0-85131526222 (10)
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
paper: 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 (1)
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
paper: GENES (Basel : Molecular Diversity Preservation International) pp. 2334- - issn: 2073-4425 - wos: WOS:000902748800001 (1) - scopus: 2-s2.0-85144573205 (1)
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)
paper: GENES (Basel : Molecular Diversity Preservation International) pp. 1047- - issn: 2073-4425 - wos: WOS:000677373200001 (12) - scopus: 2-s2.0-85110670442 (14)
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
paper: 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 (6) - scopus: 2-s2.0-85122498681 (7)
11573/1571394 - 2021 -
Impaction of regurgitation jet on anterior mitral leaflet is associated with diastolic dysfunction in patients with bicuspid aortic valve and mild insufficiency: a cardiovascular magnetic resonance study Galea, N.; Pambianchi, G.; Cundari, G.; Sturla, F.; Marchitelli, L.; Putotto, C.; Versacci, P.; De Paulis, R.; Francone, M.; Catalano, C. - 01a Articolo in rivista
paper: THE INTERNATIONAL JOURNAL OF CARDIOVASCULAR IMAGING (London; Dordrecht; Boston: Springer
London; Dordrecht; Boston: Kluwer Academic Publishers
Oaklyn, NJ : Field & Wood Publishers) pp. - - issn: 1569-5794 - wos: WOS:000691063800001 (3) - scopus: 2-s2.0-85113688232 (3)
11573/1693745 - 2021 -
Impaction of Regurgitation Jet on Anterior Mitral Leaflet Causes Diastolic Dysfunction in Patients With Bicuspid Aortic Valve and Mild Insufficiency: A Cardiovascular Magnetic Resonance Study Galea, Nicola; Pambianchi, Giacomo; Cundari, Giulia; Sturla, Francesco; Marchitelli, Livia; Putotto, Carolina; Versacci, Paolo; De Paulis, Ruggero; Francone, Marco; Catalano, Carlo - 01a Articolo in rivista
paper: THE INTERNATIONAL JOURNAL OF CARDIOVASCULAR IMAGING (Boston ; Dordrecht : Kluwer Academic Publishers) pp. - - issn: 1875-8312 - wos: WOS:000691063800001 (3) - scopus: 2-s2.0-85113688232 (3)
11573/1556787 - 2021 -
Copy number variation analysis implicates novel pathways in patients with oculo-auriculo-vertebral-spectrum and congenital heart defects Guida, V.; Piceci Sparascio, F.; Bernardini, L.; Pancheri, F.; Melis, D.; Cocciadiferro, D.; Pagnoni, M.; Puzzo, M.; Goldoni, M.; Barone, C.; Hozhabri, H.; Putotto, C.; Giuffrida, M. G.; Briuglia, S.; Palumbo, O.; Bianca, S.; Stanzial, F.; Benedicenti, F.; Kariminejad, A.; Forzano, F.; Baghernajad Salehi, L.; Mattina, T.; Brancati, F.; Castori, M.; Carella, M.; Fadda, M. T.; Iannetti, G.; Dallapiccola, B.; Digilio, M. C.; Marino, B.; Tartaglia, M.; De Luca, A. - 01a Articolo in rivista
paper: 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. 1-12 - issn: 0009-9163 - wos: WOS:000653240400001 (4) - scopus: 2-s2.0-85106290806 (3)
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
paper: ANNALS OF PEDIATRIC CARDIOLOGY (Mumbai : Medknow Publications) pp. 250-251 - issn: 0974-2069 - wos: WOS:000649437900027 (0) - scopus: 2-s2.0-85105717679 (0)
11573/1618411 - 2021 -
Long-term outcome of a patient with Transcobalamin deficiency caused by the homozygous c.1115_1116delCA mutation in TCN2 gene. a case report Martino, F.; Magenta, A.; Troccoli, M. L.; Martino, E.; Torromeo, C.; Putotto, C.; Barilla, F. - 01i Case report
paper: THE ITALIAN JOURNAL OF PEDIATRICS (London: BioMed Central Ltd. 2008-
-Pacini Editore) pp. 1-6 - issn: 1720-8424 - wos: WOS:000626652500001 (2) - scopus: 2-s2.0-85102692278 (2)
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
paper: FRONTIERS IN PEDIATRICS (Lausanne : Frontiers Media S.A., 2013-) pp. 782779- - issn: 2296-2360 - wos: WOS:000721075400001 (0) - scopus: 2-s2.0-85119699868 (0)
11573/1427295 - 2020 -
Social cognition deficit and genetic vulnerability to schizophrenia in 22q11 deletion syndrome Frascarelli, M.; Padovani, G.; Buzzanca, A.; Accinni, T.; Carlone, L.; Ghezzi, F.; Lattanzi, Guido Maria; Fanella, M.; Putotto, C.; Di Bonaventura, C.; Girardi, N.; Pasquini, M.; Biondi, M.; Di Fabio, Fabio - 01a Articolo in rivista
paper: ANNALI DELL'ISTITUTO SUPERIORE DI SANITÀ (Latest publisher: Roma: Istituto Superiore di Sanità
Roma: Istituto poligrafico dello stato) pp. 107-113 - issn: 0021-2571 - wos: WOS:000537619500015 (7) - scopus: 2-s2.0-85082897017 (8)
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
paper: 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 (9)
11573/1401091 - 2020 -
Neuroinflammatory markers in the serum of prepubertal children with down syndrome Tarani, L.; Carito, V.; Ferraguti, G.; Petrella, C.; Greco, A.; Ralli, M.; Messina, M. P.; Rasio, D.; De Luca, E.; Putotto, C.; Versacci, P.; Ceccanti, M.; Fiore, M. - 01a Articolo in rivista
