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Journal of Geriatric Cardiology : JGC|October 30, 2015
Serum uric acid as a prognostic marker in the setting of advanced vascular disease: a prospective study in the elderlyGiuseppe Di Stolfo, Sandra Mastroianno, Domenico Rosario Potenza, et al.Obesity (Silver Spring, Md.)|May 15, 2007
Heterogeneous effect of peroxisome proliferator-activated receptor gamma2 Ala12 variant on type 2 diabetes riskOrnella Ludovico, Fabio Pellegrini, Rosa Di Paola, et al.Molecular Genetics & Genomic Medicine|July 27, 2019
Long QT syndrome in chromosome 7q35q36.3 deletion involving KCNH2 gene: Warning for chlorpheniramine prescriptionGiuseppe Di Stolfo, Maria Accadia, Sandra Mastroianno, et al.Annals of Noninvasive Electrocardiology : the Official Journal of the International Society for Holter and Noninvasive Electrocardiology, Inc|September 17, 2019
Double missense mutations in cardiac myosin-binding protein C and myopalladin genes: A case report with diffuse coronary disease, complete atrioventricular block, and progression to dilated cardiomyopathySandra Mastroianno, Pietro Palumbo, Stefano Castellana, et al.Journal of Clinical Medicine|February 13, 2025
Role of C-Reactive Protein as a Predictor of Early Revascularization and Mortality in Advanced Peripheral Arterial DiseaseGiuseppe Di Stolfo, Mario Mastroianno, Michele Antonio Pacilli, et al.Frontiers in Cardiovascular Medicine|June 7, 2021
Phenotypic Variability of a Pathogenic PKP2 Mutation in an Italian Family Affected by Arrhythmogenic Cardiomyopathy and Juvenile Sudden Death: Considerations From Molecular Autopsy to Sport RestrictionMaria Pia Leone, Pietro Palumbo, Johan Saenen, et al.Journal of Electrocardiology|September 5, 2018
Sudden cardiac death in J wave syndrome with short QT associated to a novel mutation in Nav 1.8 coding gene SCN10A: First case report for a possible pharmacogenomic roleGiuseppe Di Stolfo, Pietro Palumbo, Stefano Castellana, et al.Endocrine|June 17, 2011
Coexistence of multiple endocrine neoplasia type 1 and type 2 in a large Italian familySandra Mastroianno, Massimo Torlontano, Alfredo Scillitani, et al.Plos One|March 2, 2017
Role of the APOE polymorphism in carotid and lower limb revascularization: A prospective study from Southern ItalySandra Mastroianno, Giuseppe Di Stolfo, Davide Seripa, et al.Journal of Electrocardiology|February 5, 2019
Sudden death in mild hypertrophic cardiomyopathy with compound DSG2/DSC2/MYH6 mutations: Revisiting phenotype after genetic assessment in a master runner athleteStefano Castellana, Sandra Mastroianno, Pietro Palumbo, et al.Pageof 3