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Machado-Joseph disease: A proposal of spastic paraplegic subtype.

作者信息

Sakai T, Kawakami H

机构信息

Department of Neurology, National Chikugo Hospital, Fukuoka, Japan.

出版信息

Neurology. 1996 Mar;46(3):846-7.

PMID:8618704
Abstract
摘要

相似文献

1
Machado-Joseph disease: A proposal of spastic paraplegic subtype.马查多-约瑟夫病:痉挛性截瘫亚型的一种提议。
Neurology. 1996 Mar;46(3):846-7.
2
[The characteristics and the gene locus of Machado Joseph disease].[马查多-约瑟夫病的特征及基因位点]
No To Shinkei. 1995 Feb;47(2):117-29.
3
Unique features of the CAG repeats in Machado-Joseph disease.马查多-约瑟夫病中CAG重复序列的独特特征。
Nat Genet. 1995 Apr;9(4):344-5. doi: 10.1038/ng0495-344.
4
The Lewis family revisited: no evidence for autosomal dominant multiple system atrophy.再探刘易斯家族:无证据支持常染色体显性遗传性多系统萎缩症
Parkinsonism Relat Disord. 2005 Sep;11(6):363-5. doi: 10.1016/j.parkreldis.2005.06.001.
5
Intrafamilial variability in Machado-Joseph disease.
Mov Disord. 1996 Nov;11(6):741-3. doi: 10.1002/mds.870110625.
6
Fatigue and daytime somnolence in Machado Joseph Disease (spinocerebellar ataxia type 3).马查多-约瑟夫病(脊髓小脑共济失调3型)中的疲劳和日间嗜睡
Mov Disord. 2008 Jul 15;23(9):1323-4. doi: 10.1002/mds.22122.
7
A case of Machado-Joseph disease presenting with spastic paraparesis.1例以痉挛性截瘫为表现的马查多-约瑟夫病
J Neurol Neurosurg Psychiatry. 1997 May;62(5):542-3. doi: 10.1136/jnnp.62.5.542-a.
8
Machado-Joseph shoe.马查多-约瑟夫病
Mov Disord. 2005 Jan;20(1):66-8. doi: 10.1002/mds.20277.
9
Non-movement disorder heralds symptoms of Machado-Joseph disease years before ataxia.在共济失调出现数年之前,非运动障碍就预示着马查多-约瑟夫病的症状。
Mov Disord. 2005 Jun;20(6):739-41. doi: 10.1002/mds.20419.
10
Cognitive impairments in Machado-Joseph disease.马查多-约瑟夫病中的认知障碍。
Arch Neurol. 2004 Nov;61(11):1757-60. doi: 10.1001/archneur.61.11.1757.

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Disease Progression and Multiparametric Imaging Characteristics of Spinocerebellar Ataxia Type 3 With Spastic Paraplegia.伴有痉挛性截瘫的3型脊髓小脑共济失调的疾病进展和多参数成像特征
Neurol Genet. 2024 Jun 4;10(3):e200162. doi: 10.1212/NXG.0000000000200162. eCollection 2024 Jun.
2
Spinocerebellar ataxia type 3 in Israel: phenotype and genotype of a Jew Yemenite subpopulation.以色列的3型脊髓小脑共济失调:也门犹太亚群的表型和基因型
J Neurol. 2016 Nov;263(11):2207-2214. doi: 10.1007/s00415-016-8251-8. Epub 2016 Aug 8.
3
Pearls & Oy-sters: Spinocerebellar ataxia type 3 presenting with cervical dystonia without ataxia.
要点与难点:3型脊髓小脑共济失调表现为颈部肌张力障碍而无共济失调。
Neurology. 2016 Jan 5;86(1):e1-3. doi: 10.1212/WNL.0000000000002232.
4
Subjects At-Risk for Genetic Diseases in Portugal: Illness Representations.葡萄牙遗传疾病高危人群:疾病认知
J Genet Couns. 2016 Feb;25(1):79-89. doi: 10.1007/s10897-015-9846-4. Epub 2015 May 19.
5
Spinocerebellar ataxia type 3/Machado-Joseph disease manifested as spastic paraplegia: A clinical and genetic study.表现为痉挛性截瘫的3型脊髓小脑共济失调/马查多-约瑟夫病:一项临床与遗传学研究
Exp Ther Med. 2015 Feb;9(2):417-420. doi: 10.3892/etm.2014.2136. Epub 2014 Dec 16.
6
Striatal dopaminergic functioning in patients with sporadic and hereditary spastic paraplegias with parkinsonism.纹状体多巴胺能功能在散发型和遗传性痉挛性截瘫伴帕金森病患者中的变化。
J Korean Med Sci. 2013 Nov;28(11):1661-6. doi: 10.3346/jkms.2013.28.11.1661. Epub 2013 Oct 31.
7
Toward understanding Machado-Joseph disease.理解马查多-约瑟夫病。
Prog Neurobiol. 2012 May;97(2):239-57. doi: 10.1016/j.pneurobio.2011.11.006. Epub 2011 Nov 23.
8
Machado-Joseph Disease: from first descriptions to new perspectives.马查多-约瑟夫病:从最初的描述到新视角。
Orphanet J Rare Dis. 2011 Jun 2;6:35. doi: 10.1186/1750-1172-6-35.
9
Caring for Machado-Joseph disease: current understanding and how to help patients.照顾 Machado-Joseph 病:当前的认识和如何帮助患者。
Parkinsonism Relat Disord. 2010 Jan;16(1):2-7. doi: 10.1016/j.parkreldis.2009.08.012. Epub 2009 Oct 6.
10
A case of Machado-Joseph disease presenting with spastic paraparesis.1例以痉挛性截瘫为表现的马查多-约瑟夫病
J Neurol Neurosurg Psychiatry. 1997 May;62(5):542-3. doi: 10.1136/jnnp.62.5.542-a.