(Q47886356)

English

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

scientific article published in June 2002

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scholarly article

1 reference

Europe PubMed Central

6 February 2018

http://europepmc.org/abstract/MED/12084606

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

1 reference

Europe PubMed Central

6 February 2018

http://europepmc.org/abstract/MED/12084606

hypertrophic cardiomyopathy

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Bernard J Gersh

7

object named as

Bernard J Gersh

1 reference

Europe PubMed Central

6 February 2018

http://europepmc.org/abstract/MED/12084606

Michael J Ackerman

1

object named as

Michael J Ackerman

1 reference

Europe PubMed Central

6 February 2018

http://europepmc.org/abstract/MED/12084606

author name string

Sara L VanDriest

2

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Europe PubMed Central

6 February 2018

http://europepmc.org/abstract/MED/12084606

Steve R Ommen

3

1 reference

Europe PubMed Central

6 February 2018

http://europepmc.org/abstract/MED/12084606

Melissa L Will

4

1 reference

Europe PubMed Central

6 February 2018

http://europepmc.org/abstract/MED/12084606

Rick A Nishimura

5

1 reference

Europe PubMed Central

6 February 2018

http://europepmc.org/abstract/MED/12084606

A Jamil Tajik

6

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Europe PubMed Central

6 February 2018

http://europepmc.org/abstract/MED/12084606

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publication date

1 June 2002

1 reference

Europe PubMed Central

6 February 2018

http://europepmc.org/abstract/MED/12084606

Journal of the American College of Cardiology

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Europe PubMed Central

6 February 2018

http://europepmc.org/abstract/MED/12084606

39

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Europe PubMed Central

6 February 2018

http://europepmc.org/abstract/MED/12084606

2042-2048

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Europe PubMed Central

6 February 2018

http://europepmc.org/abstract/MED/12084606

12

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Europe PubMed Central

6 February 2018

http://europepmc.org/abstract/MED/12084606

Hypertrophie cardiomyopathy: A discussion of nomenclature

1 reference

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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

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Hypertrophic cardiomyopathy. Interrelations of clinical manifestations, pathophysiology, and therapy (1).

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Efficacy of Implantable Cardioverter–Defibrillators for the Prevention of Sudden Death in Patients with Hypertrophic Cardiomyopathy

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

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A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation

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Structural interpretation of the mutations in the beta-cardiac myosin that have been implicated in familial hypertrophic cardiomyopathy

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Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere

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Sudden death due to troponin T mutations

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The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigms

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Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy

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Inherited and de novo mutations in the cardiac actin gene cause hypertrophic cardiomyopathy

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Alpha-cardiac actin is a novel disease gene in familial hypertrophic cardiomyopathy

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Structural analysis of the titin gene in hypertrophic cardiomyopathy: identification of a novel disease gene

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

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Molecular genetics of familial hypertrophic cardiomyopathy

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

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Differences in clinical expression of hypertrophic cardiomyopathy associated with two distinct mutations in the beta-myosin heavy chain gene. A 908Leu----Val mutation and a 403Arg----Gln mutation

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Familial hypertrophic cardiomyopathy. Microsatellite haplotyping and identification of a hot spot for mutations in the beta-myosin heavy chain gene

1 reference

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

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Early expression of a malignant phenotype of familial hypertrophic cardiomyopathy associated with a Gly716Arg myosin heavy chain mutation in a Korean family

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Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathy

1 reference

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Hypertrophic cardiomyopathy in children

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Hypertrophic cardiomyopathy--beyond the sarcomere

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Coexistence of mitochondrial DNA and beta myosin heavy chain mutations in hypertrophic cardiomyopathy with late congestive heart failure

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Detection of numerous Y chromosome biallelic polymorphisms by denaturing high-performance liquid chromatography

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A novel mutation in KVLQT1 is the molecular basis of inherited long QT syndrome in a near-drowning patient's family.

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Ion channels--basic science and clinical disease

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Genotype-phenotype correlations in hypertrophic cardiomyopathy. Insights provided by comparisons of kindreds with distinct and identical beta-myosin heavy chain gene mutations

1 reference

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Hypertrophic cardiomyopathy: histopathological features of sudden death in cardiac troponin T disease

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Identifiers

10.1016/S0735-1097(02)01900-9

1 reference

Europe PubMed Central

6 February 2018

http://europepmc.org/abstract/MED/12084606

1 reference

Europe PubMed Central

6 February 2018

http://europepmc.org/abstract/MED/12084606

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