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再探非阿尔茨海默型额叶变性

Frontal lobe degeneration of non-Alzheimer type revisited.

作者信息

Brun A

机构信息

Neuropathology Division, University Hospital, Lund, Sweden.

出版信息

Dementia. 1993 May-Aug;4(3-4):126-31. doi: 10.1159/000107311.

DOI:10.1159/000107311
PMID:8401779
Abstract

The neuropathology of frontal lobe degeneration of non-Alzheimer type was reevaluated on the basis of a new material of 13 cases against the background of experiences from earlier published 16 cases. The salient neuropathological feature was an unspecific neuronal degeneration of superficial cortical layers of the frontal and to some extent the temporal lobes without markers for Alzheimer's, Pick's or Lewy body diseases and there were no indications so far of a prion etiology. The consistency of histopathological features are taken to indicate a disease entity, also identified by other authors. It is tentatively grouped together with progressive and aphasic dementia, similar cases in the literature and possibly also Pick's disease and ALS with dementia.

摘要

基于13例新病例材料,并结合之前发表的16例病例的经验,对非阿尔茨海默型额叶变性的神经病理学进行了重新评估。显著的神经病理学特征是额叶及部分颞叶浅层皮质层出现非特异性神经元变性,无阿尔茨海默病、皮克病或路易体病的标志物,目前也没有朊病毒病因的迹象。组织病理学特征的一致性表明这是一种疾病实体,其他作者也有相同发现。它暂被归为进行性失语性痴呆、文献中类似病例,可能还包括皮克病以及伴有痴呆的肌萎缩侧索硬化症。

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1
Frontal lobe degeneration of non-Alzheimer type revisited.再探非阿尔茨海默型额叶变性
Dementia. 1993 May-Aug;4(3-4):126-31. doi: 10.1159/000107311.
2
Frontal lobe degeneration of non-Alzheimer type. I. Neuropathology.非阿尔茨海默型额叶变性。I.神经病理学
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[Where fronto-temporal dementia should be placed in the history of Pick's disease and related disorders].额颞叶痴呆在匹克氏病及相关疾病史中的定位
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Hippocampal and neocortical ubiquitin-immunoreactive inclusions in amyotrophic lateral sclerosis with dementia.
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Quantitative neuropathologic analysis of Pick's disease cases: cortical distribution of Pick bodies and coexistence with Alzheimer's disease.匹克氏病病例的定量神经病理学分析:匹克小体的皮质分布及与阿尔茨海默病的共存情况
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Frontal lobe degeneration of non-Alzheimer type.非阿尔茨海默型额叶变性
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选择性靶向额颞叶痴呆的神经元揭示了早期 TDP-43 病理生物学。
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Frontotemporal Dementia.额颞叶痴呆
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Chronic traumatic encephalopathy and other neurodegenerative proteinopathies.慢性创伤性脑病和其他神经退行性蛋白病。
Front Hum Neurosci. 2014 Jan 31;8:30. doi: 10.3389/fnhum.2014.00030. eCollection 2014.
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Familial Lund frontotemporal dementia caused by C9ORF72 hexanucleotide expansion.家族性 Lund 额颞叶痴呆由 C9ORF72 六核苷酸扩展引起。
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Oxidative damage to the promoter region of SQSTM1/p62 is common to neurodegenerative disease.SQSTM1/p62启动子区域的氧化损伤在神经退行性疾病中很常见。
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