(Q48022720)

7 February 2018

title

Familial cardiomyopathy and distal myopathy with abnormal desmin accumulation and migration. (English)

1 reference

7 February 2018

main subject

familial cardiomyopathy

1 reference

distal muscular dystrophy

inferred from title

1 reference

3

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7 February 2018

author name string

Lobrinus JA

1

1 reference

7 February 2018

Janzer RC

2

1 reference

7 February 2018

Matthieu JM

4

1 reference

7 February 2018

Pfend G

5

1 reference

7 February 2018

Goy JJ

6

1 reference

7 February 2018

Bogousslavsky J

7

1 reference

7 February 2018

publication date

1 April 1998

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7 February 2018

published in

Neuromuscular Disorders

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7 February 2018

volume

8

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7 February 2018

issue

2

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7 February 2018

page(s)

77-86

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7 February 2018

Desmin-related neuromuscular disorders

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900005-4

7 January 2021

Myofibrillar myopathy with abnormal foci of desmin positivity. I. Light and electron microscopy analysis of 10 cases

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900005-4

7 January 2021

Peripheral neuropathy with giant axons and cardiomyopathy associated with desmin type intermediate filaments in skeletal muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900005-4

7 January 2021

Neuromyopathy and restrictive cardiomyopathy with accumulation of intermediate filaments: a clinical, morphological and biochemical study.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900005-4

7 January 2021

Hereditary distal myopathy with granulo-filamentous cytoplasmic inclusions containing desmin, dystrophin and vimentin

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900005-4

7 January 2021

Myopathy associated with desmin type intermediate filaments. An immunoelectron microscopic study

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900005-4

7 January 2021

Familial desminopathy: myopathy with accumulation of desmin-type intermediate filaments

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900005-4

7 January 2021

Autosomal dominant distal myopathy with desmin storage: a clinicopathologic and electrophysiologic study of a large kinship

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900005-4

7 January 2021

Desmin myopathy: a multisystem disorder involving skeletal, cardiac, and smooth muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900005-4

7 January 2021

RAPID EXAMINATION OF MUSCLE TISSUE. AN IMPROVED TRICHROME METHOD FOR FRESH-FROZEN BIOPSY SECTIONS

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https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900005-4

7 January 2021

Purification and partial structural and functional characterization of mouse myelin/oligodendrocyte glycoprotein

1 reference

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7 January 2021

A new type of hereditary distal myopathy with characteristic sarcoplasmic bodies and intermediate (skeletin) filaments

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900005-4

7 January 2021

Inclusion Bodies in Human Neuromuscular Disorder

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7 January 2021

Cytoplasmic body neuromyopathy presenting as respiratory failure and weight loss

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900005-4

7 January 2021

Autosomal dominant ?spheroid body myopathy?

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900005-4

7 January 2021

Subsarcolemmal vermiform deposits in skeletal muscle, associated with familial cardiomyopathy: report of two cases of a new entity

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900005-4

7 January 2021

Reducing body myopathy and desmin storage in skeletal muscle: morphological and biochemical findings

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900005-4

7 January 2021

Cytoplasmic body myopathy: familial cases with accumulation of desmin and dystrophin. An immunohistochemical, immunoelectron microscopic and biochemical study

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900005-4

7 January 2021

Nemaline myopathy appearing in adults as cardiomyopathy. A clinicopathologic study

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900005-4

7 January 2021

Congenital nemaline myopathy with dilated cardiomyopathy: an autopsy study

1 reference

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7 January 2021

Alpha-actinin in nemaline bodies in congenital nemaline myopathy: immunological confirmation by light and electron microscopy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900005-4

7 January 2021

Storage of phosphorylated desmin in a familial myopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900005-4

7 January 2021

Familial desmin myopathies and cytoplasmic body myopathies

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900005-4

7 January 2021

Human desmin gene: cDNA sequence, regional localization and exclusion of the locus in a familial desmin-related myopathy.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900005-4

7 January 2021

Cardiovascular lesions and skeletal myopathy in mice lacking desmin.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900005-4

7 January 2021

Familial desmin-related myopathies and cardiomyopathies--from myopathology to molecular and clinical genetics. 36th European Neuromuscular Center (ENMC)-Sponsored International Workshop 20-22 October, 1995, Naarden, The Netherlands

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900005-4

7 January 2021

10.1016/S0960-8966(98)00005-4

Identifiers

DOI

1 reference

7 February 2018

PubMed ID

9608560

1 reference

7 February 2018