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Volumn 34, Issue 3, 2008, Pages 366-370

Frontotemporal dementia and Parkinsonism linked to chromosome 17 in a young Australian patient with the G389R Tau mutation

Author keywords

[No Author keywords available]

Indexed keywords

TAU PROTEIN;

EID: 42549148803     PISSN: 03051846     EISSN: 13652990     Source Type: Journal    
DOI: 10.1111/j.1365-2990.2007.00918.x     Document Type: Article
Times cited : (16)

References (22)
  • 6
    • 16244408643 scopus 로고    scopus 로고
    • Slow wave and rem sleep mechanisms are differently altered in hereditary pick disease associated with the TAU G389R mutation
    • Gemignani A, Pietrini P, Murrell JR, Glazier BS, Zolo P, Guazelli M, Ghetti B. Slow wave and rem sleep mechanisms are differently altered in hereditary pick disease associated with the TAU G389R mutation. Arch Ital Biol 2005 143 : 65 79
    • (2005) Arch Ital Biol , vol.143 , pp. 65-79
    • Gemignani, A.1    Pietrini, P.2    Murrell, J.R.3    Glazier, B.S.4    Zolo, P.5    Guazelli, M.6    Ghetti, B.7
  • 8
    • 0028223015 scopus 로고
    • Clinical and neuropathological criteria for frontotemporal dementia
    • The Lund and Manchester groups.
    • The Lund and Manchester groups. Clinical and neuropathological criteria for frontotemporal dementia. J Neurol Neurosurg Psychiatry 1994 57 : 416 18
    • (1994) J Neurol Neurosurg Psychiatry , vol.57 , pp. 416-18
  • 11
    • 0028073692 scopus 로고
    • Localization of disinhibition-dementia-parkinsonism-amyotrophy complex to 17q21-22
    • Wilhelmsen KC, Lynch T, Pavlou E, Higgins M, Nygaard TG. Localization of disinhibition-dementia-parkinsonism-amyotrophy complex to 17q21-22. Am J Hum Genet 1994 55 : 1159 65
    • (1994) Am J Hum Genet , vol.55 , pp. 1159-65
    • Wilhelmsen, K.C.1    Lynch, T.2    Pavlou, E.3    Higgins, M.4    Nygaard, T.G.5
  • 21
    • 0034534951 scopus 로고    scopus 로고
    • Progress in hereditary tauopathies: A mutation in the Tau gene (G389R) causes a pick disease - Like syndrome
    • Ghetti B, Murrell JR, Zolo P, Spillantini MG, Goedert M. Progress in hereditary tauopathies: a mutation in the Tau gene (G389R) causes a pick disease - like syndrome. Ann N Y Acad Sci 2000 920 : 52 62
    • (2000) Ann N Y Acad Sci , vol.920 , pp. 52-62
    • Ghetti, B.1    Murrell, J.R.2    Zolo, P.3    Spillantini, M.G.4    Goedert, M.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.