期刊文献+
任意字段
题名或关键词
题名
关键词
文摘
作者
第一作者
机构
刊名
分类号
参考文献
作者简介
基金资助
栏目信息

额颞叶痴呆的研究进展 被引量：3

下载PDF
导出
摘要 额颞叶痴呆是一种原发性退行性痴呆,核心症状为缓慢发生、进行性加重的行为和语言障碍。本文就其分子生物学、神经病理、临床诊断、影像学及神经心理学等方面的研究进展进行综述。
作者 马爱军 张本恕
机构地区 天津医科大学总医院神经内科
出处 《国际神经病学神经外科学杂志》 2006年第3期285-288,共4页 Journal of International Neurology and Neurosurgery
关键词 额颞叶 痴呆 PICK病 TAU
分类号 R749.1 [医药卫生—神经病学与精神病学]
  • 相关文献

参考文献25

  • 1Goldman JS,Farmer JM,Van Deerlin VM,et al.Frontotemporal dementia:genetics and genetic counseling dilemmas.Neurologist,2004,10(5):227-234.
  • 2Ratnavalli E,Brayne C,Dawson K,et al.The prevalence of frontotemporal dementia.Neurology,2002,58 (11):1615-1621.
  • 3Odawara T,Shiozaki K,Iseki E,et al.Alterations of muscarinic acetylcholine receptors in atypical Pick's disease without Pick bodies.J Neurol Neurosurg Psychiatry,2003,74 (7):965 -967.
  • 4Rosso SM,Donker KL,Baks T,et al.Frontotemporal dementia in the Netherlands:patient characteristics and prevalence estimates from a population-based study.Brain,2003,126(9):2016-2022.
  • 5Morris HR,Khan MN,Janssen JC,et al.The genetic and pathological classification of familial frontotemporal dementia.Arch Neurol,2001,58(11):1813-1816.
  • 6Neill GR,Bryan W.Frontotemporal dementia.CONTINUUM:Lifelong Learning in Neurology,2004,10(1):58-80.
  • 7Barghorn S,Zheng-Fischhofer Q,Ackmann M,et al.Structure,microtubule interactions,and paired helical filament aggregation by tau mutants of frontotemporal dementias.Biochemistry,2000,39(38):11714-11721.
  • 8Grover A,England E,Baker M,et al.A novel tau mutation in exon 9 (1260V) causes a four-repeat tauopathy.Exp Neurol,2003,184(1):131-140.
  • 9Hosler BA,Siddique T,Sapp PC,et al.Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22.JAMA,2000,284(13):1664-1669.
  • 10Wilhelmsen KC,Forman MS,Rosen H J,et al.17q-linked frontotemporal dementia -amyotrophic lateral sclerosis without tau mutations with tau and alpha-synuclein inclusions.Arch Neurol,2004,61(3):398-406.

同被引文献109

  • 1Ikeda M, lshikawa T, Tanabe H. Epidemiology of frontotemporal lobar degeneration. Dement Geriatr Cogn Disord, 2004, 17(4) : 265-268.
  • 2Rohrer JD, Guerreiro R, Vandrovcova J, et al. The heritability and genetics of frontotemporal lobar degeneration. Neurology, 2009, 73(18): 1451-1456.
  • 3Wilhelmsen KC, Lynch T, Pavlou E, et al. Localization of disinhibition-dementia-parkinsonism-amyotrophy complex to 17q21-22. Am J Hum Genet, 1994, 55(6): 1159- 1165.
  • 4Foster NL, Wilhelmsen K, Sima AA, et ah Frontotemporal dementia and parkinsonism linked to chromosome 17: a consensus conference. Conference Participants. Ann Neurol, 1997, 41(6) : 706-715.
  • 5Hutton M, Lendon CL, Rizzu P, et al. Association of missense and 5 ' -splice-site mutations in tau with the inherited dementia FTDP-17. Nature, 1998 , 393 ( 6686 ) : 702- 705.
  • 6Poorkaj P, Bird TD, Wijsman E, et al. Tau is a candidate gene for chromosome 17 frontotemporal dementia. Ann Neurol, 1998, 43(6) : 815-825.
  • 7Andreadis A, Brown WM, Kosik KS. Structure and novel exons of the human tau gene. Biochemistry, 1992, 31 ( 4-3 ) : 10626-10633.
  • 8Kaivorinne AL, Kruger J, Kuivaniemi K, et al. Role of MAPT mutations and haplotype in frontotemporal lobar degeneration in Northern Finland. BMC Neurol, 2008, 8: 48.
  • 9Picketing-Brown SM, Rollinson S, Du Plessis D, et al. Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known mutations. Brain, 2008, 131 (Pt 3) : 721-731.
  • 10Rizzu P, Van Swieten JC, Joosse M, et al. High prevalence of mutations in the microtubule-associated protein tan in a population study of frontotemporal dementia in the Netherlands. Am J Hum Genet, 1999, 64(2) : 414-421.

引证文献3

二级引证文献11

国际神经病学神经外科学杂志
2006年 第3期

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部