Familial dilated cardiomyopathy (Q59461183)

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9 December 2019

title

Familial dilated cardiomyopathy: evidence for genetic and phenotypic heterogeneity. Heart Muscle Disease Study Group (English)

1 reference

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9 December 2019

main subject

dilated cardiomyopathy

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1

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9 December 2019

Dario Gregori

3

1 reference

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9 December 2019

Gianfranco Sinagra

4

1 reference

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9 December 2019

Mauro Giacca

13

1 reference

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9 December 2019

author name string

C Rocco

2

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9 December 2019

A Di Lenarda

5

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9 December 2019

S Miocic

6

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9 December 2019

M Vatta

7

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9 December 2019

B Pinamonti

8

1 reference

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9 December 2019

F Muntoni

9

1 reference

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9 December 2019

A L Caforio

10

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9 December 2019

W J McKenna

11

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9 December 2019

A Falaschi

12

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9 December 2019

Camerini

14

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9 December 2019

language of work or name

English

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publication date

1 July 1999

1 reference

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Journal of the American College of Cardiology

9 December 2019

published in

1 reference

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9 December 2019

volume

34

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9 December 2019

issue

1

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9 December 2019

page(s)

181-190

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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.

9 December 2019

cites work

1 reference

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7 January 2021

The natural history of idiopathic dilated cardiomyopathy

1 reference

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7 January 2021

Familial aggregation of idiopathic dilated cardiomyopathy

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7 January 2021

Clinical and pathologic study of familial dilated cardiomyopathy

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7 January 2021

The Frequency of Familial Dilated Cardiomyopathy in a Series of Patients with Idiopathic Dilated Cardiomyopathy

1 reference

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7 January 2021

Familial dilated cardiomyopathy in the United Kingdom

1 reference

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7 January 2021

Frequency and phenotypes of familial dilated cardiomyopathy

1 reference

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7 January 2021

Evidence from family studies for autoimmunity in dilated cardiomyopathy

1 reference

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7 January 2021

Recommendations for quantitation of the left ventricle by two-dimensional echocardiography. American Society of Echocardiography Committee on Standards, Subcommittee on Quantitation of Two-Dimensional Echocardiograms

1 reference

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7 January 2021

Prevalence and etiology of idiopathic dilated cardiomyopathy (summary of a National Heart, Lung, and Blood Institute workshop

1 reference

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7 January 2021

Echocardiographic measurements in normal subjects from infancy to old age.

1 reference

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7 January 2021

Idiopathic Dilated Cardiomyopathy

1 reference

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7 January 2021

Nonpredictive value of fibrosis in dilated cardiomyopathy treated with metoprolol

1 reference

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7 January 2021

Dystrophin analysis using a panel of anti-dystrophin antibodies in Duchenne and Becker muscular dystrophy

1 reference

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7 January 2021

A Point Mutation in the 5' Splice Site of the Dystrophin Gene First Intron Responsible for X-Linked Dilated Cardiomyopathy

1 reference

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7 January 2021

Idiopathic dilated cardiomyopathy: lack of association between circulating organ-specific cardiac antibodies and HLA-DR antigens

1 reference

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7 January 2021

The spectrum of left ventricular size in dilated cardiomyopathy: clinical correlates and prognostic implications. SPIC (Italian Multicenter Cardiomyopathy Study) Group

1 reference

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7 January 2021

Mildly dilated congestive cardiomyopathy. Use of prospective diagnostic criteria and description of the clinical course without heart transplantation

1 reference

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7 January 2021

Evolution of a hereditary cardiac conduction and muscle disorder: a study involving a family with six generations affected

1 reference

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7 January 2021

Dystrophin gene abnormalities in two patients with idiopathic dilated cardiomyopathy.

1 reference

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7 January 2021

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

1 reference

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7 January 2021

A mutation in the dystrophin gene selectively affecting dystrophin expression in the heart

1 reference

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7 January 2021

Familial dilated cardiomyopathy: cardiac abnormalities are common in asymptomatic relatives and may represent early disease

1 reference

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7 January 2021

Sporadic hypertrophic cardiomyopathy due to de novo myosin mutations

1 reference

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7 January 2021

Cardiac autoantibodies in dilated cardiomyopathy: a pathogenetic role?

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Mapping a cardiomyopathy locus to chromosome 3p22-p25.

1 reference

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7 January 2021

Cardiac transplantation in an incomplete Kearns-Sayre syndrome with mitochondrial DNA deletion

1 reference

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7 January 2021

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

1 reference

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7 January 2021

The structural and functional diversity of dystrophin

1 reference

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7 January 2021

X-linked dilated cardiomyopathy

1 reference

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7 January 2021

Cardiac involvement in Becker muscular dystrophy.

1 reference

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7 January 2021

Evidence for a dystrophin missense mutation as a cause of X-linked dilated cardiomyopathy.

1 reference

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7 January 2021

A 5' dystrophin duplication mutation causes membrane deficiency of alpha-dystroglycan in a family with X-linked cardiomyopathy

1 reference

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7 January 2021

The 5' region of intron 11 of the dystrophin gene contains target sequences for mobile elements and three overlapping ORFs

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Brief report: deficiency of a dystrophin-associated glycoprotein (adhalin) in a patient with muscular dystrophy and cardiomyopathy

1 reference

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7 January 2021

Dilated cardiomyopathy associated with deficiency of the cytoskeletal protein metavinculin

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Angiotensin-converting enzyme DD genotype in patients with ischaemic or idiopathic dilated cardiomyopathy

1 reference

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7 January 2021

Angiotensinogen gene polymorphism in Japanese patients with hypertrophic cardiomyopathy

1 reference

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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

1 reference

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7 January 2021

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

1 reference

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7 January 2021

Guidelines for the study of familial dilated cardiomyopathies. Collaborative Research Group of the European Human and Capital Mobility Project on Familial Dilated Cardiomyopathy.

1 reference

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7 January 2021

Familial dilated cardiomyopathy: a worse prognosis compared with sporadic forms

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2899%2900172-2

7 January 2021

Familial dilated cardiomyopathy locus maps to chromosome 2q31.

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2899%2900172-2

7 January 2021

10.1016/S0735-1097(99)00172-2

Identifiers

DOI

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9 December 2019

1 reference