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Volumn 17, Issue 5, 1999, Pages 859-864

Congenital long-QT syndrome: A case report illustrating diagnostic pitfalls

Author keywords

Jervell Lange Nielsen syndrome; Long QT syndrome; Torsade de pointes

Indexed keywords

ARTICLE; CARDIOVERSION; CASE REPORT; CHILD; DEFIBRILLATION; DIAGNOSTIC TEST; DISEASE COURSE; ELECTROCARDIOGRAPHY; GENE SEQUENCE; HEART ARRHYTHMIA; HUMAN; LONG QT SYNDROME; MALE; PRIORITY JOURNAL; SUDDEN DEATH; TORSADE DES POINTES;

EID: 0033199720     PISSN: 07364679     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0736-4679(99)00096-7     Document Type: Article
Times cited : (16)

References (13)
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  • 2
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  • 3
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    • The spectrum of symptoms and QT intervals in carriers of the gene for the long-QT syndrome
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  • 5
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    • Torsade de pointes and proarrhythmia
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  • 6
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    • Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval, and sudden death
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    • Jervell, A.1    Lange-Nielsen, F.2
  • 7
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    • Artimie cardiache rare dell'eta' pediatrica: II. Accessi sincopali per fibrillazione ventricolare parossitica
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    • Romano, C.1    Gemm, G.2    Pongiglione, R.3
  • 8
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    • A new familial cardiac syndrome in children
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  • 9
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    • Genetic hearing loss associated with miscellaneous disorders
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    • Gorlin R.J. Genetic hearing loss associated with miscellaneous disorders. Gorlin R.J., Toriello H.V., Cohen M.M. Hereditary hearing loss and its syndromes. 1st edn. 1995;418-419 Oxford University Press, New York.
    • (1995) Hereditary Hearing Loss and Its Syndromes 1st Edn. , pp. 418-419
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  • 10
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    • Pathology of the ear in the cardioauditory syndrome of Jervell and Lange-Nielsen
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  • 12
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    • Inner ear deficiencies induced by null mutations of the isk gene
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.