Literature DB >> 9038683

Is long QT syndrome entering the era of molecular diagnosis?

S G Priori.   

Abstract

Entities:  

Mesh：

Year:  1997        PMID： 9038683      PMCID： PMC484623          DOI： 10.1136/hrt.77.1.5

Source DB:  PubMed          Journal:  Heart        ISSN： 1355-6037            Impact factor:   5.994


× No keyword cloud information.
  16 in total

1.  Idiopathic long QT syndrome: progress and questions.

Authors:  P J Schwartz
Journal:  Am Heart J       Date:  1985-02       Impact factor: 4.749

2.  Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy.

Authors:  H Watkins; A Rosenzweig; D S Hwang; T Levi; W McKenna; C E Seidman; J G Seidman
Journal:  N Engl J Med       Date:  1992-04-23       Impact factor: 91.245

3.  Spectrum of HERG K+-channel dysfunction in an inherited cardiac arrhythmia.

Authors:  M C Sanguinetti; M E Curran; P S Spector; M T Keating
Journal:  Proc Natl Acad Sci U S A       Date:  1996-03-05       Impact factor: 11.205

4.  Evidence of genetic heterogeneity in Romano-Ward long QT syndrome. Analysis of 23 families.

Authors:  J A Towbin; H Li; R T Taggart; M H Lehmann; P J Schwartz; C A Satler; R Ayyagari; J L Robinson; A Moss; J F Hejtmancik
Journal:  Circulation       Date:  1994-12       Impact factor: 29.690

5.  Cardiac sodium channel mutations in patients with long QT syndrome, an inherited cardiac arrhythmia.

Authors:  Q Wang; J Shen; Z Li; K Timothy; G M Vincent; S G Priori; P J Schwartz; M T Keating
Journal:  Hum Mol Genet       Date:  1995-09       Impact factor: 6.150

6.  Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneity.

Authors:  C Jiang; D Atkinson; J A Towbin; I Splawski; M H Lehmann; H Li; K Timothy; R T Taggart; P J Schwartz; G M Vincent
Journal:  Nat Genet       Date:  1994-10       Impact factor: 38.330

7.  Molecular mechanism for an inherited cardiac arrhythmia.

Authors:  P B Bennett; K Yazawa; N Makita; A L George
Journal:  Nature       Date:  1995-08-24       Impact factor: 49.962

8.  SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome.

Authors:  Q Wang; J Shen; I Splawski; D Atkinson; Z Li; J L Robinson; A J Moss; J A Towbin; M T Keating
Journal:  Cell       Date:  1995-03-10       Impact factor: 41.582

9.  A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome.

Authors:  M E Curran; I Splawski; K W Timothy; G M Vincent; E D Green; M T Keating
Journal:  Cell       Date:  1995-03-10       Impact factor: 41.582

10.  Mapping of a gene for long QT syndrome to chromosome 4q25-27.

Authors:  J J Schott; F Charpentier; S Peltier; P Foley; E Drouin; J B Bouhour; P Donnelly; G Vergnaud; L Bachner; J P Moisan
Journal:  Am J Hum Genet       Date:  1995-11       Impact factor: 11.025
View more
  1 in total

Review 1.  The risk of cardiac events and genotype-based management of LQTS patients.

Authors:  Grazyna Markiewicz-Łoskot; Ewa Moric-Janiszewska; Urszula Mazurek
Journal:  Ann Noninvasive Electrocardiol       Date:  2009-01       Impact factor: 1.468
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.