(Q28239397)

2

0 references

Philippe Chevalier

3

0 references

Mohamed Chahine

4

0 references

Hai Huang

5

0 references

Daniel Malicier

6

0 references

Claire Rodriguez-Lafrasse

7

0 references

Robert Rousson

Long-QT syndrome-related sodium channel mutations probed by the dynamic action potential clamp technique.

8

0 references

language of work or name

English

0 references

publication date

May 2009

0 references

published in

Pediatric Cardiology

0 references

volume

30

0 references

issue

4

0 references

page(s)

502-9

0 references

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00246-009-9417-2

Artemis: guarding small children and, now, the genome

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00246-009-9417-2

Sudden cardiac death without structural heart disease: update on the long QT and Brugada syndromes

21 January 2018

1 reference

12 December 2020

Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing

1 reference

12 December 2020

Categories of preventable unexpected infant deaths

1 reference

12 December 2020

Spectrum and prevalence of cardiac sodium channel variants among black, white, Asian, and Hispanic individuals: implications for arrhythmogenic susceptibility and Brugada/long QT syndrome genetic testing

1 reference

12 December 2020

Functional characterization of the common amino acid 897 polymorphism of the cardiac potassium channel KCNH2 (HERG).

1 reference

12 December 2020

Cardiac sodium channel dysfunction in sudden infant death syndrome.

1 reference

12 December 2020

Sudden infant death syndrome: how significant are the cardiac channelopathies?

1 reference

12 December 2020

Postmortem molecular analysis of SCN5A defects in sudden infant death syndrome.

1 reference

12 December 2020

A founder mutation of the potassium channel KCNQ1 in long QT syndrome: implications for estimation of disease prevalence and molecular diagnostics

1 reference

12 December 2020

Prevalence of long-QT syndrome gene variants in sudden infant death syndrome

1 reference

12 December 2020

Possible association of the human KCNE1 (minK) gene and QT interval in healthy subjects: evidence from association and linkage analyses in Israeli families

1 reference

12 December 2020

Molecular and functional characterization of common polymorphisms in HERG (KCNH2) potassium channels

1 reference

12 December 2020

Novel mechanism for sudden infant death syndrome: persistent late sodium current secondary to mutations in caveolin-3

1 reference

12 December 2020

The use of genotype-phenotype correlations in mutation analysis for the long QT syndrome

1 reference

12 December 2020

Association of KCNQ1, KCNE1, KCNH2 and SCN5A polymorphisms with QTc interval length in a healthy population

1 reference

12 December 2020

Common Variants in Myocardial Ion Channel Genes Modify the QT Interval in the General Population

1 reference

12 December 2020

De novo mutation in the SCN5A gene associated with early onset of sudden infant death

1 reference

12 December 2020

A common polymorphism in KCNH2 (HERG) hastens cardiac repolarization

1 reference

12 December 2020

Cardiac sympathetic innervation and the sudden infant death syndrome. A possible pathogenetic link

1 reference

12 December 2020

Sudden infant death syndrome and long QT syndrome: an epidemiological and genetic study.

1 reference

12 December 2020

Prolongation of the QT interval and the sudden infant death syndrome.

1 reference

12 December 2020

A mechanism for sudden infant death syndrome (SIDS): stress-induced leak via ryanodine receptors

1 reference

12 December 2020

Survey of the coding region of the HERG gene in long QT syndrome reveals six novel mutations and an amino acid polymorphism with possible phenotypic effects

1 reference

12 December 2020

Molecular diagnosis in a child with sudden infant death syndrome

1 reference

12 December 2020

Sudden Infant Death Syndrome: review of implicated genetic factors

1 reference

12 December 2020

Common human SCN5A polymorphisms have altered electrophysiology when expressed in Q1077 splice variants

1 reference

12 December 2020

A common cardiac sodium channel variant associated with sudden infant death in African Americans, SCN5A S1103Y

1 reference

12 December 2020

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

1 reference

12 December 2020

Spectrum of pathogenic mutations and associated polymorphisms in a cohort of 44 unrelated patients with long QT syndrome

1 reference

12 December 2020

Long QT syndrome in neonates: conduction disorders associated with HERG mutations and sinus bradycardia with KCNQ1 mutations

1 reference

12 December 2020

Molecular and functional characterization of novel glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) mutations in sudden infant death syndrome

1 reference

12 December 2020

A common SCN5A polymorphism modulates the biophysical effects of an SCN5A mutation

1 reference

12 December 2020

Potential role of QT interval prolongation in sudden infant death syndrome

1 reference

12 December 2020

KCNH2-K897T is a genetic modifier of latent congenital long-QT syndrome

1 reference

12 December 2020

Mutations in the HERG K+-ion channel: A novel link between long QT syndrome and sudden infant death syndrome

1 reference

12 December 2020