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A mutation in the beta 3 subunit of the cardiac sodium channel associated with Brugada ECG phenotype

artículo científico publicado en 2009

An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing

artículo científico publicado en 2009

Analysis of biomarkers for risk of acute kidney injury after primary angioplasty for acute ST-segment elevation myocardial infarction: results of the HORIZONS-AMI trial

artículo científico publicado en 2014

Complementary prognostic utility of myocardial blush grade and ST-segment resolution after primary percutaneous coronary intervention: analysis from the HORIZONS-AMI trial

artículo científico publicado en 2013

Cryptic 5' splice site activation in SCN5A associated with Brugada syndrome

artículo científico publicado en 2004

Dual variation in SCN5A and CACNB2b underlies the development of cardiac conduction disease without Brugada syndrome.

artículo científico publicado en 2009

Gain of function in IKs secondary to a mutation in KCNE5 associated with atrial fibrillation

artículo científico publicado en 2008

Impact of delay to reperfusion on reperfusion success, infarct size, and clinical outcomes in patients with ST-segment elevation myocardial infarction: the INFUSE-AMI Trial (INFUSE-Anterior Myocardial Infarction).

artículo científico publicado en 2014

Impact of pre-procedural cardiopulmonary instability in patients with acute myocardial infarction undergoing primary percutaneous coronary intervention (from the Harmonizing Outcomes With Revascularization and Stents in Acute Myocardial Infarction T

artículo científico publicado en 2014

Loss-of-function mutations in the cardiac calcium channel underlie a new clinical entity characterized by ST-segment elevation, short QT intervals, and sudden cardiac death

artículo científico publicado en 2007

Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death.

artículo científico publicado en 2010

Novel mutation in the SCN5A gene associated with arrhythmic storm development during acute myocardial infarction

artículo científico publicado en 2007

Sudden death associated with short-QT syndrome linked to mutations in HERG.

artículo científico publicado en 2003

Value of electrocardiographic parameters and ajmaline test in the diagnosis of Brugada syndrome caused by SCN5A mutations

artículo científico publicado en 2004

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