Literature DB >> 17556198

Genetic basis of Brugada syndrome.

Charles Antzelevitch.   

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Year:  2007        PMID: 17556198      PMCID: PMC1989771          DOI: 10.1016/j.hrthm.2007.03.015

Source DB:  PubMed          Journal:  Heart Rhythm        ISSN: 1547-5271            Impact factor:   6.343


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  17 in total

1.  Exclusion of multiple candidate genes and large genomic rearrangements in SCN5A in a Dutch Brugada syndrome cohort.

Authors:  Tamara T Koopmann; Leander Beekman; Marielle Alders; Paola G Meregalli; Marcel M A M Mannens; Antoon F M Moorman; Arthur A M Wilde; Connie R Bezzina
Journal:  Heart Rhythm       Date:  2007-03-02       Impact factor: 6.343

2.  Effect of sodium channel blockers on ST segment, QRS duration, and corrected QT interval in patients with Brugada syndrome.

Authors:  W Shimizu; C Antzelevitch; K Suyama; T Kurita; A Taguchi; N Aihara; H Takaki; K Sunagawa; S Kamakura
Journal:  J Cardiovasc Electrophysiol       Date:  2000-12

3.  Sodium channel blockers identify risk for sudden death in patients with ST-segment elevation and right bundle branch block but structurally normal hearts.

Authors:  R Brugada; J Brugada; C Antzelevitch; G E Kirsch; D Potenza; J A Towbin; P Brugada
Journal:  Circulation       Date:  2000-02-08       Impact factor: 29.690

4.  Patterning the embryonic heart: identification of five mouse Iroquois homeobox genes in the developing heart.

Authors:  V M Christoffels; A G Keijser; A C Houweling; D E Clout; A F Moorman
Journal:  Dev Biol       Date:  2000-08-15       Impact factor: 3.582

5.  Bop encodes a muscle-restricted protein containing MYND and SET domains and is essential for cardiac differentiation and morphogenesis.

Authors:  Paul D Gottlieb; Stephanie A Pierce; Robert J Sims; Hiroyuki Yamagishi; Elizabeth K Weihe; June V Harriss; Shanna D Maika; William A Kuziel; Heather L King; Eric N Olson; Osamu Nakagawa; Deepak Srivastava
Journal:  Nat Genet       Date:  2002-04-01       Impact factor: 38.330

6.  Clinical and genetic heterogeneity of right bundle branch block and ST-segment elevation syndrome: A prospective evaluation of 52 families.

Authors:  S G Priori; C Napolitano; M Gasparini; C Pappone; P Della Bella; M Brignole; U Giordano; T Giovannini; C Menozzi; R Bloise; L Crotti; L Terreni; P J Schwartz
Journal:  Circulation       Date:  2000-11-14       Impact factor: 29.690

7.  Clinical and molecular heterogeneity in the Brugada syndrome: a novel gene locus on chromosome 3.

Authors:  Raul Weiss; M Michael Barmada; Tuduy Nguyen; Jolene S Seibel; Doris Cavlovich; Cari A Kornblit; Adam Angelilli; Flordeliza Villanueva; Dennis M McNamara; Barry London
Journal:  Circulation       Date:  2002-02-12       Impact factor: 29.690

8.  Genetic basis and molecular mechanism for idiopathic ventricular fibrillation.

Authors:  Q Chen; G E Kirsch; D Zhang; R Brugada; J Brugada; P Brugada; D Potenza; A Moya; M Borggrefe; G Breithardt; R Ortiz-Lopez; Z Wang; C Antzelevitch; R E O'Brien; E Schulze-Bahr; M T Keating; J A Towbin; Q Wang
Journal:  Nature       Date:  1998-03-19       Impact factor: 49.962

9.  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

10.  Sodium channel gene (SCN5A) mutations in 44 index patients with Brugada syndrome: different incidences in familial and sporadic disease.

Authors:  Eric Schulze-Bahr; Lars Eckardt; Günter Breithardt; Karlheinz Seidl; Thomas Wichter; Christian Wolpert; Martin Borggrefe; Wilhelm Haverkamp
Journal:  Hum Mutat       Date:  2003-06       Impact factor: 4.878

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  6 in total

1.  An atypical case of Brugada syndrome.

Authors:  Almpanis Georgios; Servos Georgios; Tragotsalou Nikolitsa; Koutsogiannou Persefoni; Mazarakis Andreas
Journal:  Ann Noninvasive Electrocardiol       Date:  2011-10       Impact factor: 1.468

2.  Gain-of-function mutation S422L in the KCNJ8-encoded cardiac K(ATP) channel Kir6.1 as a pathogenic substrate for J-wave syndromes.

Authors:  Argelia Medeiros-Domingo; Bi-Hua Tan; Lia Crotti; David J Tester; Lee Eckhardt; Alessandra Cuoretti; Stacie L Kroboth; Chunhua Song; Qing Zhou; Doug Kopp; Peter J Schwartz; Jonathan C Makielski; Michael J Ackerman
Journal:  Heart Rhythm       Date:  2010-06-15       Impact factor: 6.343

3.  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

4.  Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test.

Authors:  Jamie D Kapplinger; David J Tester; Benjamin A Salisbury; Janet L Carr; Carole Harris-Kerr; Guido D Pollevick; Arthur A M Wilde; Michael J Ackerman
Journal:  Heart Rhythm       Date:  2009-06-23       Impact factor: 6.343

5.  Study of the extent of the information of cardiologists from São Paulo city, Brazil, regarding a low-prevalence entity: Brugada syndrome.

Authors:  Andrés Ricardo Pérez Riera; Celso F Filho; Augusto H Uchida; Li Zhang; Charles Antzelevitch; Edgardo Schapachnik; Sergio Dubner; Celso Ferreira
Journal:  Ann Noninvasive Electrocardiol       Date:  2008-10       Impact factor: 1.468

6.  Inherited arrhythmias in children.

Authors:  Seshadri Balaji
Journal:  Indian Pacing Electrophysiol J       Date:  2008-05-01
  6 in total

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