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Volumn 39, Issue 1, 2001, Pages 27-31

Report on the first Polish case of the Gerstmann-Sträussler-Scheinker syndrome

Author keywords

Amyloid deposits; Cerebellar cortex; Creutzfeldt Jakob disease; Gene mutation; Gerstmann Str ussler Scheinker syndrome; Prion protein

Indexed keywords

METHIONINE; MONOCLONAL ANTIBODY; MONOCLONAL ANTIBODY 3F4; PRION PROTEIN; UNCLASSIFIED DRUG;

EID: 0035784145     PISSN: 00283894     EISSN: 1509572X     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (13)

References (9)
  • 1
    • 9544219691 scopus 로고    scopus 로고
    • Polymorphism at codon 129 or codon 219 of PRNP and clinical heterogeneity in a previously unreported family with Gerstmann-Sträussler-Scheinker disease (PrP-P102 mutation)
    • Barbanti P, Fabrini G, Salvatore M, Petraroli R, Cardone F, Maras B, Equestre M, Macchi G, Lenzi GL, Pocchiani M. (1996) Polymorphism at codon 129 or codon 219 of PRNP and clinical heterogeneity in a previously unreported family with Gerstmann-Sträussler-Scheinker disease (PrP-P102 mutation). Neurology, 47, 3: 734-741.
    • (1996) Neurology , vol.47 , Issue.3 , pp. 734-741
    • Barbanti, P.1    Fabrini, G.2    Salvatore, M.3    Petraroli, R.4    Cardone, F.5    Maras, B.6    Equestre, M.7    Macchi, G.8    Lenzi, G.L.9    Pocchiani, M.10
  • 2
    • 0025859996 scopus 로고
    • Genetic predisposition to iatrogenic Creutzfeld-Jakob disease
    • Collinge J, Palmer MS, Dryden AJ (1991). Genetic predisposition to iatrogenic Creutzfeld-Jakob disease. Lancet, 337: 1141-1142.
    • (1991) Lancet , vol.337 , pp. 1141-1442
    • Collinge, J.1    Palmer, M.S.2    Dryden, A.J.3
  • 3
    • 0000540668 scopus 로고
    • Uber eigenartige herediatart-familiare Erkrankung des Zentralner-vensystems
    • Gerstmann J, Sträussler E, Shcheinker I. (1936). Uber eigenartige herediatart-familiare Erkrankung des Zentralner-vensystems. Z Neurol, 154: 736-762.
    • (1936) Z Neurol , vol.154 , pp. 736-762
    • Gerstmann, J.1    Sträussler, E.2    Shcheinker, I.3
  • 8
    • 0030873721 scopus 로고    scopus 로고
    • Neurofibrillary tangles in Gerstmann-Sträussler-Scheinker syndrome with the A117 prion gene mutation
    • Tranchant C, Sergeant N, Wattez A, Mohr M, Warter JM, Delacourte A (1997) Neurofibrillary tangles in Gerstmann-Sträussler-Scheinker syndrome with the A117 prion gene mutation. J Neurol Neurosurg Psych, 63, 2: 240-246.
    • (1997) J Neurol Neurosurg Psych , vol.63 , Issue.2 , pp. 240-246
    • Tranchant, C.1    Sergeant, N.2    Wattez, A.3    Mohr, M.4    Warter, J.M.5    Delacourte, A.6
  • 9
    • 0031026861 scopus 로고    scopus 로고
    • Gerstmann-Sträussler-Scheinker disease with the PRNP P102L mutation and valine at codon 129
    • Young K, Clark HB, Piccardo P, Dlouhy SR, Ghetti B (1997) Gerstmann-Sträussler-Scheinker disease with the PRNP P102L mutation and valine at codon 129. Mol Brain Res, 44, 1: 147-150.
    • (1997) Mol Brain Res , vol.44 , Issue.1 , pp. 147-150
    • Young, K.1    Clark, H.B.2    Piccardo, P.3    Dlouhy, S.R.4    Ghetti, B.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.