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Volumn 60, Issue 4, 2001, Pages 328-341

Frontal lobe dementia with novel tauopathy: Sporadic multiple system tauopathy with dementia

Author keywords

Corticobasal ganglionic degeneration; Dementia; Frontal lobe dementia; Frontotemporal degeneration; FTDP 17; Progressive supranuclear palsy; Tauopathy

Indexed keywords

SARKOSYL INSOLUBLE TAU PROTEIN; TAU PROTEIN; UNCLASSIFIED DRUG;

EID: 0035063346     PISSN: 00223069     EISSN: None     Source Type: Journal    
DOI: 10.1093/jnen/60.4.328     Document Type: Article
Times cited : (78)

References (73)
  • 7
    • 0039575094 scopus 로고    scopus 로고
    • Comparative biochemistry of tau in progressive supranuclear palsy, corticobasal degeneration, FTDP-17 and Pick's disease
    • (1999) Brain Pathol , vol.9 , pp. 681-693
    • Buée, L.1    Delacourte, A.2
  • 8
    • 0032886469 scopus 로고    scopus 로고
    • Tau-positive glial inclusions in progressive supranuclear palsy, corticobasal degeneration and Pick's disease
    • (1999) Brain Pathol , vol.9 , pp. 663-679
    • Komori, T.1
  • 12
    • 0033009603 scopus 로고    scopus 로고
    • Neurofibrillary degeneration in progressive supranuclear palsy and corticobasal degeneration: Tau pathologies with exclusively "exon 10" isoforms
    • (1999) J Neurochem , vol.72 , pp. 1243-1249
    • Sergeant, N.1    Wattez, A.2    Delacourte, A.3
  • 15
    • 0032833626 scopus 로고    scopus 로고
    • Neuropathologic differentiation of progressive supra-nuclear palsy and corticobasal degeneration
    • (1999) J Neurol , vol.246
    • Dickson, D.W.1
  • 29
    • 0027948959 scopus 로고
    • Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complex
    • (1994) Neurology , vol.44 , pp. 1878-1884
    • Lynch, T.1    Sano, M.2    Marder, K.S.3
  • 33
    • 0032897924 scopus 로고    scopus 로고
    • A clinical pathological comparison of three families with frontotemporal dementia and identical mutations in the tau gene (P301L)
    • (1999) Brain , vol.122 , pp. 741-756
    • Bird, T.D.1    Nochlin, D.2    Poorkaj, P.3
  • 34
    • 0032976201 scopus 로고    scopus 로고
    • From genotype to phenotype: A clinical, pathological, and biochemical investigation of frontotemporal dementia and parkinsonism (FTDP-17) caused by the P301L tau mutation
    • (1999) Ann Neurol , vol.45 , pp. 704-715
    • Nasreddine, Z.S.1    Loginov, M.2    Clark, L.N.3
  • 46
    • 0031045491 scopus 로고    scopus 로고
    • Hereditary frontotemporal dementia is linked to chromosome 17q21-22: A genetic and clinicopathological study of three Dutch families
    • (1997) Ann Neurol , vol.41 , pp. 150-159
    • Heutink, P.1    Stevens, M.2    Rizzu, P.3
  • 51
  • 58
    • 0025908356 scopus 로고
    • The Consortium to Establish a Registry for Alzheimer's Disease (CERAD). Part II. Standardization of the neuropathologic assessment of Alzheimer's disease
    • (1991) Neurology , vol.41 , pp. 479-486
    • Mirra, S.S.1    Heyman, A.2    McKeel, D.3
  • 61
    • 0033545946 scopus 로고    scopus 로고
    • Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17 type, by affecting multiple alternative RNA splicing regulatory elements
    • (1999) Proc Nat Acad Sci USA , vol.96 , pp. 5598-5603
    • D'Souza, I.1    Poorkaj, P.2    Hong, M.3
  • 62
    • 0033591225 scopus 로고    scopus 로고
    • 5′ Splice site mutations in tau associated with the inherited dementia FTDP-17 affect a stem-loop structure that regulates alternative splicing of exon 10
    • (1999) J Biol Chem , vol.274 , pp. 15134-15143
    • Grover, A.1    Houlden, H.2    Baker, M.3
  • 71
    • 0033982344 scopus 로고    scopus 로고
    • Missense tau mutations identified in FTDP-17 have a small effect on tau-microtubule interactions
    • (2000) Brain Res , vol.853 , pp. 5-14
    • DeTure, M.1    Ko, L.2    Yen, S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.