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Volumn 49, Issue 1, 2001, Pages 125-129

Variable phenotype of Alzheimer's disease with spastic paraparesis

Author keywords

[No Author keywords available]

Indexed keywords

AMYLOID BETA PROTEIN; PRESENILIN 1;

EID: 0035115610     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/1531-8249(200101)49:1<125::AID-ANA21>3.0.CO;2-1     Document Type: Article
Times cited : (84)

References (20)
  • 2
    • 8244260610 scopus 로고    scopus 로고
    • Two novel (M233T and R278T) presenilin-1 mutations in early-onset Alzheimer's disease and preliminary evidence for association of presenilin-1 mutations with a novel phenotype
    • (1997) Neuroreport , vol.8 , pp. 1537-1542
    • Kwok, J.B.J.1    Taddei, K.2    Hallupp, M.3
  • 13
    • 0025908356 scopus 로고
    • The Consortium to Establish a Registry for Alzheimer's Disease (CERAD). Part II. Standardization of the neuropathologic assessment of Alzheimer's disease
    • (1991) Neurology , vol.41 , pp. 479-486
    • Mirra, S.S.1    Heyman, A.2    McKeel, D.3
  • 14
    • 0032511186 scopus 로고    scopus 로고
    • Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease
    • (1998) Cell , vol.93 , pp. 973-983
    • Casari, G.1    De Fusco, M.2    Ciarmatori, S.3
  • 16
    • 0034076439 scopus 로고    scopus 로고
    • Identification of a novel 4.6-kb genomic deletion in presenilin-1 gene which resuits in exclusion of exon 9 in a Finnish early onset Alzheimer's disease family: An Alu core sequence-stimulated recombination?
    • (2000) Eur J Hum Genet , vol.8 , pp. 259-266
    • Hiltunen, M.1    Helisalmi, S.2    Mannermaa, A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.