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Volumn 68, Issue 11, 2007, Pages 868-870

Novel prion protein gene mutation presenting with subacute PSP-like syndrome

Author keywords

[No Author keywords available]

Indexed keywords

AMYLOID PROTEIN; PRION PROTEIN; PROTEIN 14 3 3;

EID: 34047199059     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/01.wnl.0000256819.61531.98     Document Type: Article
Times cited : (37)

References (10)
  • 1
    • 0347915581 scopus 로고    scopus 로고
    • Transmissible spongiform encephalopathies
    • Collins SJ, Lawson VA, Masters CL. Transmissible spongiform encephalopathies. Lancet 2004;363:51-61.
    • (2004) Lancet , vol.363 , pp. 51-61
    • Collins, S.J.1    Lawson, V.A.2    Masters, C.L.3
  • 2
    • 0032816292 scopus 로고    scopus 로고
    • Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects
    • Parchi P, Giese A, Capellari S, et al. Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects. Ann Neurol 1999;46:224-233.
    • (1999) Ann Neurol , vol.46 , pp. 224-233
    • Parchi, P.1    Giese, A.2    Capellari, S.3
  • 3
    • 0141502270 scopus 로고    scopus 로고
    • Diagnostic accuracy of progressive supranuclear palsy in the Society for Progressive Supranuclear Palsy Brain Bank
    • Josephs KA, Dickson DW. Diagnostic accuracy of progressive supranuclear palsy in the Society for Progressive Supranuclear Palsy Brain Bank. Mov Disord 2003;18:1018-1026.
    • (2003) Mov Disord , vol.18 , pp. 1018-1026
    • Josephs, K.A.1    Dickson, D.W.2
  • 4
    • 0026662717 scopus 로고
    • Familial Creutzfeldt-Jakob disease (codon 200 mutation) with supranuclear palsy
    • Bertoni JM, Brown P, Goldfarb LG, et al. Familial Creutzfeldt-Jakob disease (codon 200 mutation) with supranuclear palsy. JAMA 1992;268:2413-2415.
    • (1992) JAMA , vol.268 , pp. 2413-2415
    • Bertoni, J.M.1    Brown, P.2    Goldfarb, L.G.3
  • 5
    • 0026500302 scopus 로고
    • Abnormal eye movements in Gerstmann-Sträussler-Scheinker disease
    • Yee RD, Farlow MR, Suzuki DA, et al. Abnormal eye movements in Gerstmann-Sträussler-Scheinker disease. Arch Ophthalmol 1992;110:68-74.
    • (1992) Arch Ophthalmol , vol.110 , pp. 68-74
    • Yee, R.D.1    Farlow, M.R.2    Suzuki, D.A.3
  • 6
    • 0038476177 scopus 로고    scopus 로고
    • Novel prion protein insert mutation associated with prolonged neurodegenerative illness
    • Lewis V, Collins S, Hill AF, et al. Novel prion protein insert mutation associated with prolonged neurodegenerative illness. Neurology 2003;60:1620-1624.
    • (2003) Neurology , vol.60 , pp. 1620-1624
    • Lewis, V.1    Collins, S.2    Hill, A.F.3
  • 7
    • 0029063658 scopus 로고
    • New variant prion protein in a Japanese family with Gerstmann-Sträussler syndrome
    • Furukawa H, Kitamoto T, Tanaka Y, Tateishi J. New variant prion protein in a Japanese family with Gerstmann-Sträussler syndrome. Brain Res Mol Brain Res 1995;30:385-388.
    • (1995) Brain Res Mol Brain Res , vol.30 , pp. 385-388
    • Furukawa, H.1    Kitamoto, T.2    Tanaka, Y.3    Tateishi, J.4
  • 8
    • 0033926960 scopus 로고    scopus 로고
    • Creutzfeldt-Jakob disease and the eye. II. Ophthalmic and neuro-ophthalmic features
    • Lueck CJ, McIlwaine GG, Zeidler M. Creutzfeldt-Jakob disease and the eye. II. Ophthalmic and neuro-ophthalmic features. Eye 2000;14:291-301.
    • (2000) Eye , vol.14 , pp. 291-301
    • Lueck, C.J.1    McIlwaine, G.G.2    Zeidler, M.3
  • 9
    • 8944226575 scopus 로고    scopus 로고
    • Clinical research criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome): Report of the NINDS-SPSP International Workshop
    • Litvan I, Agid Y, Calne D, et al. Clinical research criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome): report of the NINDS-SPSP International Workshop. Neurology 1996;47:1-9.
    • (1996) Neurology , vol.47 , pp. 1-9
    • Litvan, I.1    Agid, Y.2    Calne, D.3
  • 10
    • 0025134309 scopus 로고
    • Familial Creutzfeldt-Jakob disease without periodic EEG activity
    • Tietjen GE, Drury I. Familial Creutzfeldt-Jakob disease without periodic EEG activity. Ann Neurol 1990;28:585-588.
    • (1990) Ann Neurol , vol.28 , pp. 585-588
    • Tietjen, G.E.1    Drury, I.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.