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Volumn 32, Issue 2, 2005, Pages 253-256

Hyaline body myopathy: Adulthood manifestations

Author keywords

[No Author keywords available]

Indexed keywords

CREATINE KINASE; MYOSIN HEAVY CHAIN;

EID: 20544458097     PISSN: 03171671     EISSN: None     Source Type: Journal    
DOI: 10.1017/S0317167100004078     Document Type: Article
Times cited : (8)

References (13)
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    • (1994) Myology. 2nd Ed. , pp. 939-944
    • Engel, A.G.1    Banker, B.Q.2
  • 3
    • 0017356724 scopus 로고
    • A new congenital myopathy: A morphological, cytochemical and histochemical study
    • Sahgal V, Sahgal S. A new congenital myopathy: a morphological, cytochemical and histochemical study. Acta Neuropathol (Berl) 1977;37:225-230.
    • (1977) Acta Neuropathol (Berl) , vol.37 , pp. 225-230
    • Sahgal, V.1    Sahgal, S.2
  • 5
    • 0027288603 scopus 로고
    • Hyaline bodies in skeletal muscle of a patient with a mild chronic nonprogressive congenital myopathy
    • Ceuterick C, Martin JJ, Martens C. Hyaline bodies in skeletal muscle of a patient with a mild chronic nonprogressive congenital myopathy. Clin Neuropathol 1993;12:79-83.
    • (1993) Clin Neuropathol , vol.12 , pp. 79-83
    • Ceuterick, C.1    Martin, J.J.2    Martens, C.3
  • 6
    • 0031029620 scopus 로고    scopus 로고
    • Autosomal dominant hyaline body myopathy presenting as scapuloperoneal syndrome: Clinical features and muscle pathology
    • Masuzugawa S, Kuzuhara S, Narita Y, et al. Autosomal dominant hyaline body myopathy presenting as scapuloperoneal syndrome: clinical features and muscle pathology. Neurology 1997;48:253-257.
    • (1997) Neurology , vol.48 , pp. 253-257
    • Masuzugawa, S.1    Kuzuhara, S.2    Narita, Y.3
  • 7
    • 0344738673 scopus 로고    scopus 로고
    • Autosomal dominant hyaline body myopathy: Clinical variability and pathologic findings
    • Bohlega S, Lach B, Meyer BF, et al. Autosomal dominant hyaline body myopathy: clinical variability and pathologic findings. Neurology 2003;61:1519-1523.
    • (2003) Neurology , vol.61 , pp. 1519-1523
    • Bohlega, S.1    Lach, B.2    Meyer, B.F.3
  • 8
    • 0141535360 scopus 로고    scopus 로고
    • Myosin storage myopathy associated with a heterozygous missense mutation in MYH7
    • Tajsharghi H, Thornell LE, Lindberg C, et al. Myosin storage myopathy associated with a heterozygous missense mutation in MYH7. Ann Neurol 2003;54:494-500.
    • (2003) Ann Neurol , vol.54 , pp. 494-500
    • Tajsharghi, H.1    Thornell, L.E.2    Lindberg, C.3
  • 9
    • 17144455726 scopus 로고    scopus 로고
    • Identification of a locus for an autosomal recessive hyaline body myopathy at chromosome 3p22.2-p21.32
    • Onengut S, Ugur SA, Karasoy H, Yuceyar N, Tolun A. Identification of a locus for an autosomal recessive hyaline body myopathy at chromosome 3p22.2-p21.32. Neuromuscul Disord 2004;14:4-9.
    • (2004) Neuromuscul Disord , vol.14 , pp. 4-9
    • Onengut, S.1    Ugur, S.A.2    Karasoy, H.3    Yuceyar, N.4    Tolun, A.5
  • 10
    • 0021795389 scopus 로고
    • Pain measurement: An overview
    • Chapman CR, Casey KL, Dubner R, et al: Pain measurement: an overview. Pain 1985;22:1-31.
    • (1985) Pain , vol.22 , pp. 1-31
    • Chapman, C.R.1    Casey, K.L.2    Dubner, R.3
  • 12
    • 0242272985 scopus 로고    scopus 로고
    • Miscellaneous myopathies: Rare myopathies of childhood
    • Karpati G (Ed). ISN Neuropath. Press, Basel
    • Goebel HH. Miscellaneous myopathies: rare myopathies of childhood. In: Karpati G (Ed). Structural and Molecular Basis of Skeletal Muscle Diseases. ISN Neuropath. Press, Basel, 2002: 287
    • (2002) Structural and Molecular Basis of Skeletal Muscle Diseases , pp. 287
    • Goebel, H.H.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.