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Giulio Calcagni

Showing results (51-60 of 66) with videos related to

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American Journal of Medical Genetics. Part A|April 18, 2018
Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiersMarta Unolt, Paolo Versacci, Silvia Anaclerio, et al.
American Journal of Medical Genetics. Part A|April 23, 2020
Differences in morbidity and mortality in Down syndrome are related to the type of congenital heart defectAnwar Baban, Nicole Olivini, Nicoletta Cantarutti, et al.
Plos One|April 2, 2019
Left pulmonary artery in 22q11.2 deletion syndrome. Echocardiographic evaluation in patients without cardiac defects and role of Tbx1 in miceGioia Mastromoro, Giulio Calcagni, Paolo Versacci, et al.
Circulation. Genomic and Precision Medicine|May 18, 2023
Natural History of Hypertrophic Cardiomyopathy in Noonan Syndrome With Multiple LentiginesEmanuele Monda, Aaron Prosnitz, Rossella Aiello, et al.
American Journal of Medical Genetics. Part A|December 31, 2021
Congenital heart defects in molecularly confirmed KBG syndrome patientsMaria Cristina Digilio, Giulio Calcagni, Maria Gnazzo, et al.
Journal of Clinical Medicine|February 15, 2022
Syndromic and Non-Syndromic Patients with Repaired Tetralogy of Fallot: Does It Affect the Long-Term Outcome?Giulio Calcagni, Camilla Calvieri, Anwar Baban, et al.
Diagnostics (Basel, Switzerland)|March 27, 2024
Congenital Heart Defects in Patients with Molecularly Confirmed Sotos SyndromeGiulio Calcagni, Federica Ferrigno, Alessio Franceschini, et al.
Human Mutation|July 15, 2018
Heterozygous missense mutations in NFATC1 are associated with atrioventricular septal defectRosangela Ferese, Monica Bonetti, Federica Consoli, et al.
European Heart Journal. Digital Health|July 14, 2026
Rational and design of the digital diagnosis of cardiac sounds in paediatric patients (DI_SOUND) studyGabriele Egidy Assenza, Alessandro Colombo, Vittoria Mastromarino, et al.
European Journal of Human Genetics : EJHG|June 1, 2024
Defining the variant-phenotype correlation in patients affected by Noonan syndrome with the RAF1:c.770C>T p.(Ser257Leu) variantAndrea Gazzin, Federico Fornari, Marcello Niceta, et al.
Pageof 7

Showing results (51-60 of 66) with videos related to

Sort By:
Pageof 7
American Journal of Medical Genetics. Part A|April 18, 2018
Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiersMarta Unolt, Paolo Versacci, Silvia Anaclerio, et al.
American Journal of Medical Genetics. Part A|April 23, 2020
Differences in morbidity and mortality in Down syndrome are related to the type of congenital heart defectAnwar Baban, Nicole Olivini, Nicoletta Cantarutti, et al.
Plos One|April 2, 2019
Left pulmonary artery in 22q11.2 deletion syndrome. Echocardiographic evaluation in patients without cardiac defects and role of Tbx1 in miceGioia Mastromoro, Giulio Calcagni, Paolo Versacci, et al.
Circulation. Genomic and Precision Medicine|May 18, 2023
Natural History of Hypertrophic Cardiomyopathy in Noonan Syndrome With Multiple LentiginesEmanuele Monda, Aaron Prosnitz, Rossella Aiello, et al.
American Journal of Medical Genetics. Part A|December 31, 2021
Congenital heart defects in molecularly confirmed KBG syndrome patientsMaria Cristina Digilio, Giulio Calcagni, Maria Gnazzo, et al.
Journal of Clinical Medicine|February 15, 2022
Syndromic and Non-Syndromic Patients with Repaired Tetralogy of Fallot: Does It Affect the Long-Term Outcome?Giulio Calcagni, Camilla Calvieri, Anwar Baban, et al.
Diagnostics (Basel, Switzerland)|March 27, 2024
Congenital Heart Defects in Patients with Molecularly Confirmed Sotos SyndromeGiulio Calcagni, Federica Ferrigno, Alessio Franceschini, et al.
Human Mutation|July 15, 2018
Heterozygous missense mutations in NFATC1 are associated with atrioventricular septal defectRosangela Ferese, Monica Bonetti, Federica Consoli, et al.
European Heart Journal. Digital Health|July 14, 2026
Rational and design of the digital diagnosis of cardiac sounds in paediatric patients (DI_SOUND) studyGabriele Egidy Assenza, Alessandro Colombo, Vittoria Mastromarino, et al.
European Journal of Human Genetics : EJHG|June 1, 2024
Defining the variant-phenotype correlation in patients affected by Noonan syndrome with the RAF1:c.770C>T p.(Ser257Leu) variantAndrea Gazzin, Federico Fornari, Marcello Niceta, et al.
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