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BMC Medical Genetics|September 17, 2018
First evidence of maternally inherited mosaicism in TGFBR1 and subtle primary myocardial changes in Loeys-Dietz syndrome: a case reportAnwar Baban, Monia Magliozzi, Bart Loeys, et al.
Pediatric Cardiology|June 28, 2018
Bradyarrhythmias in Repaired Atrioventricular Septal Defects: Single-Center Experience Based on 34 Years of Follow-Up of 522 PatientsCorrado Di Mambro, Camilla Calvieri, Massimo Stefano Silvetti, et al.
The Journal of Thoracic and Cardiovascular Surgery|November 14, 2009
Dextrocardia in patients with Poland syndrome: phenotypic characterization provides insight into the pathogenesisMichele Torre, Anwar Baban, Anna Buluggiu, et al.
Cardiology in the Young|September 13, 2024
The role of Italian pre-participation screening in early detection of cardiomyopathies: what is the meaning of T wave inversion in young athletes?Eliana Tranchita, Giulia Cafiero, Ugo Giordano, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|December 18, 2020
Progressive involvement of cardiac conduction system in paediatric patients with Kearns-Sayre syndrome: how to predict occurrence of complete heart block and sudden cardiac death?Corrado Di Mambro, Pietro Paolo Tamborrino, Massimo Stefano Silvetti, et al.
Pediatric Cardiology|April 10, 2021
Deciphering Genetic Variants of Warfarin Metabolism in Children With Ventricular Assist DevicesAnwar Baban, Francesca G Iodice, Arianna Di Molfetta, et al.
BMC Medical Genetics|June 3, 2014
Exome sequencing identifies a novel mutation in PIK3R1 as the cause of SHORT syndromeClea Bárcena, Víctor Quesada, Annachiara De Sandre-Giovannoli, et al.
American Journal of Medical Genetics. Part A|September 9, 2017
Congenital heart defects in molecularly proven Kabuki syndrome patientsMaria Cristina Digilio, Maria Gnazzo, Francesca Lepri, et al.
International Journal of Cardiology|January 9, 2022
Arrhythmogenic cardiomyopathy in children according to "Padua criteria": Single pediatric center experienceMarianna Cicenia, Nicoletta Cantarutti, Rachele Adorisio, et al.
American Journal of Medical Genetics. Part A|August 2, 2019
SOS1 mutations in Noonan syndrome: Cardiomyopathies and not only congenital heart defects! Report of six patients including two novel variants and literature reviewAnwar Baban, Nicole Olivini, Francesca Romana Lepri, et al.
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