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Volumn 47, Issue 4 SUPPL., 1996, Pages 1106-1107

Nine families with the SCA3/Machado-Joseph disease type of inherited ataxia

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT DISORDER; CLINICAL ARTICLE; DIFFERENTIAL DIAGNOSIS; ETHNIC GROUP; HEREDITARY ATAXIA; HIGH RISK POPULATION; HUMAN; HUMAN CELL; HUMAN TISSUE; MACHADO JOSEPH DISEASE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SPINOCEREBELLAR TRACT;

EID: 0029808638     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.47.4.1106-a     Document Type: Article
Times cited : (2)

References (7)
  • 1
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    • Mutations in American families with spinocerebellar ataxia (SCA) type 3: SCA3 is allelic to MachadoJoscph disease
    • Higgins JJ, Nee LE, Vasconcelos O, et al. Mutations in American families with spinocerebellar ataxia (SCA) type 3: SCA3 is allelic to MachadoJoscph disease. Neurology 1996;46:208-213.
    • (1996) Neurology , vol.46 , pp. 208-213
    • Higgins, J.J.1    Nee, L.E.2    Vasconcelos, O.3
  • 2
    • 9344245162 scopus 로고    scopus 로고
    • Frequency of spinocerebellar ataxia type 1, dentatorubropallidoluysian atrophy, and Machado-Joseph disease mutations in a large group of spinocerebellar ataxia patients
    • Silveira I, Lopes-Cendes I, Kish S, et al. Frequency of spinocerebellar ataxia type 1, dentatorubropallidoluysian atrophy, and Machado-Joseph disease mutations in a large group of spinocerebellar ataxia patients. Neurology 1996;46:214-218.
    • (1996) Neurology , vol.46 , pp. 214-218
    • Silveira, I.1    Lopes-Cendes, I.2    Kish, S.3
  • 3
    • 0029134871 scopus 로고
    • Spinocerebellar ataxia type 1 and Machado-Joseph disease: Incidence of CAG expansions among adult-onset ataxia patients from 311 families with dominant, recessive or sporadic ataxia
    • Ranum LPW, Lundgren JK, Schut LJ, et al. Spinocerebellar ataxia type 1 and Machado-Joseph disease: incidence of CAG expansions among adult-onset ataxia patients from 311 families with dominant, recessive or sporadic ataxia. Am J Hum Genet 1995;57:603-608.
    • (1995) Am J Hum Genet , vol.57 , pp. 603-608
    • Lpw, R.1    Lundgren, J.K.2    Schut, L.J.3
  • 4
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    • Nigro-spino-dentatal degeneration with nuclear ophthalmoplegia
    • Woods BT, Schaumburg HH. Nigro-spino-dentatal degeneration with nuclear ophthalmoplegia. J Neurol Sci 1972;17:149-166.
    • (1972) J Neurol Sci , vol.17 , pp. 149-166
    • Woods, B.T.1    Schaumburg, H.H.2
  • 5
    • 0025118661 scopus 로고
    • Family with dominantly inherited ataxia, amyotrophy, and peripheral sensory loss
    • Eto K, Sumi SM, Bird TD, et al. Family with dominantly inherited ataxia, amyotrophy, and peripheral sensory loss. Arch Neurol 1990;47: 968-974.
    • (1990) Arch Neurol , vol.47 , pp. 968-974
    • Eto, K.1    Sumi, S.M.2    Bird, T.D.3
  • 6
    • 0027982415 scopus 로고
    • Megaesophagus and hereditary nervous system degeneration
    • Longstreth GF, Walker FD. Megaesophagus and hereditary nervous system degeneration. J Clin Gastroenterol 1994;19:125-127.
    • (1994) J Clin Gastroenterol , vol.19 , pp. 125-127
    • Longstreth, G.F.1    Walker, F.D.2
  • 7
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    • Severe and prolonged dysphagia complicating botulinum toxin A injections for dystonia in Machado-Joseph disease
    • Tuite PJ, Lang AE. Severe and prolonged dysphagia complicating botulinum toxin A injections for dystonia in Machado-Joseph disease. Neurology 1996;46:846.
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    • Tuite, P.J.1    Lang, A.E.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.