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Volumn 49, Issue 2, 1997, Pages 593-595

Detection of 14-3-3 protein in the CSF of genetic Creutzfeldt Jakob disease

Author keywords

[No Author keywords available]

Indexed keywords

PROTEIN;

EID: 0030766643     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.49.2.593     Document Type: Article
Times cited : (52)

References (10)
  • 1
    • 0028625478 scopus 로고
    • Neurodegeneration in humans caused by prions
    • Prusiner SB. Neurodegeneration in humans caused by prions. West J Med 1994;161:264-272.
    • (1994) West J Med , vol.161 , pp. 264-272
    • Prusiner, S.B.1
  • 2
    • 0027443351 scopus 로고
    • Clinical heterogeneity and unusual presentations of Creutzfeldt-Jakob disease in Jewish patients with the PRNP codon 200 mutation
    • Chapman J, Brown P, Goldfarb LG, Arlazoroff A, Gajdusek DC, Korczyn AD. Clinical heterogeneity and unusual presentations of Creutzfeldt-Jakob disease in Jewish patients with the PRNP codon 200 mutation. J Neurol Neurosurg Psychiatry 1993;56:1109-1112.
    • (1993) J Neurol Neurosurg Psychiatry , vol.56 , pp. 1109-1112
    • Chapman, J.1    Brown, P.2    Goldfarb, L.G.3    Arlazoroff, A.4    Gajdusek, D.C.5    Korczyn, A.D.6
  • 4
    • 0028032296 scopus 로고
    • 14-3-3: Modulators of the signaling proteins?
    • Morrison D. 14-3-3: modulators of the signaling proteins? Science 1994;266:56-57.
    • (1994) Science , vol.266 , pp. 56-57
    • Morrison, D.1
  • 5
    • 0029840653 scopus 로고    scopus 로고
    • The 14-3-3 brain protein in cerebrospinal fluid as a marker for transmissible spongiform encephalopathies
    • Hsich G, Kenney K, Gibbs CJ, Lee KH, Harrington MG. The 14-3-3 brain protein in cerebrospinal fluid as a marker for transmissible spongiform encephalopathies. New Engl J Med 1996;335:924-930.
    • (1996) New Engl J Med , vol.335 , pp. 924-930
    • Hsich, G.1    Kenney, K.2    Gibbs, C.J.3    Lee, K.H.4    Harrington, M.G.5
  • 6
    • 0022606619 scopus 로고
    • Abnormal proteins in the cerebrospinal fluid of patients with Creutzfeldt-Jakob disease
    • Harrington MG, Merril CR, Asher DM, Gajdusek DC. Abnormal proteins in the cerebrospinal fluid of patients with Creutzfeldt-Jakob disease. N Engl J Med 1986;315:279-283.
    • (1986) N Engl J Med , vol.315 , pp. 279-283
    • Harrington, M.G.1    Merril, C.R.2    Asher, D.M.3    Gajdusek, D.C.4
  • 8
    • 0030604908 scopus 로고    scopus 로고
    • Diagnosis of CJD by two-dimensional gel electrophoresis of CSF
    • Zerr I, Bodemer M, Otto M, et al. Diagnosis of CJD by two-dimensional gel electrophoresis of CSF. Lancet 1996;348:846-849.
    • (1996) Lancet , vol.348 , pp. 846-849
    • Zerr, I.1    Bodemer, M.2    Otto, M.3
  • 9
    • 0025869213 scopus 로고
    • Mutation of the prion protein in Libyan Jews with Creutzfeldt-Jakob disease
    • Hsiao K, Meiner Z, Kahana E, et al. Mutation of the prion protein in Libyan Jews with Creutzfeldt-Jakob disease. N Engl J Med 1991;324:1091-1097.
    • (1991) N Engl J Med , vol.324 , pp. 1091-1097
    • Hsiao, K.1    Meiner, Z.2    Kahana, E.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.