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Volumn 48, Issue 4, 1997, Pages 1118-1120

A presenilin-1 mutation in a Japanese family with Alzheimer's disease and distinctive abnormalities on cranial MRI

Author keywords

[No Author keywords available]

Indexed keywords

AMYLOID PRECURSOR PROTEIN;

EID: 0030944034     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.48.4.1118     Document Type: Article
Times cited : (23)

References (10)
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    • Sherrington, R.1    Rogaev, E.I.2    Liang, Y.3
  • 2
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    • Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene
    • Rogaev EI, Sherrington R, Rovaeva EA, et al. Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene. Nature 1995;376:775-778.
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    • Rogaev, E.I.1    Sherrington, R.2    Rovaeva, E.A.3
  • 3
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    • An increased percentage of long amyloid β protein secreted by familial amyloid β protein precursor (βAPP717) mutants
    • Suzuki N, Cheung TT, Cai XD, et al. An increased percentage of long amyloid β protein secreted by familial amyloid β protein precursor (βAPP717) mutants. Science 1994;264:1336-1340.
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    • Suzuki, N.1    Cheung, T.T.2    Cai, X.D.3
  • 4
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    • Tau in cerebrospinal fluid: A potential diagnostic marker in Alzheimer's disease
    • Arai H, Terajima M, Miura M, et al. Tau in cerebrospinal fluid: a potential diagnostic marker in Alzheimer's disease. Ann Neurol 1995;38:649-652.
    • (1995) Ann Neurol , vol.38 , pp. 649-652
    • Arai, H.1    Terajima, M.2    Miura, M.3
  • 5
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    • Familial amyotrophic lateral sclerosis (ALS) in Japan associated with H46R mutation in Cu/Zn superoxide dismutase gene: A possible new subtype of familial ALS
    • Aoki M, Ogasawara M, Matsubara Y, et al. Familial amyotrophic lateral sclerosis (ALS) in Japan associated with H46R mutation in Cu/Zn superoxide dismutase gene: a possible new subtype of familial ALS. J Neurol Sci 1994;126:77-83.
    • (1994) J Neurol Sci , vol.126 , pp. 77-83
    • Aoki, M.1    Ogasawara, M.2    Matsubara, Y.3
  • 6
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    • Phenotype of chromosome 14-linked familial Alzheimer's disease in a large kindred
    • Lampe TH, Bird TD, Nochlin D, et al. Phenotype of chromosome 14-linked familial Alzheimer's disease in a large kindred. Ann Neurol 1994;36:368-378.
    • (1994) Ann Neurol , vol.36 , pp. 368-378
    • Lampe, T.H.1    Bird, T.D.2    Nochlin, D.3
  • 7
    • 0028952491 scopus 로고
    • Tau in cerebrospinal fluids: Establishment of sandwich ELISA antibody specific to the repeat sequence in tau
    • Mori H, Hosoda K, Matsubara E, et al. Tau in cerebrospinal fluids: establishment of sandwich ELISA antibody specific to the repeat sequence in tau. Neurosci Lett 1995;186:181-183.
    • (1995) Neurosci Lett , vol.186 , pp. 181-183
    • Mori, H.1    Hosoda, K.2    Matsubara, E.3
  • 8
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    • White matter lesions on magnetic resonance imaging in clinically diagnosed Alzheimer's disease
    • Scheltens PH, Barkhof F, Valk J, et al. White matter lesions on magnetic resonance imaging in clinically diagnosed Alzheimer's disease. Brain 1992;115:735-748.
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    • Scheltens, P.H.1    Barkhof, F.2    Valk, J.3
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    • White matter lesions and cognitive deterioration in presymptomatic carriers of the amyloid precursor protein gene codon 693 mutation
    • Bornebroek M, Haan J, van Buchem MA, et al. White matter lesions and cognitive deterioration in presymptomatic carriers of the amyloid precursor protein gene codon 693 mutation. Arch Neurol 1996;53:43-48.
    • (1996) Arch Neurol , vol.53 , pp. 43-48
    • Bornebroek, M.1    Haan, J.2    Van Buchem, M.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.