Carnitine deficiency induces a short QT syndrome

Heart Rhythm

Volumn 13, Issue 1, 2016, Pages 165-174

  Roussel, Julien ^a   Labarthe, François ^b   Thireau, Jerome ^a   Ferro, Fabio ^a,b   Farah, Charlotte ^a   Roy, Jerome ^a   Horiuchi, Masahisa ^c   Tardieu, Martine ^b   Lefort, Bruno ^b   François Benoist, Jean ^d   Lacampagne, Alain ^a   Richard, Sylvain ^a   Fauconnier, Jeremy ^a   Babuty, Dominique ^b   Le Guennec, Jean Yves ^a  

^a UNIV MONTPELLIER   (France)

^b UNIVERSITÉ DE TOURS   (France)

^c KAGOSHIMA UNIVERSITY   (Japan)

^d HÔPITAL ROBERT DEBRÉ   (France)

Author keywords

Carnitine deficiency; Electrophysiological remodeling; Short QT syndrome; Sudden death; Ventricular arrhythmias

Indexed keywords

ACYLCARNITINE; CARBOXYLIC ACID; CARNITINE; MELDONIUM;

ADOLESCENT; ADULT; AMINO ACID BLOOD LEVEL; AMINO ACID SUBSTITUTION; ANGIOCARDIOGRAPHY; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CARNITINE DEFICIENCY; CASE REPORT; CELL ULTRASTRUCTURE; CHILD; COMPUTER PROGRAM; CONGESTIVE CARDIOMYOPATHY; CONTROLLED STUDY; DEFIBRILLATOR; DISEASE ASSOCIATION; ECHOCARDIOGRAPHY; ELECTROCARDIOGRAPHY MONITORING; EXON; FEMALE; GENE; GENE MUTATION; GENOTYPE; HEART ARRHYTHMIA; HEART FAILURE; HEART MITOCHONDRION; HEART VENTRICLE EXTRASYSTOLE; HEART VENTRICLE FIBRILLATION; HEART VENTRICLE HYPERTROPHY; HEART VENTRICLE REMODELING; HEART VENTRICLE TACHYCARDIA; HEPATOMEGALY; HETEROZYGOTE; HOLTER MONITORING; HUMAN; HYPOGLYCEMIA; INFANT; MALE; MISSENSE MUTATION; MOUSE; MUSCLE ATROPHY; NONHUMAN; PRESCHOOL CHILD; PRIORITY JOURNAL; QT INTERVAL; QTC INTERVAL; SCHOOL CHILD; SHORT QT SYNDROME; SLC22A5 GENE; STOP CODON; T WAVE; TANDEM MASS SPECTROMETRY; ANIMAL; ARRHYTHMIAS, CARDIAC; BLOOD; C57BL MOUSE; CARDIOMYOPATHIES; COMPLICATION; DEFICIENCY; DOPPLER ECHOCARDIOGRAPHY; ELECTROCARDIOGRAPHY; GENETICS; HEART FUNCTION TEST; HYPERAMMONEMIA; METABOLISM; MUSCULAR DISEASES; PATHOLOGY; PATHOPHYSIOLOGY; PROCEDURES; TREATMENT OUTCOME;

ADULT; ANIMALS; ARRHYTHMIAS, CARDIAC; CARDIOMYOPATHIES; CARNITINE; CHILD, PRESCHOOL; ECHOCARDIOGRAPHY, DOPPLER; ELECTROCARDIOGRAPHY; ELECTROPHYSIOLOGIC TECHNIQUES, CARDIAC; FEMALE; HUMANS; HYPERAMMONEMIA; INFANT; MALE; MICE; MICE, INBRED C57BL; MITOCHONDRIA, HEART; MUSCULAR DISEASES; TREATMENT OUTCOME;

EID: 84955509462     PISSN: 15475271     EISSN: 15563871     Source Type: Journal    
DOI: 10.1016/j.hrthm.2015.07.027     Document Type: Article

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