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Generalized myoclonus as a prominent symptom in a patient with FTLD-TDP.

作者信息

Pail Martin, Matej Radoslav, Husarova Ivica, Rektorova Irena

出版信息

J Neurol. 2013 Jun;260(6):1681-3. doi: 10.1007/s00415-013-6942-y. Epub 2013 May 9.

DOI:10.1007/s00415-013-6942-y
PMID:23657632
Abstract
摘要

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本文引用的文献

1
EFNS-ENS Guidelines on the diagnosis and management of disorders associated with dementia.EFNS-ENS 指南:痴呆相关疾病的诊断与管理。
Eur J Neurol. 2012 Sep;19(9):1159-79. doi: 10.1111/j.1468-1331.2012.03784.x.
2
Clinical and neuroanatomical signatures of tissue pathology in frontotemporal lobar degeneration.额颞叶变性的组织病理学的临床和神经解剖学特征。
Brain. 2011 Sep;134(Pt 9):2565-81. doi: 10.1093/brain/awr198.
3
Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia.修订后的额颞叶痴呆行为变异型诊断标准的敏感性。
Brain. 2011 Sep;134(Pt 9):2456-77. doi: 10.1093/brain/awr179. Epub 2011 Aug 2.
4
A harmonized classification system for FTLD-TDP pathology.额颞叶痴呆-嗜银颗粒蛋白病(FTLD-TDP)病理学的统一分类系统。
Acta Neuropathol. 2011 Jul;122(1):111-3. doi: 10.1007/s00401-011-0845-8. Epub 2011 Jun 5.
5
Isolated continuous lingual myoclonus: unusual presentation of amyotrophic lateral sclerosis.
Mov Disord. 2010 Jul 15;25(9):1309-10. doi: 10.1002/mds.23099.
6
Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease.散发性 Creutzfeldt-Jakob 病的临床诊断标准更新版。
Brain. 2009 Oct;132(Pt 10):2659-68. doi: 10.1093/brain/awp191. Epub 2009 Sep 22.
7
Novel splicing mutation in the progranulin gene causing familial corticobasal syndrome.原纤维蛋白基因中的新型剪接突变导致家族性皮质基底节综合征。
Brain. 2006 Nov;129(Pt 11):3115-23. doi: 10.1093/brain/awl276. Epub 2006 Oct 9.
8
Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis.额颞叶痴呆和肌萎缩侧索硬化症中泛素化的TDP-43
Science. 2006 Oct 6;314(5796):130-3. doi: 10.1126/science.1134108.
9
Myoclonus and neurodegenerative disease--what's in a name?肌阵挛与神经退行性疾病——名称中有何含义?
Parkinsonism Relat Disord. 2003 Mar;9(4):185-92. doi: 10.1016/s1353-8020(02)00054-8.
10
Definition and classification of myoclonus.
Adv Neurol. 1986;43:1-5.