(Q33165997)

23 July 2017

Rare genetic variants previously associated with congenital forms of long QT syndrome have little or no effect on the QT interval (English)

1 reference

23 July 2017

0 references

1 reference

10

1 reference

23 July 2017

8

Tea Skaaby

0 references

Jesper Hastrup Svendsen

14

Jesper Hastrup Svendsen

0 references

Stig Haunsø

13

Stig Haunsø

1 reference

23 July 2017

Gustav Ahlberg

5

0 references

Christian T Have

Christian Theil Have

2

0 references

Morten Salling Olesen

Morten Salling Olesen

17

0 references

Søren-Peter Olesen

Søren-Peter Olesen

9

0 references

Torben Hansen

Torben Hansen

15

0 references

Allan Linneberg

Allan Linneberg

11

0 references

Oluf Borbye Pedersen

Oluf Pedersen

12

0 references

Peter E Weeke

3

Peter Weeke

1 reference

23 July 2017

4

Jonas Bille Nielsen

1 reference

23 July 2017

6

Marie Balslev-Harder

1 reference

23 July 2017

1

Jonas Ghouse

1 reference

23 July 2017

7

Emil Vincent Appel

1 reference

23 July 2017

Jørgen Kim Kanters

16

1 reference

23 July 2017

9 July 2015

1 reference

23 July 2017

European Heart Journal

1 reference

23 July 2017

36

1 reference

23 July 2017

37

1 reference

23 July 2017

2523-2529

1 reference

HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes: document endorsed by HRS, EHRA, and APHRS in May 2013 and by ACCF, AHA, PACES, and AEPC in June 2013.

23 July 2017

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHV297

The current role of next-generation DNA sequencing in routine care of patients with hereditary cardiovascular conditions: a viewpoint paper of the European Society of Cardiology working group on myocardial and pericardial diseases and members of the

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHV297

New population-based exome data are questioning the pathogenicity of previously cardiomyopathy-associated genetic variants

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHV297

High prevalence of genetic variants previously associated with LQT syndrome in new exome data

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHV297

Prevalences of diabetes and impaired glucose regulation in a Danish population: the Inter99 study

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHV297

A randomized non-pharmacological intervention study for prevention of ischaemic heart disease: baseline results Inter99.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHV297

Whole-exome sequencing of 2,000 Danish individuals and the role of rare coding variants in type 2 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHV297

Diagnostic criteria for the long QT syndrome. An update

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHV297

Prevention of torsade de pointes in hospital settings: a scientific statement from the American Heart Association and the American College of Cardiology Foundation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHV297

Accuracy of the ICD-10 discharge diagnosis for syncope

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHV297

PLINK: a tool set for whole-genome association and population-based linkage analyses

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHV297

Prevalence of the congenital long-QT syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHV297

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHV297

Long-QT syndrome after age 40.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHV297

Mutant caveolin-3 induces persistent late sodium current and is associated with long-QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHV297

The role of CAV3 in long-QT syndrome: clinical and functional assessment of a caveolin-3/Kv11.1 double heterozygote versus caveolin-3 single heterozygote

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHV297

Diagnostic miscues in congenital long-QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHV297

21 January 2018

Identifiers

DOI

10.1093/EURHEARTJ/EHV297

1 reference

23 July 2017

1 reference

PubMed ID

26159999