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Volumn 68, Issue 11, 2001, Pages 1083-1085

Adhalin deficiency: An unusual cause of muscular dystrophy

Author keywords

Consanguinity; Muscle biopsy; Muscle dystrophy

Indexed keywords

ADHALIN; CYTOSKELETON PROTEIN; MEMBRANE PROTEIN;

EID: 0035515560     PISSN: 00195456     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF02722364     Document Type: Article
Times cited : (6)

References (9)
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    • Kloepfer, H.W.1    Talley, C.2
  • 3
    • 0020606260 scopus 로고
    • Severe childhood muscular dystrophy affecting both sexes and frequent in Tunisia
    • Ben Hamida M, Fardeau M, Attia N. Severe childhood muscular dystrophy affecting both sexes and frequent in Tunisia. Muscle Nerve 1983; 6 : 469-480.
    • (1983) Muscle Nerve , vol.6 , pp. 469-480
    • Ben Hamida, M.1    Fardeau, M.2    Attia, N.3
  • 4
    • 0026757138 scopus 로고
    • Deficiency of the 50K dystrophin-associated glycoprotein in severe childhood autosomal recessive muscular dystrophy
    • Matsumura K, Tome FMS, Collin H, Azibi K, Chaouch M, Kaplar JC et al. Deficiency of the 50K dystrophin-associated glycoprotein in severe childhood autosomal recessive muscular dystrophy. Nature 1992; 359; 320-322.
    • (1992) Nature , vol.359 , pp. 320-322
    • Matsumura, K.1    Tome, F.M.S.2    Collin, H.3    Azibi, K.4    Chaouch, M.5    Kaplar, J.C.6
  • 5
    • 0027484305 scopus 로고
    • Deficiency of the 50 kDa dystrophin associated glycoprotein (adhalin) in severe autosomal recessive muscular dystrophies in children native from European countries
    • Fardeau M, Matsumura K, Tome FMS, Collin H, Leturcq F, Kaplan JC et al. Deficiency of the 50 kDa dystrophin associated glycoprotein (adhalin) in severe autosomal recessive muscular dystrophies in children native from European countries. CR Acad Sci III 1993; 16 : 799-804.
    • (1993) CR Acad Sci III , vol.16 , pp. 799-804
    • Fardeau, M.1    Matsumura, K.2    Tome, F.M.S.3    Collin, H.4    Leturcq, F.5    Kaplan, J.C.6
  • 6
    • 0028226098 scopus 로고
    • Assessment of the 50 kDa dystrophin-associated glycoprotein in Brazilian patients with severe childhood autosomal recessive muscular dystrophy
    • Zatz M, Matsumura K, Vainzof M, Passos-Bueno MR, Pavanello RCM, Marie SK et al. Assessment of the 50 kDa dystrophin-associated glycoprotein in Brazilian patients with severe childhood autosomal recessive muscular dystrophy. J Neurol Sci 1994' 123 : 122-128.
    • (1994) J Neurol Sci , vol.123 , pp. 122-128
    • Zatz, M.1    Matsumura, K.2    Vainzof, M.3    Passos-Bueno, M.R.4    Pavanello, R.C.M.5    Marie, S.K.6
  • 7
    • 0031943778 scopus 로고    scopus 로고
    • From dystrophinopathy to sarcoglycanopathy: Evolution of a concept of muscular dystrophy
    • Ozawa E, Noguchi S, Mizuno Y, Hagiwara Y, Yoshida M. From dystrophinopathy to sarcoglycanopathy: Evolution of a concept of muscular dystrophy. Muscle Nerve 1998; 21 : 421-438.
    • (1998) Muscle Nerve , vol.21 , pp. 421-438
    • Ozawa, E.1    Noguchi, S.2    Mizuno, Y.3    Hagiwara, Y.4    Yoshida, M.5
  • 9


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.