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Volumn 87, Issue 12, 2004, Pages 1518-1521

Oculopharyngodistal myopathy in a Thai family

Author keywords

Oculopharyngodistal myopathy; Thai family

Indexed keywords

ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; CLINICAL FEATURE; DYSPHAGIA; ETHNIC GROUP; HUMAN; JAPAN; MALE; MUSCLE WEAKNESS; OCULOPHARYNGEAL MUSCULAR DYSTROPHY; OCULOPHARYNGODISTAL MYOPATHY; OPHTHALMOPLEGIA; PTOSIS; THAILAND;

EID: 13744250524     PISSN: 01252208     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (15)

References (10)
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  • 2
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  • 3
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    • An autosomal locus predisposing to deletions of mitochodrial DNA
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    • (1995) Nat Genet , vol.9 , pp. 146-151
    • Suomalainen, A.1    Kaukonen, J.2    Amati, P.3
  • 4
    • 0017327397 scopus 로고
    • Oculopharyngodistal myopathy: Report of four families
    • Satoyoshi E, Kinoshita M. Oculopharyngodistal myopathy: report of four families. Arch Neurol 1977; 34: 89-92.
    • (1977) Arch Neurol , vol.34 , pp. 89-92
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  • 5
    • 17344371397 scopus 로고    scopus 로고
    • Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy
    • Brais B, Bouchard J-P, Xie Y-G, et al. Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy. Nat Genet 1998; 180: 164-7.
    • (1998) Nat Genet , vol.180 , pp. 164-167
    • Brais, B.1    Bouchard, J.-P.2    Xie, Y.-G.3
  • 6
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    • Autosomal recessive oculopharyngodistal myopathy in light of distal myopathy with rimmed vacuoles and oculopharyngeal muscular dystrophy
    • Uyama E, Uchino M, Chateau D, et al. Autosomal recessive oculopharyngodistal myopathy in light of distal myopathy with rimmed vacuoles and oculopharyngeal muscular dystrophy. Neuromusc Disord 1998; 8: 119-25.
    • (1998) Neuromusc Disord , vol.8 , pp. 119-125
    • Uyama, E.1    Uchino, M.2    Chateau, D.3
  • 7
    • 0034817325 scopus 로고    scopus 로고
    • Oculopharyngodistal myopathy is genetically heterogeneous and most cases are distinct from oculopharyngeal muscular dystrophy
    • Minami N, Ikezoe K, Kuroda H, et al. Oculopharyngodistal myopathy is genetically heterogeneous and most cases are distinct from oculopharyngeal muscular dystrophy. Neuromusc Disord 2001; 11: 699-702.
    • (2001) Neuromusc Disord , vol.11 , pp. 699-702
    • Minami, N.1    Ikezoe, K.2    Kuroda, H.3
  • 8
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    • Vita, G.1    Dattola, R.2    Santoro, M.3
  • 9
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    • Oculopharyngeal muscular dystrophy
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  • 10
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    • Neuropathic findings in oculopharyngeal muscular dystrophy: A report of seven cases and a review of the literature
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    • Hardiman, O.1    Halperin, J.J.2    Farrell, M.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.