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Volumn 72, Issue 1, 2002, Pages 43-46

The prevalence of "pure" autosomal dominant hereditary spastic paraparesis in the island of Ireland

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AGED; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHILD; CLINICAL FEATURE; FAMILY; GENE LOCUS; HEALTH SURVEY; HETEROZYGOTE; HUMAN; INFANT; MAJOR CLINICAL STUDY; PREVALENCE; PRIORITY JOURNAL; SPASTIC PARAPLEGIA;

EID: 0036148996     PISSN: 00223050     EISSN: None     Source Type: Journal    
DOI: 10.1136/jnnp.72.1.43     Document Type: Article
Times cited : (52)

References (25)
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  • 3
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    • The hereditary spastic paraplegias
    • (1999) J Neurol , vol.246 , pp. 995-1003
    • Reid, E.1
  • 7
    • 0033868486 scopus 로고    scopus 로고
    • A new locus for autosomal recessive spastic paraplegia associated with mental retardation and distal motor neuropathy, Spg14, maps to chromosome 3q27-q28
    • (2000) Am J Hum Genet , vol.67 , pp. 504-509
    • Vazza, G.1    Zortea, M.2    Baaretto, F.3
  • 13
    • 0034719042 scopus 로고    scopus 로고
    • The phenotype of autosomal dominant hereditary spastic paraparesis due to mutations in the SPAST gene: Comparison with AD-HSP without mutations
    • (2000) Neurology , vol.55 , pp. 1794-1800
    • Mc Monagle, P.1    Byrne, P.2    Fitzgerald, B.3
  • 14
    • 0031976287 scopus 로고    scopus 로고
    • Autosomal dominant hereditary spastic paraparesis with cognitive loss linked to chromosome 2p
    • (1998) Brain , vol.121 , pp. 601-609
    • Webb, S.1    Coleman, D.2    Byrne, P.3
  • 16
    • 0016173785 scopus 로고
    • Hereditary spastic paraplegia in western Norway
    • (1974) Clin Genet , vol.6 , pp. 165-183
    • Skre, H.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.