Literature DB >> 12750212

Variable presentation of Brugada syndrome: lessons from three generations with syncope.

Adrian Plunkett1, J A Hulse, B Mishra, J Gill.   

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Year:  2003        PMID: 12750212      PMCID: PMC1125991          DOI: 10.1136/bmj.326.7398.1078

Source DB:  PubMed          Journal:  BMJ        ISSN: 0959-8138


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  8 in total

Review 1.  Cardiac arrhythmias: the genetic connection.

Authors:  J A Towbin
Journal:  J Cardiovasc Electrophysiol       Date:  2000-05

2.  Right ventricular cardiomyopathy showing right bundle branch block and right precordial ST segment elevation.

Authors:  T Izumi; K Ajiki; A Nozaki; S Takahashi; F Tabei; H Hayakawa; T Sugimoto
Journal:  Intern Med       Date:  2000-01       Impact factor: 1.271

Review 3.  The Brugada syndrome: clinical, genetic, cellular, and molecular abnormalities.

Authors:  G V Naccarelli; C Antzelevitch
Journal:  Am J Med       Date:  2001-05       Impact factor: 4.965

Review 4.  What is the Brugada syndrome?

Authors:  D Corrado; G Buja; C Basso; A Nava; G Thiene
Journal:  Cardiol Rev       Date:  1999 Jul-Aug       Impact factor: 2.644

5.  Right bundle-branch block and ST-segment elevation in leads V1 through V3: a marker for sudden death in patients without demonstrable structural heart disease.

Authors:  J Brugada; R Brugada; P Brugada
Journal:  Circulation       Date:  1998-02-10       Impact factor: 29.690

Review 6.  The Brugada syndrome.

Authors:  P Brugada; R Brugada; J Brugada
Journal:  Curr Cardiol Rep       Date:  2000-11       Impact factor: 2.931

7.  Right bundle branch block, persistent ST segment elevation and sudden cardiac death: a distinct clinical and electrocardiographic syndrome. A multicenter report.

Authors:  P Brugada; J Brugada
Journal:  J Am Coll Cardiol       Date:  1992-11-15       Impact factor: 24.094

8.  Epidemiology of idiopathic dilated and hypertrophic cardiomyopathy. A population-based study in Olmsted County, Minnesota, 1975-1984.

Authors:  M B Codd; D D Sugrue; B J Gersh; L J Melton
Journal:  Circulation       Date:  1989-09       Impact factor: 29.690

  8 in total
  3 in total

1.  A common SCN5A polymorphism attenuates a severe cardiac phenotype caused by a nonsense SCN5A mutation in a Chinese family with an inherited cardiac conduction defect.

Authors:  Dau-Ming Niu; Betau Hwang; Han-Wei Hwang; Nana H Wang; Jer-Yuarn Wu; Pi-Chang Lee; Jen-Chung Chien; Ru-Chi Shieh; Yuan-Tsong Chen
Journal:  J Med Genet       Date:  2006-05-17       Impact factor: 6.318

2.  Brugada-like syndrome in infancy presenting with rapid ventricular tachycardia and intraventricular conduction delay.

Authors:  Ronald J Kanter; Ryan Pfeiffer; Dan Hu; Héctor Barajas-Martinez; Michael P Carboni; Charles Antzelevitch
Journal:  Circulation       Date:  2011-11-16       Impact factor: 29.690

Review 3.  Electrical heart disease: Genetic and molecular basis of cardiac arrhythmias in normal structural hearts.

Authors:  David Farwell; Michael H Gollob
Journal:  Can J Cardiol       Date:  2007-08       Impact factor: 5.223

  3 in total

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