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Volumn 24, Issue 11, 2001, Pages 1440-1450

Clinical and genetic aspects of distal myopathies

Author keywords

Distal; Inherited; Muscular dystrophy; Myopathy

Indexed keywords

CLINICAL FEATURE; DISTAL MYOPATHY; GENETIC PREDISPOSITION; HUMAN; MOLECULAR GENETICS; MUSCLE DISEASE; MUSCLE WEAKNESS; PRIORITY JOURNAL; REVIEW;

EID: 0034783436     PISSN: 0148639X     EISSN: None     Source Type: Journal    
DOI: 10.1002/mus.1167     Document Type: Review
Times cited : (29)

References (127)
  • 8
    • 0030891310 scopus 로고    scopus 로고
    • New developments in hereditary inclusion body myopathies
    • (1997) Ann Neurol , vol.41 , pp. 421-422
    • Askanas, V.1
  • 32
    • 0016763981 scopus 로고
    • Histochemical and histopathological changes in skeletal muscle in late-onset hereditary distal myopathy (Welander)
    • (1975) J Neurol Sci , vol.26 , pp. 147-157
    • Edström, L.1
  • 48
  • 49
  • 85
    • 0001283510 scopus 로고
    • Fascioscapulohumeral dystrophy and the scapuloperoneal syndrome
    • Engel AG, Fanzini-Armstrong C, editors. New York: McGraw Hill
    • (1994) Myology , pp. 1220-1232
    • Munsat, T.E.1
  • 98
    • 0026744205 scopus 로고
    • Vimentin and desmin in maturing skeletal muscle and developmental myopathies
    • (1992) Neurology , vol.42 , pp. 1616-1624
    • Sarnat, H.B.1
  • 104
    • 0029826654 scopus 로고    scopus 로고
    • The spectrum of familial inclusion body myopathies in 13 families and a description of a quadriceps-sparing phenotype in non-Iranian Jews
    • (1996) Neurology , vol.47 , pp. 977-984
    • Sivakumar, K.1    Dalakas, M.C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.