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Volumn 229, Issue 3, 1997, Pages 177-180

Analysis of apolipoprotein e, α1-antichymotrypsin and presenilin-1 genes polymorphisms in dementia caused by normal pressure hydrocephalus in man

Author keywords

1 Antichymotrypsin genetics; Apolipoprotein E; Normal pressure hydrocephalus; Polymorphism

Indexed keywords

ALPHA 1 ANTICHYMOTRYPSIN; APOLIPOPROTEIN E; PRESENILIN 1;

EID: 0030742447     PISSN: 03043940     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0304-3940(97)00449-7     Document Type: Article
Times cited : (17)

References (17)
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    • Adams R.D., Fisher C.M., Hakim S., Ojemann R.G., Sweet W.H. Symptomatic occult hydrocephalus with 'normal' cerebrospinal fluid pressure. A treatable syndrome. N. Engl. J. Med. 273:1965;117-126.
    • (1965) N. Engl. J. Med. , vol.273 , pp. 117-126
    • Adams, R.D.1    Fisher, C.M.2    Hakim, S.3    Ojemann, R.G.4    Sweet, W.H.5
  • 4
    • 84965186510 scopus 로고
    • Communicating hydrocephalus from subarachnoid bleeding
    • Foltz E.L., Ward A.A. Communicating hydrocephalus from subarachnoid bleeding. J. Neurosurg. 13:1956;546-548.
    • (1956) J. Neurosurg. , vol.13 , pp. 546-548
    • Foltz, E.L.1    Ward, A.A.2
  • 5
    • 0014635442 scopus 로고
    • Pre and post-operative evaluation of cerebral blood flow in low-pressure hydrocephalus
    • Greitz T.V.B., Grepe A.O.L., Kalmar M.S.F. Pre and post-operative evaluation of cerebral blood flow in low-pressure hydrocephalus. J. Neurosurg. 31:1969;644-651.
    • (1969) J. Neurosurg. , vol.31 , pp. 644-651
    • Greitz, T.V.B.1    Grepe, A.O.L.2    Kalmar, M.S.F.3
  • 6
    • 0013785967 scopus 로고
    • The special clinical problem of symptomatic hydrocephalus with normal cerebrospinal fluid pressure. Observations on cerebrospinal fluid hydrodynamics
    • Hakim S., Adams R.D. The special clinical problem of symptomatic hydrocephalus with normal cerebrospinal fluid pressure. Observations on cerebrospinal fluid hydrodynamics. J. Neurol. Sci. 2:1965;307-327.
    • (1965) J. Neurol. Sci. , vol.2 , pp. 307-327
    • Hakim, S.1    Adams, R.D.2
  • 8
  • 17
    • 0030028429 scopus 로고    scopus 로고
    • Genetic association between intronic polymorphism in Presenilin-1 gene and late onset Alzheimer's disease
    • Wragg M., Hutton M., Talbot C., Alzheimer's Disease Collaborative Group Genetic association between intronic polymorphism in Presenilin-1 gene and late onset Alzheimer's disease. Lancet. 347:1996;509-512.
    • (1996) Lancet , vol.347 , pp. 509-512
    • Wragg, M.1    Hutton, M.2    Talbot, C.3    Alzheimer'S Disease Collaborative Group4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.