Hypertrophic cardiomyopathy: the genetic determinants of clinical disease expression (Q37070209)

18 August 2017

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title

Hypertrophic cardiomyopathy: the genetic determinants of clinical disease expression (English)

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hypertrophic cardiomyopathy

18 August 2017

main subject

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Andre Keren

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18 August 2017

Petros Syrris

series ordinal

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18 August 2017

William J McKenna

series ordinal

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18 August 2017

publication date

29 January 2008

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Nature Clinical Practice Cardiovascular Medicine

18 August 2017

published in

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18 August 2017

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18 August 2017

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18 August 2017

page(s)

158-168

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Report of the 1995 World Health Organization/International Society and Federation of Cardiology Task Force on the Definition and Classification of cardiomyopathies.

18 August 2017

cites work

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

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

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Identification of a metavinculin missense mutation, R975W, associated with both hypertrophic and dilated cardiomyopathy

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A mutation in the human phospholamban gene, deleting arginine 14, results in lethal, hereditary cardiomyopathy.

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

Gender and aging in a transgenic mouse model of hypertrophic cardiomyopathy

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7 January 2021

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7 January 2021

Angiotensin-I Converting Enzyme Genotypes and Left Ventricular Hypertrophy in Patients With Hypertrophic Cardiomyopathy

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7 January 2021

The influence of the angiotensin I converting enzyme genotype in familial hypertrophic cardiomyopathy varies with the disease gene mutation

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7 January 2021

Genetic polymorphisms in the renin-angiotensin-aldosterone system associated with expression of left ventricular hypertrophy in hypertrophic cardiomyopathy: a study of five polymorphic genes in a family with a disease causing mutation in the myosin

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7 January 2021

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

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7 January 2021

Occurrence and significance of progressive left ventricular wall thinning and relative cavity dilatation in hypertrophic cardiomyopathy

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7 January 2021

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7 January 2021

Prevalence, clinical profile, and significance of left ventricular remodeling in the end-stage phase of hypertrophic cardiomyopathy

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7 January 2021

Novel mutation in the alpha-tropomyosin gene and transition from hypertrophic to hypocontractile dilated cardiomyopathy.

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7 January 2021

Phenotypic diversity in hypertrophic cardiomyopathy

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7 January 2021

Echocardiography-guided genetic testing in hypertrophic cardiomyopathy: septal morphological features predict the presence of myofilament mutations

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7 January 2021

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7 January 2021

Identifiers

DOI

10.1038/NCPCARDIO1110

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Dimensions Publication ID

18 August 2017

1047628611

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