Genetic predisposition and cellular basis for ischemia-induced ST-segment changes and arrhythmias

Journal of Electrocardiology

Volumn 40, Issue 6 SUPPL. 1, 2007, Pages

  Hu, Dan ^a   Viskin, Sami ^b   Oliva, Antonio ^a,c   Cordeiro, Jonathan M ^a   Guerchicoff, Alejandra ^a   Pollevick, Guido D ^a   Antzelevitch, Charles ^a  

^a MASONIC MEDICAL RESEARCH LABORATORY   (United States)

^b TEL AVIV SOURASKY MEDICAL CENTER   (Israel)

^c CATHOLIC UNIVERSITY   (Italy)

Author keywords

Arrhythmia; Fibrillation; Ischemia; Sudden cardiac death; Ventricular tachycardia

Indexed keywords

DELAYED RECTIFIER POTASSIUM CHANNEL; SODIUM CHANNEL;

ADULT; AGED; ALLELE; ALPHA CHAIN; ARRHYTHMOGENESIS; ARTICLE; BRUGADA SYNDROME; CLINICAL ARTICLE; COHORT ANALYSIS; DISEASE ASSOCIATION; DISEASE SEVERITY; EXTRASYSTOLE; FAMILY HISTORY; GENE; GENE EXPRESSION; GENE MUTATION; GENETIC POLYMORPHISM; GENETIC PREDISPOSITION; GENETIC SCREENING; HEART ARRHYTHMIA; HEART MUSCLE ISCHEMIA; HEART VENTRICLE FIBRILLATION; HUMAN; KCNH2 GENE; MISSENSE MUTATION; POTASSIUM CURRENT; PRIORITY JOURNAL; QT PROLONGATION; REENTRY ARRHYTHMIA; SCN5A GENE; ST SEGMENT; SUDDEN DEATH; TORSADE DES POINTES;

ARRHYTHMIAS, CARDIAC; DNA MUTATIONAL ANALYSIS; FEMALE; GENETIC MARKERS; GENETIC PREDISPOSITION TO DISEASE; HUMANS; LONG QT SYNDROME; MALE; MIDDLE AGED; MUSCLE PROTEINS; MUTATION; MYOCARDIAL ISCHEMIA; POLYMORPHISM, SINGLE NUCLEOTIDE; SODIUM CHANNELS;

EID: 35748932349     PISSN: 00220736     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jelectrocard.2007.05.019     Document Type: Article

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