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Neurology
Volumn 51, Issue 2, 1998, Pages 598-600
Inclusion body myositis in twins
Author keywords

[No Author keywords available]
Indexed keywords

ADULT; ARM MUSCLE; ARTICLE; CASE REPORT; HUMAN; HUMAN TISSUE; INCLUSION BODY MYOSITIS; MALE; MUSCLE BIOPSY; MUSCLE WEAKNESS; PRIORITY JOURNAL; QUADRICEPS FEMORIS MUSCLE; TWINS;
EID: 0031781405     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.51.2.598     Document Type: Article
Times cited : (31)
References (10)
  • 1
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  • 2
    • 0029957253 scopus 로고    scopus 로고
    • Inclusion body myositis: Clinical and pathological boundaries
    • Amato AA, Gronseth GS, Jackson CE, et al. Inclusion body myositis: clinical and pathological boundaries. Ann Neurol 1996;40:581-586.
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  • 3
    • 0028787389 scopus 로고
    • Inclusion body myositis and myopathies
    • Griggs RC, Askanas V, DiMauro S, et al. Inclusion body myositis and myopathies. Ann Neurol 1995;38:705-713.
    • (1995) Ann Neurol , vol.38 , pp. 705-713
    • Griggs, R.C.1    Askanas, V.2    DiMauro, S.3
  • 4
    • 0030933296 scopus 로고    scopus 로고
    • Gene locus for autosomal recessive distal myopathy with rimmed vacuoles maps to chromosome 9
    • Ikeuchi T, Asaka T, Saito M, et al. Gene locus for autosomal recessive distal myopathy with rimmed vacuoles maps to chromosome 9. Ann Neurol 1997;41:432-437.
    • (1997) Ann Neurol , vol.41 , pp. 432-437
    • Ikeuchi, T.1    Asaka, T.2    Saito, M.3
  • 5
    • 0030929664 scopus 로고    scopus 로고
    • Hereditary inclusion body myopathy maps to chromosome 9p1-q1
    • Argov Z, Tiram E, Eisenberg I, et al. Hereditary inclusion body myopathy maps to chromosome 9p1-q1. Ann Neurol 1997;41:548-551.
    • (1997) Ann Neurol , vol.41 , pp. 548-551
    • Argov, Z.1    Tiram, E.2    Eisenberg, I.3
  • 6
    • 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
    • Sivakumar K, Dalakas MC. The spectrum of familial inclusion body myopathies in 13 families and a description of a quadriceps-sparing phenotype in non-Iranian Jews. Neurology 1996;47:977-984.
    • (1996) Neurology , vol.47 , pp. 977-984
    • Sivakumar, K.1    Dalakas, M.C.2
  • 7
    • 0028832396 scopus 로고
    • New advances in the understanding of sporadic inclusion body myositis and hereditary inclusion body myopathies
    • Askanas V, Engel WK. New advances in the understanding of sporadic inclusion body myositis and hereditary inclusion body myopathies. Curr Opin Rheumatol 1995;7:486-496.
    • (1995) Curr Opin Rheumatol , vol.7 , pp. 486-496
    • Askanas, V.1    Engel, W.K.2
  • 8
    • 0030891310 scopus 로고    scopus 로고
    • New developments in hereditary inclusion body myopathies
    • Askanas V. New developments in hereditary inclusion body myopathies. Ann Neurol 1997;41:421-422.
    • (1997) Ann Neurol , vol.41 , pp. 421-422
    • Askanas, V.1
  • 9
    • 0022508017 scopus 로고
    • Childhood dermatomyositis in monozygotic twins
    • Harati Y, Niakan E, Bergman EW. Childhood dermatomyositis in monozygotic twins. Neurology 1986;36:721-723.
    • (1986) Neurology , vol.36 , pp. 721-723
    • Harati, Y.1    Niakan, E.2    Bergman, E.W.3
  • 10
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    • An inflammatory, familial, inclusion body myositis with autoimmune features and a phenotype identical to sporadic inclusion body myositis. Studies in three families
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    • Sivakumar, K.1    Semino-Mora, C.2    Dalakas, M.C.3

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.