(Q37078819)

18 August 2017

1 reference

title

Family history: an essential tool for cardiovascular genetic medicine (English)

1 reference

18 August 2017

1 reference

Ana Morales

1

1 reference

18 August 2017

Jason Cowan

series ordinal

2

1 reference

18 August 2017

Jimena Dagua

series ordinal

3

1 reference

18 August 2017

Ray E Hershberger

series ordinal

4

1 reference

18 August 2017

publication date

1 January 2008

1 reference

18 August 2017

published in

Congestive Heart Failure

1 reference

18 August 2017

volume

14

1 reference

18 August 2017

issue

1

1 reference

18 August 2017

page(s)

37-45

1 reference

American College of Cardiology/European Society of Cardiology clinical expert consensus document on hypertrophic cardiomyopathy. A report of the American College of Cardiology Foundation Task Force on Clinical Expert Consensus Documents and the Euro

18 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08201.X

A contemporary approach to hypertrophic cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08201.X

Report of the WHO/ISFC task force on the definition and classification of cardiomyopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08201.X

Clinical and genetic issues in familial dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08201.X

The genetic family history assessment in gastroenterology nursing practice

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08201.X

Sudden death in young athletes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08201.X

The inheritance of hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08201.X

Prevalence of hypertrophic cardiomyopathy in a general population of young adults. Echocardiographic analysis of 4111 subjects in the CARDIA Study. Coronary Artery Risk Development in (Young) Adults

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08201.X

Prevalence of Anderson-Fabry disease in male patients with late onset hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08201.X

Genetic aspects of arrhythmias

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08201.X

Role of genetic analysis in the management of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08201.X

The long QT syndrome and seizures in childhood.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08201.X

The spectrum of symptoms and QT intervals in carriers of the gene for the long-QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08201.X

The long QT syndrome: a prospective international study

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08201.X

Short QT syndrome. Genotype-phenotype correlations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08201.X

Sudden death associated with short-QT syndrome linked to mutations in HERG.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08201.X

Catecholaminergic polymorphic ventricular tachycardia in children. A 7-year follow-up of 21 patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08201.X

Clinical and molecular characterization of patients with catecholaminergic polymorphic ventricular tachycardia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08201.X

The role of molecular autopsy in unexplained sudden cardiac death

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08201.X

Clinical genetics in cardiology

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08201.X

Genetic testing in cardiovascular disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08201.X

Genetics of dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08201.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08201.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08201.X

Screening children with a family history of sudden cardiac death

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08201.X

Spectrum and frequency of cardiac channel defects in swimming-triggered arrhythmia syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08201.X

Advances in the diagnostic management of arrhythmogenic right ventricular dysplasia-cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08201.X

How Really Rare Are Rare Diseases?:

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1751-7133.2008.08201.X

10.1111/J.1751-7133.2008.08201.X

21 January 2018

Identifiers

DOI

1 reference

18 August 2017

1 reference