Literature DB >> 18355655

The Brugada syndrome.

Peng-Sheng Chen, Silvia G Priori.   

Abstract

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Year:  2008        PMID： 18355655     DOI： 10.1016/j.jacc.2007.12.006

Source DB:  PubMed          Journal:  J Am Coll Cardiol        ISSN： 0735-1097            Impact factor:   24.094


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  11 in total

Review 1.  The molecular autopsy: should the evaluation continue after the funeral?

Authors:  David J Tester; Michael J Ackerman
Journal:  Pediatr Cardiol       Date:  2012-02-04       Impact factor: 1.655

Review 2.  Arrhythmia pharmacogenomics: methodological considerations.

Authors:  Dan M Roden; Prince J Kannankeri; Dawood Darbar
Journal:  Curr Pharm Des       Date:  2009       Impact factor: 3.116

Review 3.  Cardiac gene defects can cause sudden cardiac death in young people.

Authors:  Silke Kauferstein; Nadine Kiehne; Thomas Neumann; Heinz-Friedrich Pitschner; Hansjürgen Bratzke
Journal:  Dtsch Arztebl Int       Date:  2009-01-23       Impact factor: 5.594

4.  Transient outward current (I(to)) gain-of-function mutations in the KCND3-encoded Kv4.3 potassium channel and Brugada syndrome.

Authors:  John R Giudicessi; Dan Ye; David J Tester; Lia Crotti; Alessandra Mugione; Vladislav V Nesterenko; Richard M Albertson; Charles Antzelevitch; Peter J Schwartz; Michael J Ackerman
Journal:  Heart Rhythm       Date:  2011-02-22       Impact factor: 6.343

Review 5.  STRIPAK complexes: structure, biological function, and involvement in human diseases.

Authors:  Juyeon Hwang; David C Pallas
Journal:  Int J Biochem Cell Biol       Date:  2013-12-11       Impact factor: 5.085

Review 6.  Catecholaminergic polymorphic ventricular tachycardia.

Authors:  Kaisa Ylänen; Tuija Poutanen; Anita Hiippala; Heikki Swan; Matti Korppi
Journal:  Eur J Pediatr       Date:  2010-02-09       Impact factor: 3.183

Review 7.  Potassium-channel mutations and cardiac arrhythmias--diagnosis and therapy.

Authors:  John R Giudicessi; Michael J Ackerman
Journal:  Nat Rev Cardiol       Date:  2012-01-31       Impact factor: 32.419

Review 8.  Genetic testing for potentially lethal, highly treatable inherited cardiomyopathies/channelopathies in clinical practice.

Authors:  David J Tester; Michael J Ackerman
Journal:  Circulation       Date:  2011-03-08       Impact factor: 29.690

9.  An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing.

Authors:  Jamie D Kapplinger; David J Tester; Marielle Alders; Begoña Benito; Myriam Berthet; Josep Brugada; Pedro Brugada; Véronique Fressart; Alejandra Guerchicoff; Carole Harris-Kerr; Shiro Kamakura; Florence Kyndt; Tamara T Koopmann; Yoshihiro Miyamoto; Ryan Pfeiffer; Guido D Pollevick; Vincent Probst; Sven Zumhagen; Matteo Vatta; Jeffrey A Towbin; Wataru Shimizu; Eric Schulze-Bahr; Charles Antzelevitch; Benjamin A Salisbury; Pascale Guicheney; Arthur A M Wilde; Ramon Brugada; Jean-Jacques Schott; Michael J Ackerman
Journal:  Heart Rhythm       Date:  2009-10-08       Impact factor: 6.343

Review 10.  Genetic testing in heritable cardiac arrhythmia syndromes: differentiating pathogenic mutations from background genetic noise.

Authors:  John R Giudicessi; Michael J Ackerman
Journal:  Curr Opin Cardiol       Date:  2013-01       Impact factor: 2.161
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