paper: JOURNAL OF IMMUNOLOGY RESEARCH (Cairo : Hindawi Publishing Corporation) pp. 1-10 - issn: 2314-8861 - wos: WOS:000524299900001 (21) - scopus: 2-s2.0-85083257531 (22)
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
paper: PLOS ONE (San Francisco, CA : Public Library of Science) pp. - - issn: 1932-6203 - wos: WOS:000462867000004 (10) - scopus: 2-s2.0-85063658968 (12)
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
paper: 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)
11573/1343159 - 2018 -
Partial atrioventricular septal defect in infancy: Don't we need to know more? Di Carlo, D.; Putotto, C.; Marino, B. - 01f Lettera, Nota
paper: 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)
11573/1325539 - 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
paper: JOURNAL OF RARE DISORDERS. DIAGNOSIS & THERAPY (Wilmington, Delaware: iMedPub, 2015-) pp. 1-7 - issn: 2380-7245 - wos: (0) - scopus: (0)
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
paper: 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)
11573/963752 - 2017 -
Factors that negatively affect the prognosis of pediatric community-acquired pneumonia in district hospital in Tanzania Caggiano, Serena; Ullmann, Nicola; De Vitis, Elisa; Trivelli, Marzia; Mariani, Chiara; Podagrosi, Maria; Ursitti, Fabiana; Bertolaso, Chiara; Putotto, Carolina; Unolt, Marta; Pietravalle, Andrea; Pansa, Paola; Mphayokulela, Kajoro; Lemmo, Maria Incoronata; Mkwambe, Michael; Kazaura, Joseph; Duse, Marzia; Nieddu, Francesco; Azzari, Chiara; Cutrera, Renato - 01a Articolo in rivista
paper: INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (Basel (Matthaeustrasse 11) : Molecular Diversity Preservation International MDPI) pp. - - issn: 1661-6596 - wos: WOS:000396253700152 (13) - scopus: 2-s2.0-85015269847 (17)
11573/1343161 - 2013 -
Double-outlet left ventricle with l-malposition of the great arteries and subpulmonary ventricular septal defect Putotto, C.; Unolt, M.; Marino, D. - 01b Commento, Erratum, Replica e simili
paper: 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. 1521-1521 - issn: 0172-0643 - wos: WOS:000321919400035 (1) - scopus: 2-s2.0-84880820447 (0)
11573/1343169 - 2013 -
Aortic arch interruption without ductus arteriosus and no ventricular septal defect Putotto, C.; Unolt, M.; Marino, D. - 01b Commento, Erratum, Replica e simili
paper: JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY (New York: Elsevier
Orlando, FL: Mosby Year Book) pp. 311-311 - issn: 0022-5223 - wos: WOS:000312386300061 (1) - scopus: 2-s2.0-84871247813 (2)
11573/1343171 - 2013 -
Smith-Lemli-Opitz syndrome, cardiac defects, and spleen anomalies Putotto, C.; Unolt, M.; Marino, D. - 01b Commento, Erratum, Replica e simili
paper: EUROPEAN JOURNAL OF MEDICAL GENETICS (AMSTERDAM, NETHERLANDS,: ELSEVIER SCIENCE BV) pp. 123-123 - issn: 1769-7212 - wos: WOS:000314627900010 (0) - scopus: 2-s2.0-84873170638 (0)
Putotto, C; Unolt, M; Caiaro, A; Marino Taussig De Bodonia, Bruno; Massaccesi, V; Digilio, Mc - 01g Articolo di rassegna (Review)
paper: 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
paper: 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)
11573/1343167 - 2013 -
Double-orifice left atrioventricular valve in patients with atrioventricular septal defect with and without down syndrome Unolt, M.; Putotto, C.; Marino, D. - 01b Commento, Erratum, Replica e simili
paper: ANNALS OF THORACIC SURGERY ([Boston etc.]: [Little Brown & Co. etc.]) pp. 1843-1844 - issn: 0003-4975 - wos: WOS:000318969500094 (1) - scopus: 2-s2.0-84876534760 (1)
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
paper: FRONTIERS IN PEDIATRICS (Lausanne : Frontiers Media S.A., 2013-) pp. 11- - issn: 2296-2360 - wos: WOS:000209895600011 (62) - scopus: 2-s2.0-84905174782 (78)
11573/1343163 - 2012 -
Atrioventricular septal defect prognosis for patients with down syndrome Unolt, M.; Putotto, C.; Marino, D. - 01b Commento, Erratum, Replica e simili
paper: 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. 1476-1476 - issn: 0172-0643 - wos: WOS:000311792000044 (2) - scopus: 2-s2.0-84878248607 (2)
11573/1343165 - 2012 -
Congenital heart disease, genetic syndromes, and major noncardiac malformations Unolt, M.; Putotto, C.; Marino, D. - 01b Commento, Erratum, Replica e simili
paper: 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. 1861-1861 - issn: 0340-6199 - wos: WOS:000311779700021 (1) - scopus: 2-s2.0-84879137745 (1)