(Q74799061)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9673984%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

review article

1 reference

title

Overview of distal myopathies: from the clinical to the molecular (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9673984%20AND%20SRC:MED&resulttype=core&format=json

distal muscular dystrophy

13 November 2019

main subject

1 reference

R J Barohn

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9673984%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

A A Amato

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9673984%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

R C Griggs

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9673984%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

publication date

1 June 1998

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9673984%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

published in

Neuromuscular Disorders

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9673984%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

volume

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9673984%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9673984%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

page(s)

309-316

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9673984%20AND%20SRC:MED&resulttype=core&format=json

Distal myopathies and dystrophies

13 November 2019

cites work

1 reference

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7 January 2021

Sensory involvement in distal myopathy (Welander)

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7 January 2021

Myopathia distalis tarda hereditaria

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7 January 2021

Late distal myopathy. Report of a case

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7 January 2021

Intranuclear and cytoplasmic filamentous inclusions in distal myopathy (Welander)

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7 January 2021

Inclusion body myositis and welander distal myopathy: a clinical, neurophysiological and morphological comparison

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7 January 2021

Welander's distal myopathy: clinical, neurophysiological and muscle biopsy observations in young and middle aged adults with early symptoms

1 reference

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7 January 2021

Histochemical and histopathological changes in skeletal muscle in late-onset hereditary distal myopathy (Welander)

1 reference

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7 January 2021

Neurogenic involvement in distal myopathy (Welander). Histochemical and morphological observations on muscle and nerve biopsies

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7 January 2021

Inclusion body myositis and myopathies

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7 January 2021

Idiopathic inflammatory myopathies

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7 January 2021

Welander distal myopathy is not linked to other defined distal myopathy gene loci

1 reference

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7 January 2021

Distal muscular dystrophy in an English family

1 reference

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7 January 2021

Late onset hereditary distal myopathy

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7 January 2021

Muscular dystrophy with separate clinical phenotypes in a large family

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7 January 2021

Tibial muscular dystrophy. Late adult-onset distal myopathy in 66 Finnish patients

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7 January 2021

Late onset foot-drop muscular dystrophy with rimmed vacuoles

1 reference

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7 January 2021

Familial distal myopathy with rimmed vacuole and lamellar (myeloid) body formation

1 reference

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7 January 2021

Autosomal recessive distal muscular dystrophy: a comparative study with distal myopathy with rimmed vacuole formation

1 reference

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7 January 2021

Distal myopathy with rimmed vacuole formation. A follow-up study

1 reference

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7 January 2021

Distal myopathy: Electron microscopic and histochemical studies

1 reference

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7 January 2021

Sporadic distal myopathy with early adult onset

1 reference

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7 January 2021

Distal Vacuolar Myopathy With Complete Heart Block

1 reference

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7 January 2021

Autosomal recessive distal myopathy

1 reference

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7 January 2021

Distal muscular dystrophy with autosomal recessive inheritance

1 reference

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7 January 2021

Distal myopathies. 25th ENMC International Workshop, 18-20 November 1994, Naarden, The Netherlands.

1 reference

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7 January 2021

On the classification, natural history and treatment of the myopathies

1 reference

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7 January 2021

Rimmed vacuolar distal myopathy: a clinical, electrophysiological, histopathological and computed tomographic study of seven cases

1 reference

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7 January 2021

Vacuolar myopathy sparing the quadriceps

1 reference

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7 January 2021

The spectrum of familial inclusion body myopathies in 13 families and a description of a quadriceps-sparing phenotype in non-Iranian Jews

1 reference

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7 January 2021

"Rimmed vacuole myopathy" sparing the quadriceps. A unique disorder in Iranian Jews

1 reference

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7 January 2021

Familial inclusion body myositis among Kurdish-Iranian Jews

1 reference

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7 January 2021

Hereditary distal myopathy with filamentous inclusions

1 reference

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7 January 2021

Rimmed vacuolar distal myopathy. An ultrastructural study

1 reference

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7 January 2021

Rimmed basophilic vacuoles and filamentous inclusions in neuromuscular disorders

1 reference

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7 January 2021

Inclusion body myositis: clinical and pathological boundaries

1 reference

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7 January 2021

New developments in hereditary inclusion body myopathies

1 reference

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7 January 2021

Gene locus for autosomal recessive distal myopathy with rimmed vacuoles maps to chromosome 9

1 reference

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7 January 2021

Various types of hereditary inclusion body myopathies map to chromosome 9p1-q1

1 reference

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7 January 2021

Autosomal recessive distal muscular dystrophy as a new type of progressive muscular dystrophy. Seventeen cases in eight families including an autopsied case

1 reference

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7 January 2021

A new type of distal myopathy in two brothers

1 reference

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7 January 2021

High serum levels of creatine kinase: asymptomatic prelude to distal myopathy

1 reference

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7 January 2021

Autosomal recessive distal dystrophy

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7 January 2021

Computerized tomography and magnetic resonance muscle imaging in Miyoshi's myopathy

1 reference

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7 January 2021

Miyoshi-type distal muscular dystrophy. Clinical spectrum in 24 Dutch patients

1 reference

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7 January 2021

Autosomal recessive distal muscular dystrophy: normal expression of dystrophin, utrophin and dystrophin-associated proteins in muscle fibers

1 reference

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7 January 2021

Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14

1 reference

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7 January 2021

A gene for autosomal recessive limb-girdle muscular dystrophy maps to chromosome 2p

1 reference

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7 January 2021

Clinical and molecular analysis of a large family with three distinct phenotypes of progressive muscular dystrophy.

1 reference

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7 January 2021

Desmin-related neuromuscular disorders

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

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7 January 2021

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

1 reference

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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%2900030-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900030-3

7 January 2021

Autosomal dominant ?spheroid body myopathy?

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900030-3

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%2900030-3

7 January 2021

Mallory body-like inclusions in a hereditary congenital neuromuscular disease

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900030-3

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%2900030-3

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%2900030-3

7 January 2021

Chromosome 12-linked autosomal dominant scapuloperoneal muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900030-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900030-3

7 January 2021

Vimentin and desmin in maturing skeletal muscle and developmental myopathies

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900030-3

7 January 2021

Hereditary Distal Myopathy With Onset in Infancy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900030-3

7 January 2021

Distal myopathy with onset in early infancy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900030-3

7 January 2021

Hereditary distal myopathy with onset in early infancy. Observation of a family

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900030-3

7 January 2021

Assignment of the tibial muscular dystrophy locus to chromosome 2q31.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900030-3

7 January 2021

10.1016/S0960-8966(98)00030-3

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9673984%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

1 reference