(Q28216352)

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The failing heart

scientific article (publication date: 10 January 2002)

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scholarly article

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Europe PubMed Central

The failing heart (English)

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author name string

J A Towbin

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N E Bowles

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publication date

10 January 2002

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415

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227-33

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6868

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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.

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https://api.crossref.org/works/10.1038%2F415227A

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Restrictive Cardiomyopathy

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https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

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Spectrum of clinicopathologic manifestations of arrhythmogenic right ventricular cardiomyopathy/dysplasia: a multicenter study.

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

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Right ventricular cardiomyopathy and sudden death in young people

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https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

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Cardiac arrest and sudden death in competitive athletes with arrhythmogenic right ventricular dysplasia

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https://api.crossref.org/works/10.1038%2F415227A

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Epidemiology of idiopathic dilated and hypertrophic cardiomyopathy. A population-based study in Olmsted County, Minnesota, 1975-1984

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https://api.crossref.org/works/10.1038%2F415227A

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The challenge of cardiomyopathy

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https://api.crossref.org/works/10.1038%2F415227A

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Idiopathic cardiomyopathy in the United States, 1970-1982.

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https://api.crossref.org/works/10.1038%2F415227A

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Frequency and phenotypes of familial dilated cardiomyopathy.

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https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

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Localization of a gene responsible for familial dilated cardiomyopathy to chromosome 1q32.

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https://api.crossref.org/works/10.1038%2F415227A

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Familial dilated cardiomyopathy locus maps to chromosome 2q31.

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https://api.crossref.org/works/10.1038%2F415227A

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Desmin mutation responsible for idiopathic dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

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Disruption of heart sarcoglycan complex and severe cardiomyopathy caused by beta sarcoglycan mutations

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https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

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Mutations in the human delta-sarcoglycan gene in familial and sporadic dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

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Gene mapping of familial autosomal dominant dilated cardiomyopathy to chromosome 10q21-23.

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

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Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

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Mutations that alter the surface charge of alpha-tropomyosin are associated with dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

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Actin mutations in dilated cardiomyopathy, a heritable form of heart failure

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

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Desmin-related myopathies in mice and man.

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https://api.crossref.org/works/10.1038%2F415227A

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Sarcoglycans in muscular dystrophy

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https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

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Both hypertrophic and dilated cardiomyopathies are caused by mutation of the same gene, delta-sarcoglycan, in hamster: an animal model of disrupted dystrophin-associated glycoprotein complex

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

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Disruption of the sarcoglycan-sarcospan complex in vascular smooth muscle: a novel mechanism for cardiomyopathy and muscular dystrophy

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

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A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

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Investigation of a family with autosomal dominant dilated cardiomyopathy defines a novel locus on chromosome 2q14-q22.

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

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Mapping a cardiomyopathy locus to chromosome 3p22-p25.

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

based on heuristic

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Linkage of familial dilated cardiomyopathy with conduction defect and muscular dystrophy to chromosome 6q23.

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

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Neonatal cardiomyopathy in mice homozygous for the Arg403Gln mutation in the alpha cardiac myosin heavy chain gene

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

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Lamin A/C Gene Mutation Associated With Dilated Cardiomyopathy With Variable Skeletal Muscle Involvement

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

based on heuristic

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X-linked dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

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X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

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Brief report: deletion of the dystrophin muscle-promoter region associated with X-linked dilated cardiomyopathy.

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

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Dystrophin: the protein product of the Duchenne muscular dystrophy locus

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

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The association of cardiac dystrophin with myofibrils/Z-disc regions in cardiac muscle suggests a novel role in the contractile apparatus

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

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Distinct patterns of dystrophin organization in myocyte sarcolemma and transverse tubules of normal and diseased human myocardium

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

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Three muscular dystrophies: loss of cytoskeleton-extracellular matrix linkage.

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

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Neuronal nitric oxide synthase and dystrophin-deficient muscular dystrophy

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

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Animal models for muscular dystrophy: valuable tools for the development of therapies

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

based on heuristic

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Cardiomyopathy in animal models of muscular dystrophy

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

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Dystrophin protects the sarcolemma from stresses developed during muscle contraction

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

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The role of cytoskeletal proteins in cardiomyopathies

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

based on heuristic

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The "final common pathway" hypothesis and inherited cardiovascular disease. The role of cytoskeletal proteins in dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

based on heuristic

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An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

based on heuristic

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X-linked dilated cardiomyopathy with neutropenia, growth retardation, and 3-methylglutaconic aciduria

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

based on heuristic

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A novel X-linked gene, G4.5. is responsible for Barth syndrome

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

based on heuristic

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The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathies.

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

based on heuristic

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Neonatal, lethal noncompaction of the left ventricular myocardium is allelic with Barth syndrome

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

based on heuristic

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MLP-deficient mice exhibit a disruption of cardiac cytoarchitectural organization, dilated cardiomyopathy, and heart failure

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

based on heuristic

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Enteroviral protease 2A cleaves dystrophin: evidence of cytoskeletal disruption in an acquired cardiomyopathy.

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

based on heuristic

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Hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

based on heuristic

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Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14q1

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular genetics of hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

based on heuristic

inferred from DOI database lookup

A familial hypertrophic cardiomyopathy locus maps to chromosome 15q2.

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

based on heuristic

inferred from DOI database lookup

Mdx mice inducibly expressing dystrophin provide insights into the potential of gene therapy for duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

based on heuristic

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Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathy

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

based on heuristic

inferred from DOI database lookup

Novel gene mutations in patients with left ventricular noncompaction or Barth syndrome

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

based on heuristic

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Manipulating the contractile apparatus: genetically defined animal models of cardiovascular disease

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

based on heuristic

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A transgenic rabbit model for human hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

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Familial hypertrophic cardiomyopathy in maine coon cats: an animal model of human disease

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

based on heuristic

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Cardiac defects and altered ryanodine receptor function in mice lacking FKBP12

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

based on heuristic

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Role for alpha-dystrobrevin in the pathogenesis of dystrophin-dependent muscular dystrophies

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

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Serum soluble heat shock protein 60 is elevated in subjects with atherosclerosis in a general population

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

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Mechanical circulatory support for advanced heart failure: effect of patient selection on outcome

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

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Prevention of cardiomyopathy in mouse models lacking the smooth muscle sarcoglycan-sarcospan complex

1 reference

https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

based on heuristic

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Sarcoglycan, the heart, and skeletal muscles: new treatment, old drug?

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https://api.crossref.org/works/10.1038%2F415227A

7 January 2021

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Identifiers

10.1038/415227A

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Consolidated OpenCitations Corpus – April 2017

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OpenCitations bibliographic resource ID

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

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Springer Nature article ID

10.1038/415227a

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