(Q47959524)

7 February 2018

review article

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title

Congenital myopathies with inclusion bodies: a brief review. (English)

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7 February 2018

author name string

Goebel HH

series ordinal

1

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7 February 2018

publication date

1 May 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

3-4

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7 February 2018

page(s)

162-168

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7 February 2018

Nonprogressive Congenital Neuromuscular Disease With Uniform Type 1 Fiber

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A new familial congenital myopathy in children with desmin and dystrophin reacting plaques

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Congenital myopathy with excess of thin myofilaments

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Hyaline body myopathy

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Infantile intranuclear rod myopathy

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Nemaline myopathy with intranuclear rods--intranuclear rod myopathy

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The cytoplasmic body: another structural anomaly of the Z disk

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7 January 2021

Desmin and actin associated with cytoplasmic bodies in skeletal muscle fibers: immunocytochemical and fine structural studies, with a note on unusual 18- to 20-nm filaments

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7 January 2021

Induction of spheroid cytoplasmic bodies in a rat muscle by local tetanus

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7 January 2021

The cytoplasmic bodies in a congenital myopathy can be stained with antibodies to desmin, the muscle-specific intermediate filament protein

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7 January 2021

Congenital myopathy with cytoplasmic bodies

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Asymptomatic familial hyperCKemia associated with desmin accumulation in skeletal muscle

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Autosomal dominant ?spheroid body myopathy?

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7 January 2021

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

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Spheroid body myopathy revisited

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Storage of phosphorylated desmin in a familial myopathy

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

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

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7 January 2021

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

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7 January 2021

Unusual familial cardiomyopathy with storage of intermediate filaments in the cardiac muscular cells

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7 January 2021

An unusual familial cardiomyopathy characterized by aberrant accumulations of desmin-type intermediate filaments

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Desmin in myology. 24th European Neuromuscular Center-sponsored workshop held 5-6 November 1993, Naarden, The Netherlands

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7 January 2021

Mallory body-like inclusions in a hereditary congenital neuromuscular disease

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7 January 2021

Congenital myopathy associated with abnormal accumulation of desmin and dystrophin

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7 January 2021

Inclusions in familial cytoplasmic body myopathy are stained by anti-dystrophin antibodies

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7 January 2021

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

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7 January 2021

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

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A dominantly inherited myopathy with excessive tubular aggregates

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7 January 2021

Zebra body myopathy. Clinical, histochemical and ultrastructural studies

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Zebra body myopathy: a second case of ultrastructurally distinct congenital myopathy

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7 January 2021

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

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7 January 2021

Familial Fingerprint Body Myopathy

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7 January 2021

Cylindrical spirals in human skeletal muscle

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7 January 2021

Cylindrical spirals in skeletal muscle: A further observation with clinical, morphological, and biochemical analysis

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7 January 2021

Cylindrical spirals in a familial neuromuscular disorder

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7 January 2021

Autosomal dominant neuromuscular disease with cylindrical spirals

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7 January 2021

10.1016/S0960-8966(98)00022-4

Identifiers

DOI

1 reference

7 February 2018

PubMed ID

9631396

1 reference

7 February 2018