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Volumn 73, Issue 2, 2009, Pages 86-87

Familial neurodegeneration in progressive supranuclear palsy: More frequent than expected?

Author keywords

[No Author keywords available]

Indexed keywords

TAU PROTEIN; MAPT PROTEIN, HUMAN;

EID: 68149108184     PISSN: 00283878     EISSN: 1526632X     Source Type: Journal    
DOI: 10.1212/WNL.0b013e3181aa2a71     Document Type: Editorial
Times cited : (4)

References (11)
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    • Steele JC, Richardson JC, Olszewski J. Progressive supranuclear palsy: a heterogeneous degeneration involving the brainstem, basal ganglia and cerebellum with vertical gaze and pseudobulbar palsy: nuchal dystonia and dementia. Arch Neurol 1964;10:333-359.
    • (1964) Arch Neurol , vol.10 , pp. 333-359
    • Steele, J.C.1    Richardson, J.C.2    Olszewski, J.3
  • 2
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    • Familial aggregation of parkinsonism in progressive supranuclear palsy
    • Donker Kaat L, Boon AJW, Azmani A, et al. Familial aggregation of parkinsonism in progressive supranuclear palsy. Neurology 2009;73:98-105.
    • (2009) Neurology , vol.73 , pp. 98-105
    • Donker Kaat, L.1    Boon, A.J.W.2    Azmani, A.3
  • 3
    • 20444436764 scopus 로고    scopus 로고
    • Characteristics of two distinct clinical phenotypes in pathologically proven progressive supranuclear palsy: Richardson's syndrome and PSP-parkinsonism
    • Williams DR, de Silva R, Paviour DC, et al. Characteristics of two distinct clinical phenotypes in pathologically proven progressive supranuclear palsy: Richardson's syndrome and PSP-parkinsonism. Brain 2005;128:1247-1258.
    • (2005) Brain , vol.128 , pp. 1247-1258
    • Williams, D.R.1    de Silva, R.2    Paviour, D.C.3
  • 6
    • 0035134195 scopus 로고    scopus 로고
    • Familial atypical progressive supranuclear palsy associated with homozygosity for the delN296 mutation in the tau gene
    • Pastor P, Pastor E, Carnero C, et al. Familial atypical progressive supranuclear palsy associated with homozygosity for the delN296 mutation in the tau gene. Ann Neurol 2001;49:263-267.
    • (2001) Ann Neurol , vol.49 , pp. 263-267
    • Pastor, P.1    Pastor, E.2    Carnero, C.3
  • 7
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    • Tau phosphorylation and kinase activation in familial tauopathy linked to deln296 mutation
    • Ferrer I, Pastor P, Rey MJ, et al. Tau phosphorylation and kinase activation in familial tauopathy linked to deln296 mutation. Neuropathol Appl Neurobiol 2003;29:23-34.
    • (2003) Neuropathol Appl Neurobiol , vol.29 , pp. 23-34
    • Ferrer, I.1    Pastor, P.2    Rey, M.J.3
  • 8
    • 0031044850 scopus 로고    scopus 로고
    • Genetic evidence for the involvement of tau in progressive supranuclear palsy
    • Conrad C, Andreadis A, Trojanowski JQ, et al. Genetic evidence for the involvement of tau in progressive supranuclear palsy. Ann Neurol 1997;41:277-281.
    • (1997) Ann Neurol , vol.41 , pp. 277-281
    • Conrad, C.1    Andreadis, A.2    Trojanowski, J.Q.3
  • 9
    • 27744488802 scopus 로고    scopus 로고
    • High-density SNP haplotyping suggests altered regulation of tau gene expression in progressive supranuclear palsy
    • Rademakers R, Melquist S, Cruts M, et al. High-density SNP haplotyping suggests altered regulation of tau gene expression in progressive supranuclear palsy. Hum Mol Genet 2005;14:3281-3292.
    • (2005) Hum Mol Genet , vol.14 , pp. 3281-3292
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  • 10
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    • 5′-Upstream variants of CRHR1 and MAPT genes associated with age at onset in progressive supranuclear palsy and cortical basal degeneration
    • Cruchaga C, Vidal-Taboada JM, Ezquerra M, et al. 5′-Upstream variants of CRHR1 and MAPT genes associated with age at onset in progressive supranuclear palsy and cortical basal degeneration. Neurobiol Dis 2009;33:164-170.
    • (2009) Neurobiol Dis , vol.33 , pp. 164-170
    • Cruchaga, C.1    Vidal-Taboada, J.M.2    Ezquerra, M.3
  • 11
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    • Genetic linkage of autosomal dominant progressive supranuclear palsy to 1q31.1
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.