(Q33153638)

22 July 2017

1 reference

title

The long QT syndrome family of cardiac ion channelopathies: a HuGE review (English)

1 reference

22 July 2017

1 reference

Stephen M Modell

1

1 reference

22 July 2017

Michael H Lehmann

series ordinal

2

1 reference

22 July 2017

language of work or name

English

0 references

publication date

1 March 2006

1 reference

22 July 2017

1 reference

22 July 2017

8

1 reference

22 July 2017

3

1 reference

22 July 2017

143-155

1 reference

https://scigraph.springernature.com/pub.10.1097/01.gim.0000204468.85308.86

22 July 2017

0 references

cites work

The long QT syndromes: genetic basis and clinical implications

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000204468.85308.86

Inherited long QT syndromes: a paradigm for understanding arrhythmogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000204468.85308.86

Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmias.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000204468.85308.86

Mutation site-specific differences in arrhythmic risk and sensitivity to sympathetic stimulation in the LQT1 form of congenital long QT syndrome: multicenter study in Japan

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000204468.85308.86

Four potassium channel mutations account for 73% of the genetic spectrum underlying long-QT syndrome (LQTS) and provide evidence for a strong founder effect in Finland

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000204468.85308.86

Bradycardia-induced long QT syndrome caused by a de novo missense mutation in the S2-S3 inner loop of HERG.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000204468.85308.86

A novel long-QT 5 gene mutation in the C-terminus (V109I) is associated with a mild phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000204468.85308.86

Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000204468.85308.86

Risk stratification in the long-QT syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000204468.85308.86

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000204468.85308.86

Evidence for a single nucleotide polymorphism in the KCNQ1 potassium channel that underlies susceptibility to life-threatening arrhythmias

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000204468.85308.86

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000204468.85308.86

Allelic variants in long-QT disease genes in patients with drug-associated torsades de pointes

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000204468.85308.86

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000204468.85308.86

Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000204468.85308.86

Modulating effects of age and gender on the clinical course of long QT syndrome by genotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000204468.85308.86

Mutational spectrum in the cardioauditory syndrome of Jervell and Lange-Nielsen.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000204468.85308.86

Mutation analysis in congenital Long QT Syndrome--a case with missense mutations in KCNQ1 and SCN5A.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000204468.85308.86

The implications of genetic mutations in the sodium channel gene (SCN5A).

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000204468.85308.86

Natural history of Brugada syndrome: insights for risk stratification and management

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000204468.85308.86

In vivo human demonstration of phase 2 reentry

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000204468.85308.86

Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A)

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000204468.85308.86

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000204468.85308.86

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000204468.85308.86

Measures of cardiac repolarization and body position in infants.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000204468.85308.86

Identification of a genetic locus for familial atrial fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000204468.85308.86

KCNQ1 gain-of-function mutation in familial atrial fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000204468.85308.86

Short QT Syndrome: a familial cause of sudden death

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000204468.85308.86

Asthma and the risk of cardiac events in the Long QT syndrome. Long QT Syndrome Investigative Group

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000204468.85308.86

A common human SCN5A polymorphism modifies expression of an arrhythmia causing mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000204468.85308.86

Female gender as a risk factor for torsades de pointes associated with cardiovascular drugs

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000204468.85308.86

Diagnostic criteria for the long QT syndrome. An update

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000204468.85308.86

QT dispersion: time for an obituary?

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000204468.85308.86

Sinus node function and ventricular repolarization during exercise stress test in long QT syndrome patients with KvLQT1 and HERG potassium channel defects.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000204468.85308.86

Epinephrine unmasks latent mutation carriers with LQT1 form of congenital long-QT syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000204468.85308.86

Long QT syndrome in children: the value of the rate corrected QT interval in children who present with fainting

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000204468.85308.86

Family and population strategies for screening and counselling of inherited cardiac arrhythmias

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000204468.85308.86

Task Force on Sudden Cardiac Death of the European Society of Cardiology.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000204468.85308.86

Recommendations for physical activity and recreational sports participation for young patients with genetic cardiovascular diseases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000204468.85308.86

Twenty single nucleotide polymorphisms (SNPs) and their allelic frequencies in four genes that are responsible for familial long QT syndrome in the Japanese population

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000204468.85308.86

Sex differences in phenotypic manifestation and gene transmission in the Romano-Ward syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000204468.85308.86

Electrocardiographic Prediction of Abnormal Genotype in Congenital Long QT Syndrome: Experience in 101 Related Family Members

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000204468.85308.86

Guidelines for the interpretation of the neonatal electrocardiogram

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000204468.85308.86

10.1097/01.GIM.0000204468.85308.86

21 January 2018

Identifiers

DOI

1 reference

Dimensions Publication ID

22 July 2017

0 references

1 reference