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)
11573/1441084 - 2020 -
The global emergency of novel coronavirus (SARS-CoV-2). An update of the current status and forecasting Hozhabri, Hossein; Piceci Sparascio, Francesca; Sohrabi, Hamidreza; Mousavifar, Leila; Roy, René; Scribano, Daniela; De Luca, Alessandro; Ambrosi Sacconi Rosati, Cecilia; Sarsharjeryandeh, Meysam - 01g Articolo di rassegna (Review)
paper: INTERNATIONAL JOURNAL OF ENVIRONMENTAL RESEARCH AND PUBLIC HEALTH (Basel: MDPI 2003-) pp. 1-34 - issn: 1660-4601 - wos: WOS:000566391600001 (36) - scopus: 2-s2.0-85089262051 (44)
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
paper: GENES (Basel : Molecular Diversity Preservation International) pp. - - issn: 2073-4425 - wos: WOS:000487954700065 (15) - scopus: 2-s2.0-85071740488 (22)
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
paper: 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 (16) - scopus: 2-s2.0-85051056677 (18)