SCOPUS 정보 검색 플랫폼

Volumn 95, Issue 5, 2005, Pages 700-702

Unusual clinical presentation in a family with catecholaminergic polymorphic ventricular tachycardia due to a G14876A ryanodine receptor gene mutation

(5) Allouis, Marie a Probst, Vincent a,b Jaafar, Philippe a Schott, Jean Jacques a Le Marec, Hervé a

a L INSTITUT DU THORAX (France)

b NANTES UNIVERSITY HOSPITAL (France)

Author keywords

[No Author keywords available]

Indexed keywords

BETA ADRENERGIC RECEPTOR BLOCKING AGENT; DIPHEMANIL METHYLSULFATE; RYANODINE 2 RECEPTOR; RYANODINE RECEPTOR; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; ARTICLE; CATECHOLAMINERGIC SYSTEM; CHILD; CLINICAL FEATURE; CONTROLLED STUDY; DEFIBRILLATION; EXERCISE TEST; FAMILY; FEMALE; GENE MUTATION; HEART ARREST; HEART ARRHYTHMIA; HEART VENTRICLE TACHYCARDIA; HETEROZYGOTE; HUMAN; LONG QT SYNDROME; MALE; PRIORITY JOURNAL; RESUSCITATION; SLEEP; SUDDEN DEATH; SYMPTOMATOLOGY;

EID: 13844297632 PISSN: 00029149 EISSN: None Source Type: Journal
DOI: 10.1016/j.amjcard.2004.10.057 Document Type: Article

Times cited : (27)

References (8)

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