42nd ENMC Sponsored International Workshop: X-linked cardiomyopathies. 21-23 June 1996, Naarden, The Netherlands (Q73778905)

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6 November 2019

title

42nd ENMC Sponsored International Workshop: X-linked cardiomyopathies. 21-23 June 1996, Naarden, The Netherlands (English)

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6 November 2019

author name string

G Nigro

series ordinal

1

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6 November 2019

F Muntoni

series ordinal

2

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6 November 2019

publication date

1 September 1997

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6 November 2019

published in

Neuromuscular Disorders

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6 November 2019

volume

7

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6 November 2019

issue

6-7

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6 November 2019

page(s)

397-403

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Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

6 November 2019

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Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy

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Novel small mutations along the DMD/BMD gene associated with different phenotypes

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SSCP detection of novel mutations in patients with Emery-Dreifuss muscular dystrophy: definition of a small C-terminal region required for emerin function

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

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A gene mutated in X-linked myotubular myopathy defines a new putative tyrosine phosphatase family conserved in yeast

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Isolation of the gene for McLeod syndrome that encodes a novel membrane transport protein

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Atypical McLeod syndrome manifested as X-linked chorea-acanthocytosis, neuromyopathy and dilated cardiomyopathy: report of a family

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Familial cardiomyopathy, mental retardation and myopathy associated with desmin-type intermediate filaments

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Sarcolemmal indentation in cardiomyopathy with mental retardation and vacuolar myopathy

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Cardiac involvement in Becker muscular dystrophy.

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Dilated Cardiomyopathy of Muscular Dystrophy: A Multifaceted Approach to Management

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The incidence and evolution of cardiomyopathy in Duchenne muscular dystrophy

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Evaluation of the cardiomyopathy in becker muscular dystrophy

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Development of cardiomyopathy in female carriers of Duchenne and Becker muscular dystrophies

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

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

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Molecular analysis of the Duchenne muscular dystrophy gene in patients with Becker muscular dystrophy presenting with dilated cardiomyopathy

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

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

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Becker muscular dystrophy: detection of unusual disease courses by combined approach to dystrophin analysis

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Dilated cardiomyopathy and the dystrophin gene: an illustrated review

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

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7 January 2021

Mutation of dystrophin gene and cardiomyopathy

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7 January 2021

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Identification of a novel sarcoglycan gene at 5q33 encoding a sarcolemmal 35 kDa glycoprotein

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7 January 2021

Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene

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Identification of the Syrian hamster cardiomyopathy gene.

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

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7 January 2021

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7 January 2021

Sudden death of a carrier of X-linked Emery-Dreifuss muscular dystrophy

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7 January 2021

Cardiac transplantation in female Emery-Dreifuss muscular dystrophy

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7 January 2021

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7 January 2021

Follow up study of cardiac involvement in Emery-Dreifuss muscular dystrophy

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Emery-Dreifuss muscular dystrophy. An autopsy case

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Emerin deficiency at the nuclear membrane in patients with Emery-Dreifuss muscular dystrophy

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7 January 2021

Diagnosis of X-linked Emery-Dreifuss muscular dystrophy by protein analysis of leucocytes and skin with monoclonal antibodies

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7 January 2021

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Identifiers

DOI

1 reference

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6 November 2019

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