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Author/Creator Calcagni, Giulio

1. Atypical cardiac defects in patients with RASopathies: Updated data on CARNET study. Issue 10 (18th June 2020)

Authors:
Calcagni, Giulio; Gagliostro, Giulia; Limongelli, Giuseppe; Unolt, Marta; De Luca, Enrica; Digilio, Maria C.; Baban, Anwar; Albanese, Sonia B.; Ferrero, Giovanni B.; Baldassarre, Giuseppina; Agnoletti, Gabriella; Banaudi, Elena; Marek, Jan; Kaski, Juan P.; Tuo, Giulia; Marasini, Maurizio; Cairell...
Other Names:
Watanabe Michiko guestEditor.
Journal:
Birth defects research
Issue:
Volume 112:Issue 10(2020)
Page Start:
725
Record Type:
Journal Article
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2. Cardiac defects, morbidity and mortality in patients affected by RASopathies. CARNET study results. (15th October 2017)

Authors:
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; ...
Journal:
International journal of cardiology
Issue:
Volume 245(2017)
Page Start:
92
Record Type:
Journal Article
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3. Congenital heart defects in molecularly confirmed KBG syndrome patients. Issue 4 (31st December 2021)

Authors:
Digilio, Maria Cristina; Calcagni, Giulio; Gnazzo, Maria; Versacci, Paolo; Dentici, Maria Lisa; Capolino, Rossella; Sinibaldi, Lorenzo; Baban, Anwar; Putotto, Carolina; Alfieri, Paolo; Unolt, Marta; Lepri, Francesca R.; Alesi, Viola; Genovese, Silvia; Novelli, Antonio; Marino, Bruno; Dallapiccola...
Journal:
American journal of medical genetics
Issue:
Volume 188:Issue 4(2022)
Page Start:
1149
Record Type:
Journal Article
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5. Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well‐established knowledge to new frontiers. Issue 10 (16th April 2018)

Authors:
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
Other Names:
McDonald‐McGinn Donna M. guestEditor.
Journal:
American journal of medical genetics
Issue:
Volume 176:Issue 10(2018)
Page Start:
2087
Record Type:
Journal Article
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7. Cover Image, Volume 39, Issue 10. Issue 10 (19th September 2018)

Authors:
Ferese, Rosangela; Bonetti, Monica; Consoli, Federica; Guida, Valentina; Sarkozy, Anna; Lepri, Francesca Romana; Versacci, Paolo; Gambardella, Stefano; Calcagni, Giulio; Margiotti, Katia; Piceci Sparascio, Francesca; Hozhabri, Hossein; Mazza, Tommaso; Digilio, Maria Cristina; Dallapiccola, Bruno;...
Journal:
Human mutation
Issue:
Volume 39:Issue 10(2018)
Page Start:
i
Record Type:
Journal Article
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8. Crossed pulmonary arteries: An underestimated cardiovascular variant with a strong association with genetic syndromes—A report of 74 cases with systematic review of the literature. Issue 8 (2nd May 2022)

Authors:
Mastromoro, Gioia; Calcagni, Giulio; Vignaroli, Walter; Anaclerio, Silvia; Pugnaloni, Flaminia; Rinelli, Gabriele; Secinaro, Aurelio; Bordonaro, Veronica; Putotto, Carolina; Unolt, Marta; Digilio, Maria Cristina; Marino, Bruno; Versacci, Paolo
Journal:
American journal of medical genetics
Issue:
Volume 188:Issue 8(2022)
Page Start:
2351
Record Type:
Journal Article
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9. Differences in morbidity and mortality in Down syndrome are related to the type of congenital heart defect. Issue 6 (22nd April 2020)

Authors:
Baban, Anwar; Olivini, Nicole; Cantarutti, Nicoletta; Calì, Federica; Vitello, Carmen; Valentini, Diletta; Adorisio, Rachele; Calcagni, Giulio; Alesi, Viola; Di Mambro, Corrado; Villani, Alberto; Dallapiccola, Bruno; Digilio, Maria Cristina; Marino, Bruno; Carotti, Adriano; Drago, Fabrizio
Journal:
American journal of medical genetics
Issue:
Volume 182:Issue 6(2020)
Page Start:
1342
Record Type:
Journal Article
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10. Heterozygous missense mutations in NFATC1 are associated with atrioventricular septal defect. Issue 10 (30th July 2018)

Authors:
Ferese, Rosangela; Bonetti, Monica; Consoli, Federica; Guida, Valentina; Sarkozy, Anna; Lepri, Francesca Romana; Versacci, Paolo; Gambardella, Stefano; Calcagni, Giulio; Margiotti, Katia; Piceci Sparascio, Francesca; Hozhabri, Hossein; Mazza, Tommaso; Digilio, Maria Cristina; Dallapiccola, Bruno;...
Journal:
Human mutation
Issue:
Volume 39:Issue 10(2018)
Page Start:
1428
Record Type:
Journal Article
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