Literature DB >> 16775115

Screening children with a family history of sudden cardiac death.

Christopher Wren1.   

Abstract

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Year:  2006        PMID: 16775115      PMCID: PMC1860723          DOI: 10.1136/hrt.2005.069757

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


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  20 in total

Review 1.  Long QT Syndrome.

Authors:  Arthur J Moss
Journal:  JAMA       Date:  2003 Apr 23-30       Impact factor: 56.272

2.  Value of electrocardiographic parameters and ajmaline test in the diagnosis of Brugada syndrome caused by SCN5A mutations.

Authors:  Kui Hong; Josep Brugada; Antonio Oliva; Antonio Berruezo-Sanchez; Domenico Potenza; Guido D Pollevick; Alejandra Guerchicoff; Kiyotaka Matsuo; Elena Burashnikov; Robert Dumaine; Jeffrey A Towbin; Vladislav Nesterenko; Pedro Brugada; Charles Antzelevitch; Ramon Brugada
Journal:  Circulation       Date:  2004-11-01       Impact factor: 29.690

Review 3.  Guidelines for the study of familial dilated cardiomyopathies. Collaborative Research Group of the European Human and Capital Mobility Project on Familial Dilated Cardiomyopathy.

Authors:  L Mestroni; B Maisch; W J McKenna; K Schwartz; P Charron; C Rocco; F Tesson; A Richter; A Wilke; M Komajda
Journal:  Eur Heart J       Date:  1999-01       Impact factor: 29.983

4.  Diagnostic value of electrocardiography and echocardiography for familial hypertrophic cardiomyopathy in genotyped children.

Authors:  P Charron; O Dubourg; M Desnos; J B Bouhour; R Isnard; A Hagege; L Carrier; G Bonne; F Tesson; P Richard; B Hainque; K Schwartz; M Komajda
Journal:  Eur Heart J       Date:  1998-09       Impact factor: 29.983

5.  Long-term outcome and prognostic determinants in children with hypertrophic cardiomyopathy.

Authors:  A T Yetman; R M Hamilton; L N Benson; B W McCrindle
Journal:  J Am Coll Cardiol       Date:  1998-12       Impact factor: 24.094

6.  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

Review 7.  Sudden death in patients without structural heart disease.

Authors:  Eric F D Wever; Etienne O Robles de Medina
Journal:  J Am Coll Cardiol       Date:  2004-04-07       Impact factor: 24.094

8.  Marfan syndrome in children and adolescents: predictive and prognostic value of aortic root growth for screening for aortic complications.

Authors:  M Groenink; L Rozendaal; M S Naeff; R C Hennekam; A A Hart; E E van der Wall; B J Mulder
Journal:  Heart       Date:  1998-08       Impact factor: 5.994

9.  Catecholaminergic polymorphic ventricular tachycardia in children. A 7-year follow-up of 21 patients.

Authors:  A Leenhardt; V Lucet; I Denjoy; F Grau; D D Ngoc; P Coumel
Journal:  Circulation       Date:  1995-03-01       Impact factor: 29.690

10.  Targeted mutational analysis of the RyR2-encoded cardiac ryanodine receptor in sudden unexplained death: a molecular autopsy of 49 medical examiner/coroner's cases.

Authors:  David J Tester; Daniel B Spoon; Hector H Valdivia; Jonathan C Makielski; Michael J Ackerman
Journal:  Mayo Clin Proc       Date:  2004-11       Impact factor: 7.616

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  5 in total

1.  Cardiogenetic counselling in a non-university hospital.

Authors:  J Kodde; N Hofman; C L A Reichert; I M van Langen; A A M Wilde
Journal:  Neth Heart J       Date:  2007-12       Impact factor: 2.380

2.  A review of sudden unexpected death in the young in British Columbia.

Authors:  Z Lim; K Gibbs; J Edward Potts; S Sanatani
Journal:  Can J Cardiol       Date:  2010-01       Impact factor: 5.223

3.  Genetic testing for long QT syndrome and the category of cardiac ion channelopathies.

Authors:  Stephen M Modell; David J Bradley; Michael H Lehmann
Journal:  PLoS Curr       Date:  2012-05-03

4.  Sudden cardiac death in young athletes; a literature review and special considerations in Asia.

Authors:  Farzin Halabchi; Tohid Seif-Barghi; Reza Mazaheri
Journal:  Asian J Sports Med       Date:  2011-03

5.  Novel Genetic Variants in BAG3 and TNNT2 in a Swedish Family with a History of Dilated Cardiomyopathy and Sudden Cardiac Death.

Authors:  Eva Fernlund; A Wålinder Österberg; E Kuchinskaya; M Gustafsson; K Jansson; C Gunnarsson
Journal:  Pediatr Cardiol       Date:  2017-07-01       Impact factor: 1.655

  5 in total

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