(Q44019185)

29 November 2017

Novel mutations in domain I of SCN5A cause Brugada syndrome (English)

1 reference

29 November 2017

3

1 reference

29 November 2017

4

1 reference

29 November 2017

Josep Brugada

9

1 reference

ORCID Public Data File 2021

Jeffrey A Towbin

series ordinal

11

object named as

Jeffrey A Towbin

1 reference

29 November 2017

10

Pedro Brugada

1 reference

29 November 2017

5

Ramon Brugada

1 reference

29 November 2017

2

Robert Dumaine

1 reference

29 November 2017

8

Koonlawee Nademanee

1 reference

29 November 2017

1

Matteo Vatta

1 reference

29 November 2017

7

Neil E Bowles

1 reference

29 November 2017

Hua Li

6

1 reference

29 November 2017

1 April 2002

1 reference

Molecular Genetics and Metabolism

29 November 2017

1 reference

29 November 2017

75

1 reference

29 November 2017

317-324

1 reference

29 November 2017

4

1 reference

Right bundle branch block, persistent ST segment elevation and sudden cardiac death: A distinct clinical and electrocardiographic syndrome

29 November 2017

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900006-9

7 January 2021

Further characterization of the syndrome of right bundle branch block, ST segment elevation, and sudden cardiac death

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900006-9

7 January 2021

The Brugada syndrome: clinical, electrophysiologic and genetic aspects.

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900006-9

7 January 2021

Ion channels and ventricular arrhythmias: cellular and ionic mechanisms underlying the Brugada syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900006-9

7 January 2021

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900006-9

7 January 2021

Arrhythmogenic marker for the sudden unexplained death syndrome in Thai men.

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900006-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900006-9

7 January 2021

Multiple mechanisms of Na+ channel--linked long-QT syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900006-9

7 January 2021

Molecular mechanism for an inherited cardiac arrhythmia

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900006-9

7 January 2021

Cardiac conduction defects associate with mutations in SCN5A

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900006-9

7 January 2021

A sodium-channel mutation causes isolated cardiac conduction disease

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900006-9

7 January 2021

A molecular link between the sudden infant death syndrome and the long-QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900006-9

7 January 2021

Ionic mechanisms responsible for the electrocardiographic phenotype of the Brugada syndrome are temperature dependent

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900006-9

7 January 2021

Human SCN5A gene mutations alter cardiac sodium channel kinetics and are associated with the Brugada syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900006-9

7 January 2021

A single Na(+) channel mutation causing both long-QT and Brugada syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900006-9

7 January 2021

Electrophysiological characterization of SCN5A mutations causing long QT (E1784K) and Brugada (R1512W and R1432G) syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900006-9

7 January 2021

Enhanced Na(+) channel intermediate inactivation in Brugada syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900006-9

7 January 2021

"Brugada" syndrome: clinical data and suggested pathophysiological mechanism

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900006-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900006-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900006-9

7 January 2021

A routine method for the establishment of permanent growing lymphoblastoid cell lines

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900006-9

7 January 2021

Genomic structure of three long QT syndrome genes: KVLQT1, HERG, and KCNE1.

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900006-9

7 January 2021

Detection of numerous Y chromosome biallelic polymorphisms by denaturing high-performance liquid chromatography

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900006-9

7 January 2021

Effects of III-IV linker mutations on human heart Na+ channel inactivation gating

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900006-9

7 January 2021

Structure and function of voltage-gated sodium channels

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900006-9

7 January 2021

Brugada syndrome and sudden cardiac death in children

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900006-9

7 January 2021

Molecular biology of arrhythmic syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900006-9

7 January 2021

Cardiac arrhythmias: the genetic connection

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900006-9

7 January 2021

10.1016/S1096-7192(02)00006-9

Identifiers

DOI

1 reference

29 November 2017

1 reference

PubMed ID

12051963