Congenital long QT syndrome;Syndrome du QT long congenital

Presse Medicale

Volumn 27, Issue 21, 1998, Pages 1029-1033

  Lupoglazoff, J M ^a   Denjoy, I ^b   Neyroud, N ^c   Guicheney, P ^c   Casasoprana, A ^a   Coumel, Ph ^b  

^a HÔPITAL ROBERT DEBRÉ   (France)

^b HÔPITAL LARIBOISIÈRE   (France)

^c PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

AUTOSOMAL INHERITANCE; CLINICAL FEATURE; DISEASE ASSOCIATION; ELECTROCARDIOGRAM; GENETIC ANALYSIS; HUMAN; LONG QT SYNDROME; MASS SCREENING; PATIENT MONITORING; PROGNOSIS; REVIEW; ELECTROCARDIOGRAPHY; FEMALE; GENETICS; GENOTYPE; HEARING IMPAIRMENT; MALE; PHENOTYPE; TORSADE DES POINTES;

BETA ADRENERGIC RECEPTOR BLOCKING AGENT;

ADRENERGIC BETA-ANTAGONISTS; DEAFNESS; ELECTROCARDIOGRAPHY, AMBULATORY; FEMALE; GENOTYPE; HUMANS; LONG QT SYNDROME; MALE; PHENOTYPE; PROGNOSIS; TORSADES DE POINTES;

EID: 0032513948     PISSN: 07554982     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

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