Autosomal dominant hyaline body myopathy presenting as scapuloperoneal syndrome: Clinical features and muscle pathology

Neurology

Volumn 48, Issue 1, 1997, Pages 253-257

  Masuzugawa, S ^a   Kuzuhara, S ^a   Narita, Y ^a   Naito, Y ^a   Taniguchi, A ^a   Ibi, T ^b  

^a MIE UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATASE; HYALIN; MYOSIN HEAVY CHAIN;

ADOLESCENT; ADULT; AGED; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CELL ULTRASTRUCTURE; CLINICAL ARTICLE; CLINICAL FEATURE; FEMALE; HEREDITARY SPINAL MUSCULAR ATROPHY; HISTOPATHOLOGY; HUMAN; IMMUNOHISTOCHEMISTRY; MALE; MUSCLE ATROPHY; MUSCLE BIOPSY; MUSCLE WEAKNESS; ONSET AGE; PATHOGENESIS; PEDIGREE ANALYSIS; PRIORITY JOURNAL;

EID: 0031029620     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.48.1.253     Document Type: Article

References (8)

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3. Barohn RJ, Brumback RA, Mendell JR. Hyaline body myopathy. Neuromuscul Disord 1994;4:257-262.
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8. Wilhelmsen KC, Blake DM, Lynch T, et al. Chromosome 12-linked autosomal dominant scapuloperoneal muscular dystrophy. Ann Neurol 1996;39:507-520.