Ion channels and beating heart: the players and the music

by Charles Antzelevitch, Giuseppe Limongelli, Lia Crotti
Published 2011-12-01

Echocardiography in Fabry disease

by Markus Niemann, Frank Weidemann
Published 2013-06-01

Measurement of troponin in cardiomyopathies

by Andrew Connelly, Iain N. Findlay, Caroline J. Coats
Published 2016-12-01

Ranolazine treatment for refractory angina in a patient with Hutchinson-Gilford progeria syndrome and end stage aortic stenosis

by Giuseppe Limongelli, Emanuele Monda, Giovanbattista Capozzi, Martina Caiazza, Maria Giovanna Russo
Published 2020-01-01

High-density lipoproteincholesterol, reverse cholesterol transport, and cardiovascular risk: a tale of genetics?

by Giovanni Cimmino, Chiara D’Amico, Giovanni Ciccarelli, Marco Golino, Alberto Morello, Saverio D’Elia, Valeria Marchese, Paolo Golino
Published 2013-10-01

Phenotypic spectrum of mutations in cardiolaminopathies

by Ali J. Marian
Published 2011-07-01

Risk stratification in hypertrophic cardiomyopathy: Time to think about the electrocardiogram

by Jonathan R. Skinner
Published 2019-04-01

Long QT syndrome: from genetic basis to treatment

by Lia Crotti, Peter J. Schwartz, Federica Dagradi
Published 2011-12-01

J wave syndromes as a cause of sudden arrhythmic death

by Charles Antzelevitch
Published 2013-06-01

Myocardial deformation imaging and rare cardiomyopathies with hypertrophic phenotype: a review focused on Fabry disease, Friedreich ataxia and amyloidosis

by Bahaa Fadel, Luca Baldini, Valeria Pergola, Ziad Al Bulbul, Giovanni Di Salvo
Published 2013-06-01

Brugada syndrome

by Rachel Bastiaenen, Elijah R. Behr
Published 2011-12-01

Patent ductus arteriosus and pulmonary artery aneurism in a child affected by Loeys-Dietz syndrome

by Marcello Marcì
Published 2015-10-01

Pathogenesis of Takotsubo syndrome

by Daniele Masarone, Valeria Maddaloni, Marta Rubino, Fiorella Fratta, Annapaola Cirillo, Ludovica Spinelli Barrile, Roberta Pacileo, Adelaide Fusco, Guido Coppola, Francesca Pisacane, Paolo Calabrò, Raffaele Calabrò, Edoardo Bossone, Maria Giovanna Russo, Giuseppe Pacileo
Published 2017-01-01

Inherited interstitial deletion of 3p22.3—p23 involving <em>GPD1L</em> gene

by Hoang H. Nguyen, Krishna Kishore Umapathi, Richard Dineen, Raymond Morales, Mindy H. Li
Published 2020-09-01

Persistent left superior vena cava: an overlooked feature of CHARGE syndrome?

by Paula Goldenberg, Amy Shikany, Ashley Parrott, Stephanie M. Ware, Robert B. Hinton
Published 2015-12-01

Bicuspid aortic valve associated aortopathy: a genetic disease?

by Ciro Bancone, Marisa De Feo, Alessandro Della Corte
Published 2015-02-01

Arrhythmogenic right ventricular cardiomyopathy: From pathophysiology to diagnosis and advances in management

by Rachel Bastiaenen, Marc W. Deyell, Andrew D. Krahn
Published 2017-12-01

Restrictive cardiomyopathy and hypertrophic cardiomyopathy overlap: the importance of the phenotype

by Juan Pablo Kaski, Elena Biagini, Massimo Lorenzini, Claudio Rapezzi, Perry Elliott
Published 2012-10-01

An Unusual Cause of Right Heart Failure

by Paul Hill
Published 2019-06-01

Imaging in Rare Disease: a roadmap for diagnosis

by Giovanni Di Salvo, Giuseppe Limongelli
Published 2013-12-01