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Volumn 8, Issue 3, 1998, Pages 571-575

Conclusions of the Symposium

Author keywords

[No Author keywords available]

Indexed keywords

PRION PROTEIN;

EID: 0031804371     PISSN: 10156305     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1750-3639.1998.tb00185.x     Document Type: Conference Paper
Times cited : (17)

References (28)
  • 1
    • 0026801958 scopus 로고
    • A PrP gene codon 178 base substitution and a 24-bp interstitial deletion in familial CreutzfeldtJakob disease
    • Bosque PJ, Vnencak-Jones CL, Johnson MD, Whitlock JA, McLean MJ. A PrP gene codon 178 base substitution and a 24-bp interstitial deletion in familial CreutzfeldtJakob disease. Neurology 42: 1864-1870, 1992.
    • (1992) Neurology , vol.42 , pp. 1864-1870
    • Bosque, P.J.1    Vnencak-Jones, C.L.2    Johnson, M.D.3    Whitlock, J.A.4    McLean, M.J.5
  • 2
    • 7144245157 scopus 로고    scopus 로고
    • Fatal familial insomnia in the United States, Australia, and Japan
    • this issue
    • Brown P, Cervenakofa L, Powers JM Fatal familial insomnia in the United States, Australia, and Japan. Brain Pathology, this issue.
    • Brain Pathology
    • Brown, P.1    Cervenakofa, L.2    Powers, J.M.3
  • 4
    • 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 56: 1109-1112,1993.
    • (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
  • 6
    • 0013518121 scopus 로고
    • Le syndrome de Creutzfeldt-Jakob et les syndromes corticotnes du presenium (a l'occasion de observations anatomo-cliniques)
    • Garcin R, Brion S, Khochneviss AA. Le syndrome de Creutzfeldt-Jakob et les syndromes corticotnes du presenium (a l'occasion de observations anatomo-cliniques). Rev Neurol (Paris) 109: 419-441, 1963.
    • (1963) Rev Neurol (Paris) , vol.109 , pp. 419-441
    • Garcin, R.1    Brion, S.2    Khochneviss, A.A.3
  • 13
    • 0027490557 scopus 로고
    • Molecular Genetics in Neurology
    • Martin J. Molecular Genetics in Neurology. Ann Neurol 34:757-773, 1993.
    • (1993) Ann Neurol , vol.34 , pp. 757-773
    • Martin, J.1
  • 14
    • 0000181235 scopus 로고
    • Thalamic degeneration
    • Vinken PJ, Bruyn GW (eds). Amsterdam, North-Holland Publishing Company
    • Martin JJ. Thalamic degeneration. Vinken PJ, Bruyn GW (eds). In: Handbook of Clinical Neurology. Volume 21. Amsterdam, North-Holland Publishing Company, pp. 587-604, 1975.
    • (1975) Handbook of Clinical Neurology , vol.21 , pp. 587-604
    • Martin, J.J.1
  • 15
    • 0021073664 scopus 로고
    • Selective thalamic degeneration - Report of a case with memory and mental disturbances
    • Martin JJ, Yap M, Nei IP, Tan TE. Selective thalamic degeneration - Report of a case with memory and mental disturbances. Clin Neuropathol 2: 156-162, 1983.
    • (1983) Clin Neuropathol , vol.2 , pp. 156-162
    • Martin, J.J.1    Yap, M.2    Nei, I.P.3    Tan, T.E.4
  • 16
    • 0030821246 scopus 로고    scopus 로고
    • The D178N (cis-l29M) "fatal familial insomnia" mutation associated with diverse clinicopathologic phenotypes in an Australian kindred
    • McLean CA, Storey E, Gardner RJM, Tannenberg AEG, Cervenakova L, Brown P. The D178N (cis-l29M) "fatal familial insomnia" mutation associated with diverse clinicopathologic phenotypes in an Australian kindred. Neurology 49: 552-558, 1997.
    • (1997) Neurology , vol.49 , pp. 552-558
    • McLean, C.A.1    Storey, E.2    Gardner, R.J.M.3    Tannenberg, A.E.G.4    Cervenakova, L.5    Brown, P.6
  • 19
    • 0029961971 scopus 로고    scopus 로고
    • Fatal familial insomnia with a mutation at codon 178 of the prion protein gene: First report from Japan
    • Nagayama M, Shmohara Y, Furukawa H, Kitamoto T. Fatal familial insomnia with a mutation at codon 178 of the prion protein gene: First report from Japan. Neurology 1996;47:1313-1316.
    • (1996) Neurology , vol.47 , pp. 1313-1316
    • Nagayama, M.1    Shmohara, Y.2    Furukawa, H.3    Kitamoto, T.4
  • 25
    • 0039155548 scopus 로고
    • Bilateral symmetrical degeneration of the thalamus. A clinico-pathological study
    • Schulman S. Bilateral symmetrical degeneration of the thalamus. A clinico-pathological study. J Neuropathol Exp Neurol 16: 446-470, 1957.
    • (1957) J Neuropathol Exp Neurol , vol.16 , pp. 446-470
    • Schulman, S.1
  • 27
    • 0000609757 scopus 로고
    • Severe dementia associated with bilateral symmetricai degeneration of the thalamus
    • Stern K. Severe dementia associated with bilateral symmetricai degeneration of the thalamus. Brain 62:157-171, 1939.
    • (1939) Brain , vol.62 , pp. 157-171
    • Stern, K.1


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