• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Neurofibrillary axonal swellings and amyotrophic lateral sclerosis.

作者信息

Delisle M B, Carpenter S

出版信息

J Neurol Sci. 1984 Feb;63(2):241-50. doi: 10.1016/0022-510x(84)90199-0.

DOI:10.1016/0022-510x(84)90199-0
PMID:6538591
Abstract

A series of 22 cases of amyotrophic lateral sclerosis (ALS) and 22 controls have been assessed for the presence of neurofilamentous accumulations in axons and perikarya. Large axonal swellings were seen in the spinal cord of 12 controls and of 13 ALS cases. When they were present in ALS cases they tended to be much more numerous than in controls, and when they were not present in ALS cases there tended to be severe neuronal loss in the cord. Axonal swelling on lower motor neurons appears to be a significant feature of the pathology of ALS. Its implications in terms of etiology are unknown.

摘要

相似文献

1
Neurofibrillary axonal swellings and amyotrophic lateral sclerosis.
J Neurol Sci. 1984 Feb;63(2):241-50. doi: 10.1016/0022-510x(84)90199-0.
2
Experimental neurotoxic disorders of motor neurons: neurofibrillary pathology.运动神经元的实验性神经毒性疾病:神经原纤维病理学
Adv Neurol. 1982;36:419-33.
3
Axonal swellings in the corticospinal tracts in amyotrophic lateral sclerosis.肌萎缩侧索硬化症中皮质脊髓束的轴突肿胀
Acta Neuropathol. 1990;80(2):222-6. doi: 10.1007/BF00308929.
4
Increase in diameter of the axonal initial segment is an early change in amyotrophic lateral sclerosis.
J Neurol Sci. 1992 Jul;110(1-2):114-20. doi: 10.1016/0022-510x(92)90017-f.
5
Amyotrophic lateral sclerosis: Part 1. Clinical features, pathology, and ethical issues in management.肌萎缩侧索硬化症:第1部分。临床特征、病理学及管理中的伦理问题。
Ann Neurol. 1985 Sep;18(3):271-80. doi: 10.1002/ana.410180302.
6
Degeneration and regeneration of ventral root motor fibers in amyotrophic lateral sclerosis. Morphometric studies of cervical ventral roots.
J Neurol Sci. 1982 Jul;55(1):99-115. doi: 10.1016/0022-510x(82)90173-3.
7
Beta-amyloid 42 accumulation in the lumbar spinal cord motor neurons of amyotrophic lateral sclerosis patients.β-淀粉样蛋白42在肌萎缩侧索硬化症患者腰段脊髓运动神经元中的积累。
Neurobiol Dis. 2005 Jun-Jul;19(1-2):340-7. doi: 10.1016/j.nbd.2005.01.012.
8
Degeneration of axons in spinal white matter in G93A mSOD1 mouse characterized by NFL and α-internexin immunoreactivity.由 NFL 和 α-中间丝蛋白免疫反应性特征的 G93A mSOD1 小鼠脊髓白质轴突变性。
Brain Res. 2012 Jul 17;1465:90-100. doi: 10.1016/j.brainres.2012.05.018. Epub 2012 May 17.
9
Tubular particles in a case of recurrent lymphocytic meningitis followed by amyotrophic lateral sclerosis.一例复发性淋巴细胞性脑膜炎继发肌萎缩侧索硬化症中的管状颗粒。
J Neuropathol Exp Neurol. 1975 Mar;34(2):133-47. doi: 10.1097/00005072-197503000-00002.
10
[Spinal pathology in spinal muscular atrophy in comparison with amyotrophic lateral sclerosis].[与肌萎缩侧索硬化症相比,脊髓性肌萎缩症中的脊髓病理学]
Wien Med Wochenschr. 1996;146(9-10):199-200.

引用本文的文献

1
Neurofilament Light Chain Levels in Serum and Cerebrospinal Fluid Do Not Correlate with Survival Times in Patients with Prion Disease.血清和脑脊液中的神经丝轻链水平与朊病毒病患者的生存时间无关。
Biomolecules. 2024 Dec 25;15(1):8. doi: 10.3390/biom15010008.
2
How do we get from hyperexcitability to excitotoxicity in amyotrophic lateral sclerosis?在肌萎缩侧索硬化症中,我们是如何从过度兴奋转变为兴奋毒性的?
Brain. 2024 May 3;147(5):1610-1621. doi: 10.1093/brain/awae039.
3
O-GlcNAcylation regulates neurofilament-light assembly and function and is perturbed by Charcot-Marie-Tooth disease mutations.
O-GlcNAcylation 调控神经丝轻链的组装和功能,并且其突变会受到腓骨肌萎缩症相关突变的影响。
Nat Commun. 2023 Oct 17;14(1):6558. doi: 10.1038/s41467-023-42227-0.
4
Gene Co-Expression Analysis of Multiple Brain Tissues Reveals Correlation of FAM222A Expression with Multiple Alzheimer's Disease-Related Genes.多脑区基因共表达分析揭示 FAM222A 表达与多种阿尔茨海默病相关基因的相关性。
J Alzheimers Dis. 2024;99(s2):S249-S263. doi: 10.3233/JAD-221241.
5
Autoantibodies targeting neuronal proteins as biomarkers for neurodegenerative diseases.针对神经原蛋白的自身抗体可作为神经退行性疾病的生物标志物。
Theranostics. 2022 Mar 28;12(7):3045-3056. doi: 10.7150/thno.72126. eCollection 2022.
6
Axonal spheroids in neurodegeneration.神经退行性变中的轴突球体。
Mol Cell Neurosci. 2021 Dec;117:103679. doi: 10.1016/j.mcn.2021.103679. Epub 2021 Oct 19.
7
Human Motor Neurons With SOD1-G93A Mutation Generated From CRISPR/Cas9 Gene-Edited iPSCs Develop Pathological Features of Amyotrophic Lateral Sclerosis.从CRISPR/Cas9基因编辑的诱导多能干细胞(iPSCs)产生的携带SOD1-G93A突变的人类运动神经元出现肌萎缩侧索硬化的病理特征。
Front Cell Neurosci. 2020 Nov 19;14:604171. doi: 10.3389/fncel.2020.604171. eCollection 2020.
8
Retinal Spheroids and Axon Pathology Identified in Amyotrophic Lateral Sclerosis.在肌萎缩侧索硬化症中发现了视网膜球体和轴突病变。
Invest Ophthalmol Vis Sci. 2020 Nov 2;61(13):30. doi: 10.1167/iovs.61.13.30.
9
Aluminum-Induced Synaptic Plasticity Impairment via PI3K-Akt-mTOR Signaling Pathway.铝诱导的突触可塑性损伤通过 PI3K-Akt-mTOR 信号通路。
Neurotox Res. 2020 Apr;37(4):996-1008. doi: 10.1007/s12640-020-00165-5. Epub 2020 Jan 23.
10
Sarm1 deletion suppresses TDP-43-linked motor neuron degeneration and cortical spine loss.Sarm1 缺失可抑制 TDP-43 相关运动神经元变性和皮质小棘突缺失。
Acta Neuropathol Commun. 2019 Oct 28;7(1):166. doi: 10.1186/s40478-019-0800-9.