Filtros de búsqueda

Lista de obras de Charles I Berul

A molecular pathway including Id2, Tbx5, and Nkx2-5 required for cardiac conduction system development

scientific journal article

Calsequestrin 2 (CASQ2) mutations increase expression of calreticulin and ryanodine receptors, causing catecholaminergic polymorphic ventricular tachycardia

artículo científico publicado en 2007

Ectopic atrial rhythm is a preablation predictor of atrioventricular nodal reentrant tachycardia in children

artículo científico publicado en 2008

Electrophysiologic characterization and postnatal development of ventricular pre-excitation in a mouse model of cardiac hypertrophy and Wolff-Parkinson-White syndrome

artículo científico publicado en 2003

HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA).

artículo científico

HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies: this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA).

artículo científico publicado en 2011

Heart Rhythm Society/Pediatric and Congenital Electrophysiology Society Clinical Competency Statement: training pathways for implantation of cardioverter-defibrillators and cardiac resynchronization therapy devices in pediatric and congenital heart

artículo científico publicado en 2008

Increased alpha2 subunit-associated AMPK activity and PRKAG2 cardiomyopathy

artículo científico publicado en 2005

Indications and techniques of pediatric cardiac pacing

artículo científico publicado en 2003

Lamin A/C haploinsufficiency causes dilated cardiomyopathy and apoptosis-triggered cardiac conduction system disease.

artículo científico publicado en 2007

Reversibility of PRKAG2 glycogen-storage cardiomyopathy and electrophysiological manifestations

artículo científico publicado en 2007

Review of the registry's fourth year, incorporating lead data and pediatric ICD procedures, and use as a national performance measure.

artículo científico publicado en 2010

Somatic events modify hypertrophic cardiomyopathy pathology and link hypertrophy to arrhythmia

artículo científico publicado en 2005

The National ICD Registry Report: version 2.1 including leads and pediatrics for years 2010 and 2011.

artículo científico publicado en 2013

Transgenic mice overexpressing mutant PRKAG2 define the cause of Wolff-Parkinson-White syndrome in glycogen storage cardiomyopathy.

artículo científico publicado en 2003