(Q38441528)

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Gene-specific modifying effects of pro-LVH polymorphisms involving the renin-angiotensin-aldosterone system among 389 unrelated patients with hypertrophic cardiomyopathy

scientific article published on 08 August 2005

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scholarly article

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Europe PubMed Central

PubMed publication ID

3 September 2017

Gene-specific modifying effects of pro-LVH polymorphisms involving the renin-angiotensin-aldosterone system among 389 unrelated patients with hypertrophic cardiomyopathy (English)

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Bernard J Gersh

5

object named as

Bernard J Gersh

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Michael J Ackerman

7

object named as

Michael J Ackerman

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

author name string

Meghan J Perkins

1

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Sara L Van Driest

2

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Erik G Ellsworth

3

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Melissa L Will

4

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Steve R Ommen

6

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

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publication date

8 August 2005

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Europe PubMed Central

PubMed publication ID

3 September 2017

European Heart Journal

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Europe PubMed Central

PubMed publication ID

3 September 2017

26

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Europe PubMed Central

PubMed publication ID

3 September 2017

22

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Europe PubMed Central

PubMed publication ID

3 September 2017

2457-2462

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

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

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHI438

21 January 2018

The management of hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHI438

21 January 2018

The Genetic Basis for Cardiomyopathy

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHI438

21 January 2018

Molecular genetic basis of hypertrophic cardiomyopathy: genetic markers for sudden cardiac death

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHI438

21 January 2018

New concepts in hypertrophic cardiomyopathies, part I.

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHI438

21 January 2018

Prognostic implications of novel beta cardiac myosin heavy chain gene mutations that cause familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHI438

21 January 2018

Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHI438

21 January 2018

A new missense mutation, Arg719Gln, in the beta-cardiac heavy chain myosin gene of patients with familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHI438

21 January 2018

Clinical Features of Hypertrophic Cardiomyopathy Caused by Mutation of a “Hot Spot” in the Alpha-Tropomyosin Gene

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHI438

21 January 2018

Homozygous mutation in cardiac troponin T: implications for hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHI438

21 January 2018

Sudden death due to troponin T mutations

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHI438

21 January 2018

Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHI438

21 January 2018

Genetic polymorphisms in the renin-angiotensin system: relevance for susceptibility to cardiovascular disease

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHI438

21 January 2018

Angiotensin-converting enzyme polymorphism in hypertrophic cardiomyopathy and sudden cardiac death

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHI438

21 January 2018

Angiotensin-Converting Enzyme and Heart Chymase gene Polymorphisms in Hypertrophic Cardiomyopathy**This study was supported by a grant-in-aid from the Bundesministerium für Bildung und Forschung and the European commission grant (ERBCHBGCT 940725

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHI438

21 January 2018

Angiotensinogen gene polymorphism in Japanese patients with hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHI438

21 January 2018

Associations between human aldosterone synthase (CYP11B2) gene polymorphisms and left ventricular size, mass, and function

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHI438

21 January 2018

Comprehensive analysis of the beta-myosin heavy chain gene in 389 unrelated patients with hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHI438

21 January 2018

Prevalence and spectrum of thin filament mutations in an outpatient referral population with hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHI438

21 January 2018

Prevalence and age-dependence of malignant mutations in the beta-myosin heavy chain and troponin T genes in hypertrophic cardiomyopathy: a comprehensive outpatient perspective

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHI438

21 January 2018

Prevalence and severity of "benign" mutations in the beta-myosin heavy chain, cardiac troponin T, and alpha-tropomyosin genes in hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHI438

21 January 2018

Identifiers

10.1093/EURHEARTJ/EHI438

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

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