(Q33936341)

30 July 2017

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title

Prevalence and characteristics of dystrophin defects in adult male patients with dilated cardiomyopathy (English)

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30 July 2017

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dilated cardiomyopathy

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Arbustini E

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30 July 2017

Diegoli M

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30 July 2017

Morbini P

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30 July 2017

Dal Bello B

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30 July 2017

Banchieri N

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30 July 2017

Pilotto A

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30 July 2017

Magani F

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30 July 2017

Grasso M

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30 July 2017

Narula J

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30 July 2017

Gavazzi A

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30 July 2017

Viganò M

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30 July 2017

Tavazzi L

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30 July 2017

language of work or name

English

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publication date

1 June 2000

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Journal of the American College of Cardiology

30 July 2017

published in

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30 July 2017

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30 July 2017

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30 July 2017

page(s)

1760-1768

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X-linked dilated cardiomyopathy

30 July 2017

cites work

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https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900650-1

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

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900650-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900650-1

7 January 2021

X-linked dilated cardiomyopathy. Novel mutation of the dystrophin gene

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900650-1

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

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900650-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900650-1

7 January 2021

Insertional mutation by transposable element, L1, in the DMD gene results in X-linked dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900650-1

7 January 2021

A novel Alu-like element rearranged in the dystrophin gene causes a splicing mutation in a family with X-linked dilated cardiomyopathy.

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900650-1

7 January 2021

Dystrophin gene abnormalities in two patients with idiopathic dilated cardiomyopathy.

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900650-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900650-1

7 January 2021

Dilating cardiomyopathy as the expression of Xp21 Becker type muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900650-1

7 January 2021

Dilated cardiomyopathy requiring cardiac transplantation as initial manifestation of Xp21 Becker type muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900650-1

7 January 2021

Duchenne dystrophy: Electron microscopic findings pointing to a basic or early abnormality in the plasma membrane of the muscle fiber

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900650-1

7 January 2021

Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900650-1

7 January 2021

Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900650-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900650-1

7 January 2021

Restrictive Cardiomyopathy, Atrioventricular Block and Mild to Subclinical Myopathy in Patients With Desmin-Immunoreactive Material Deposits

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https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900650-1

7 January 2021

Mitochondrial DNA mutations and mitochondrial abnormalities in dilated cardiomyopathy

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https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900650-1

7 January 2021

Enteroviral RNA and virus-like particles in the skeletal muscle of patients with idiopathic dilated cardiomyopathy

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https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900650-1

7 January 2021

Cardiac immunocyte-derived (AL) amyloidosis: an endomyocardial biopsy study in 11 patients.

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900650-1

7 January 2021

H and L ferritins in myocardium in iron overload

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900650-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900650-1

7 January 2021

An informative polymorphism detectable by polymerase chain reaction at the 3' end of the dystrophin gene

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900650-1

7 January 2021

Two polymorphic dinucleotide repeats in intron 44 of the dystrophin gene

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900650-1

7 January 2021

Mutation of dystrophin gene and cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900650-1

7 January 2021

Myocardial involvement is very frequent among patients affected with subclinical Becker's muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900650-1

7 January 2021

Restoration of half the normal dystrophin sequence in a double-deletion Duchenne muscular dystrophy family

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900650-1

7 January 2021

Heart failure-related myopathy. Clinical and pathophysiological insights

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900650-1

7 January 2021

The heart in limb girdle muscular dystrophy.

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900650-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900650-1

7 January 2021

10.1016/S0735-1097(00)00650-1

Identifiers

DOI

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30 July 2017

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