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Volumn 47, Issue 5, 1996, Pages 1326-1328

Fatal familial insomnia: A seventh family

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; BASAL GANGLION; BRAIN ATROPHY; CASE REPORT; CLINICAL PROTOCOL; COMPUTER ASSISTED TOMOGRAPHY; DEMENTIA; DNA DETERMINATION; FAMILY; FEMALE; GENE MUTATION; GLIOSIS; HUMAN; HUMAN TISSUE; MALE; NERVE CELL LESION; PRION DISEASE; PRIORITY JOURNAL;

EID: 0029854307     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.47.5.1326     Document Type: Article
Times cited : (19)

References (10)
  • 1
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  • 2
    • 0026552043 scopus 로고
    • Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene
    • Medori R, Tritschler HJ, LeBlanc A, et al. Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene. N Engl J Med 1992;326:444-449.
    • (1992) N Engl J Med , vol.326 , pp. 444-449
    • Medori, R.1    Tritschler, H.J.2    LeBlanc, A.3
  • 3
    • 0026496257 scopus 로고
    • Fatal familial insomnia and familial Creutzfeldt-Jakob disease: Disease phenotype determined by a DNA polymorphism
    • Goldfarb LG, Petersen RB, Tabaton M, et al. Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism. Science 1992; 258:806-808.
    • (1992) Science , vol.258 , pp. 806-808
    • Goldfarb, L.G.1    Petersen, R.B.2    Tabaton, M.3
  • 4
    • 0026690906 scopus 로고
    • Fatal familial insomnia: A second kindred with mutation of prion gene at codon 178
    • Medori R, Montagna P, Tritschler HJ, et al. Fatal familial insomnia: a second kindred with mutation of prion gene at codon 178. Neurology 1992;42:669-670.
    • (1992) Neurology , vol.42 , pp. 669-670
    • Medori, R.1    Montagna, P.2    Tritschler, H.J.3
  • 5
    • 0026785544 scopus 로고
    • Analysis of the prion gene in thalamic dementia
    • Petersen RB, Tabaton M, Berg L, et al. Analysis of the prion gene in thalamic dementia. Neurology 1992;42:1859-1863.
    • (1992) Neurology , vol.42 , pp. 1859-1863
    • Petersen, R.B.1    Tabaton, M.2    Berg, L.3
  • 6
    • 0027763639 scopus 로고
    • Fatal familial insomnia and the widening spectrum of prion diseases
    • Gambetti P, Petersen R, Monari L, et al. Fatal familial insomnia and the widening spectrum of prion diseases. Br Med Bull 1993;49:980-994.
    • (1993) Br Med Bull , vol.49 , pp. 980-994
    • Gambetti, P.1    Petersen, R.2    Monari, L.3
  • 7
    • 0026801958 scopus 로고
    • A PrP gene codon 178 base substitution and a 24-bp interstitial deletion in familial Creutzfeldt-Jakob disease
    • Bosque PJ, Vnencak-Jones C, Johnson MD, Whitlock JA, McLean MJ. A PrP gene codon 178 base substitution and a 24-bp interstitial deletion in familial Creutzfeldt-Jakob disease. Neurology 1992;42:1864-1870.
    • (1992) Neurology , vol.42 , pp. 1864-1870
    • Bosque, P.J.1    Vnencak-Jones, C.2    Johnson, M.D.3    Whitlock, J.A.4    McLean, M.J.5
  • 8
    • 0029031422 scopus 로고
    • Clinical and genetic studies of fatal familial insomnia
    • Reder AT, Mednick AS, Brown P, et al. Clinical and genetic studies of fatal familial insomnia. Neurology 1995;45:1068-1075.
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  • 9
    • 0029961971 scopus 로고    scopus 로고
    • Fatal familial insomnia with a mutation at codon 178 of the prion protein gene
    • Nagayama M, Shinohara Y, Furukawa H, Kitamoto T. Fatal familial insomnia with a mutation at codon 178 of the prion protein gene. Neurology 1996;47:1313-1316.
    • (1996) Neurology , vol.47 , pp. 1313-1316
    • Nagayama, M.1    Shinohara, Y.2    Furukawa, H.3    Kitamoto, T.4
  • 10
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.