Literature DB >> 14255231

CONGENITAL CARDIAC ARRHYTHMIA.

C ROMANO.   

Abstract

Entities:  

Keywords:  CONVULSIONS; DEAF-MUTISM; DIAGNOSIS, DIFFERENTIAL; ELECTROCARDIOGRAPHY; HEART DEFECTS, CONGENITAL; INFANT; SYNCOPE; VENTRICULAR FIBRILLATION

Mesh：

Year:  1965        PMID： 14255231     DOI： 10.1016/s0140-6736(65)91761-7

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  18 in total

Review 1.  HERG potassium channel regulation by the N-terminal eag domain.

Authors:  Ahleah S Gustina; Matthew C Trudeau
Journal:  Cell Signal       Date:  2012-04-13       Impact factor: 4.315

2.  Properties of KvLQT1 K+ channel mutations in Romano-Ward and Jervell and Lange-Nielsen inherited cardiac arrhythmias.

Authors:  C Chouabe; N Neyroud; P Guicheney; M Lazdunski; G Romey; J Barhanin
Journal:  EMBO J       Date:  1997-09-01       Impact factor: 11.598

3.  Mutational and phenotypic spectra of KCNE1 deficiency in Jervell and Lange-Nielsen Syndrome and Romano-Ward Syndrome.

Authors:  Rabia Faridi; Risa Tona; Alessandra Brofferio; Michael Hoa; Rafal Olszewski; Isabelle Schrauwen; Muhammad Z K Assir; Akhtar A Bandesha; Asma A Khan; Atteeq U Rehman; Carmen Brewer; Wasim Ahmed; Suzanne M Leal; Sheikh Riazuddin; Steven E Boyden; Thomas B Friedman
Journal:  Hum Mutat       Date:  2018-12-12       Impact factor: 4.878

4.  Classification of the long-QT syndrome based on discriminant analysis of T-wave morphology.

Authors:  J J Struijk; J K Kanters; M P Andersen; T Hardahl; C Graff; M Christiansen; E Toft
Journal:  Med Biol Eng Comput       Date:  2006-06-03       Impact factor: 2.602

5.  A family with heritable electrocardiographic QT-prolongation.

Authors:  P J van der Straaten; C L Bruins
Journal:  J Med Genet       Date:  1973-06       Impact factor: 6.318

6.  Linkage of the long QT syndrome to the short arm of chromosome 11: use of five highly polymorphic markers towards more detailed localization of the mutant gene.

Authors:  K Kainulainen; H Swan; H Miettinen; M Viitasalo; L Rovamo; L Toivonen; K Kontula
Journal:  Hum Genet       Date:  1995-10       Impact factor: 4.132

7.  Study of left and right ventricular function in Romano-Ward syndrome.

Authors:  S J Cross; J C Dean; H S Lee; M Y Norton; N T Evans; F Smith; K Jennings; S Walton
Journal:  Br Heart J       Date:  1993-09

8.  Analysis of HLA and disease susceptibility: chromosome 6 genes and sex influence long-QT phenotype.

Authors:  L R Weitkamp; A J Moss; R A Lewis; W J Hall; J W MacCluer; P J Schwartz; E H Locati; D Tzivoni; G M Vincent; J L Robinson
Journal:  Am J Hum Genet       Date:  1994-12       Impact factor: 11.025

9.  High-risk long QT syndrome mutations in the Kv7.1 (KCNQ1) pore disrupt the molecular basis for rapid K(+) permeation.

Authors:  Don E Burgess; Daniel C Bartos; Allison R Reloj; Kenneth S Campbell; Jonathan N Johnson; David J Tester; Michael J Ackerman; Véronique Fressart; Isabelle Denjoy; Pascale Guicheney; Arthur J Moss; Seiko Ohno; Minoru Horie; Brian P Delisle
Journal:  Biochemistry       Date:  2012-11-02       Impact factor: 3.162

10.  Locus heterogeneity of autosomal dominant long QT syndrome.

Authors:  M Curran; D Atkinson; K Timothy; G M Vincent; A J Moss; M Leppert; M Keating
Journal:  J Clin Invest       Date:  1993-08       Impact factor: 14.808
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