(Q36593290)

15 August 2017

Torsades de pointes following acute myocardial infarction: evidence for a deadly link with a common genetic variant (English)

1 reference

acute myocardial infarction

15 August 2017

1 reference

1 reference

Federica Dagradi

8

0 references

Antonio Oliva

Antonio Oliva

5

0 references

Lia Crotti

Lia Crotti

1

0 references

Peter J. Schwartz

Peter J Schwartz

11

0 references

Charles Antzelevitch

13

14

Charles Antzelevitch

1 reference

15 August 2017

Dan Hu

2

1 reference

15 August 2017

Hector Barajas-Martinez

3

1 reference

15 August 2017

Gaetano M De Ferrari

4

1 reference

15 August 2017

Roberto Insolia

6

1 reference

15 August 2017

Guido D Pollevick

7

1 reference

15 August 2017

Alejandra Guerchicoff

9

1 reference

15 August 2017

Federica Greco

10

1 reference

15 August 2017

Sami Viskin

12

1 reference

15 August 2017

13 February 2012

1 reference

15 August 2017

1 reference

15 August 2017

9

1 reference

15 August 2017

7

1 reference

15 August 2017

1104-1112

1 reference

Long-QT syndrome: from genetics to management

15 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3566559

A large candidate gene survey identifies the KCNE1 D85N polymorphism as a possible modulator of drug-induced torsades de pointes

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3566559

Genome-wide association study identifies a susceptibility locus at 21q21 for ventricular fibrillation in acute myocardial infarction

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3566559

Active cascade screening in primary inherited arrhythmia syndromes: does it lead to prophylactic treatment?

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3566559

A common single nucleotide polymorphism can exacerbate long-QT type 2 syndrome leading to sudden infant death.

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3566559

The response of the QT interval to the brief tachycardia provoked by standing: a bedside test for diagnosing long QT syndrome

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3566559

Prevalence of the congenital long-QT syndrome.

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3566559

NOS1AP is a genetic modifier of the long-QT syndrome

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3566559

Common variants at ten loci influence QT interval duration in the QTGEN Study

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3566559

Genetic variations in nitric oxide synthase 1 adaptor protein are associated with sudden cardiac death in US white community-based populations

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3566559

Determinants of prolonged QT interval and their contribution to sudden death risk in coronary artery disease: the Oregon Sudden Unexpected Death Study

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3566559

The human ERG1 channel polymorphism, K897T, creates a phosphorylation site that inhibits channel activity

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3566559

Novel mutation in the SCN5A gene associated with arrhythmic storm development during acute myocardial infarction

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3566559

A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3566559

Rac GTPase signaling through the PP5 protein phosphatase

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3566559

Rapid signaling at the plasma membrane by a nuclear receptor for thyroid hormone

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3566559

Increased risk of arrhythmic events in long-QT syndrome with mutations in the pore region of the human ether-a-go-go-related gene potassium channel

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3566559

Linkage and mutation analysis in two Taiwanese families with long QT syndrome.

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3566559

Sudden death due to cardiac arrhythmias

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3566559

Family history as a risk factor for primary cardiac arrest

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3566559

Hardy-Weinberg equilibrium testing of biological ascertainment for Mendelian randomization studies

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3566559

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

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3566559

Polymorphisms in the NOS1AP gene modulate QT interval duration and risk of arrhythmias in the long QT syndrome.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3566559

Cascades or waterfalls, the cataracts of genetic screening are being opened on clinical cardiology.

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3566559

Familial sudden death is an important risk factor for primary ventricular fibrillation: a case-control study in acute myocardial infarction patients

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3566559

Cellular basis for complex T waves and arrhythmic activity following combined I(Kr) and I(Ks) block

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3566559

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

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3566559

Family history and the risk of sudden cardiac death as a manifestation of an acute coronary event

4 December 2018

1 reference

12 December 2020

Acquired long QT syndrome from stress cardiomyopathy is associated with ventricular arrhythmias and torsades de pointes

1 reference

12 December 2020

Pause-dependent torsade de pointes following acute myocardial infarction: a variant of the acquired long QT syndrome

1 reference

12 December 2020

A common polymorphism in KCNH2 (HERG) hastens cardiac repolarization

1 reference

12 December 2020

QT interval prolongation as predictor of sudden death in patients with myocardial infarction

1 reference

12 December 2020

Predicting sudden death in the population: the Paris Prospective Study I

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

10.1016/J.HRTHM.2012.02.014

Identifiers

DOI

1 reference

15 August 2017

1 reference

15 August 2017

PubMed publication ID

22338672

1 reference