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Volumn 96, Issue 2, 2012, Pages 281-283

Delayed diagnosis of oculopharyngeal muscular dystrophy in Scotland

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ALLELE; ARTICLE; BILATERAL BROW SUSPENSION; CLINICAL ARTICLE; CRICOPHARYNGEAL MYOTOMY; DELAYED DIAGNOSIS; DYSARTHRIA; DYSPHAGIA; EYE SURGERY; EYELID RECONSTRUCTION; FEMALE; GASTROSTOMY; GENE; HUMAN; LIMB WEAKNESS; LUNDI PROPS; MALE; MOLECULAR DIAGNOSIS; MYOTOMY; NON INVASIVE PROCEDURE; OCULOPHARYNGEAL MUSCULAR DYSTROPHY; ONSET AGE; OPHTHALMOPLEGIA; PABP2 GENE; PHYSIOTHERAPY; PRIORITY JOURNAL; PTOSIS; PTOSIS PROPS; RETROSPECTIVE STUDY; SPEECH THERAPY; UNITED KINGDOM;

EID: 84856025730     PISSN: 00071161     EISSN: 14682079     Source Type: Journal    
DOI: 10.1136/bjo.2010.200378     Document Type: Article
Times cited : (18)

References (11)
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    • Oculopharyngeal muscular dystrophy. A familial disease of late life characterized by dysphagia and progressive ptosis of the evelids
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    • Victor, M.1    Hayes, R.2    Adams, R.D.3
  • 8
    • 0030775367 scopus 로고    scopus 로고
    • Recent studies on oculopharyngeal muscular dystrophy in Que?bec
    • Bouchard JP, Brais B, Brunet D, et al. Recent studies on oculopharyngeal muscular dystrophy in Que?bec. Neuromuscul Disord 1997;(7 Suppl 1):S22-9.
    • (1997) Neuromuscul Disord , Issue.7 SUPPL. 1
    • Bouchard, J.P.1    Brais, B.2    Brunet, D.3
  • 9
    • 59149101614 scopus 로고    scopus 로고
    • Oculopharyngeal muscular dystrophy: A polyalanine myopathy
    • Brais B. Oculopharyngeal muscular dystrophy: a polyalanine myopathy. Curr Neurol Neurosci Rep 2009;9:76-82.
    • (2009) Curr Neurol Neurosci Rep , vol.9 , pp. 76-82
    • Brais, B.1
  • 10
    • 33745940703 scopus 로고    scopus 로고
    • Oculopharyngeal muscular dystrophy: A point mutation which mimics the effect of the PABPN1 gene triplet repeat expansion mutation
    • Robinson DO, Wills AJ, Hammans SR, et al. Oculopharyngeal muscular dystrophy: a point mutation which mimics the effect of the PABPN1 gene triplet repeat expansion mutation. J Med Genet 2006;43:-23.
    • (2006) J Med Genet , vol.43 , pp. 23
    • Robinson, D.O.1    Wills, A.J.2    Hammans, S.R.3
  • 11
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    • Management of myogenic ptosis
    • DOI 10.1016/S0161-6420(02)01009-6, PII S0161642002010096
    • Wong VA, Beckinsale PS, Oley CA, et al. Management of myogenic ptosis. Ophthalmology 2002;109:1023-31. (Pubitemid 34465241)
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    • Wong, V.A.1    Beckingsale, P.S.2    Oley, C.A.3    Sullivan, T.J.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.