• 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

Human cerebral evolution and the clinical syndrome of amyotrophic lateral sclerosis.

作者信息

Henderson Robert D, Garton Fleur C, Kiernan Matthew C, Turner Martin R, Eisen Andrew

机构信息

Department of Neurology, Royal Brisbane and Women's Hospital, Brisbane, Queensland, Australia.

Institute for Molecular Bioscience, University of Queensland, Brisbane, Queensland, Australia.

出版信息

J Neurol Neurosurg Psychiatry. 2019 May;90(5):570-575. doi: 10.1136/jnnp-2017-317245. Epub 2018 Apr 17.

DOI:10.1136/jnnp-2017-317245
PMID:29666205
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6581076/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c54/6581076/d24a20f83261/jnnp-2017-317245f03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c54/6581076/c4ba9409e57c/jnnp-2017-317245f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c54/6581076/f3f39006dd88/jnnp-2017-317245f02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c54/6581076/d24a20f83261/jnnp-2017-317245f03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c54/6581076/c4ba9409e57c/jnnp-2017-317245f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c54/6581076/f3f39006dd88/jnnp-2017-317245f02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c54/6581076/d24a20f83261/jnnp-2017-317245f03.jpg

相似文献

1
Human cerebral evolution and the clinical syndrome of amyotrophic lateral sclerosis.人类大脑进化与肌萎缩侧索硬化症临床综合征
J Neurol Neurosurg Psychiatry. 2019 May;90(5):570-575. doi: 10.1136/jnnp-2017-317245. Epub 2018 Apr 17.
2
Trauma, axonal injury, and amyotrophic lateral sclerosis: a clinical correlate of a neuropharmacologic model.
Clin Neuropharmacol. 1995 Jun;18(3):273-6. doi: 10.1097/00002826-199506000-00008.
3
Motor neuron disease (amyotrophic lateral sclerosis) arising from longstanding primary lateral sclerosis.源于长期原发性侧索硬化症的运动神经元病(肌萎缩性侧索硬化症)
J Neurol Neurosurg Psychiatry. 1995 Jun;58(6):742-4. doi: 10.1136/jnnp.58.6.742.
4
Atypical astrocytes and Rosenthal fibers in a case of amyotrophic lateral sclerosis associated with a cerebral glioblastoma multiforme.
Acta Neuropathol. 1975;31(1):29-34. doi: 10.1007/BF00696884.
5
A case of Mills' syndrome: initially characterized by one cerebral hemisphere atrophy and decreased brain metabolism then evolving into amyotrophic lateral sclerosis.一例米尔斯综合征:最初表现为一侧大脑半球萎缩和脑代谢降低,随后发展为肌萎缩侧索硬化症。
Neurol Sci. 2024 Mar;45(3):1311-1313. doi: 10.1007/s10072-023-07234-5. Epub 2023 Dec 4.
6
Amyotrophic lateral sclerosis. Inclusion bodies in a case of the classic sporadic form.
Ann Clin Lab Sci. 1975 Jan-Feb;5(1):38-44.
7
The role of mitochondria in amyotrophic lateral sclerosis.线粒体在肌萎缩侧索硬化症中的作用。
Neurosci Lett. 2019 Sep 25;710:132933. doi: 10.1016/j.neulet.2017.06.052. Epub 2017 Jun 30.
8
Amyotrophic lateral sclerosis: a phylogenetic disease of the corticomotoneuron? Comments on the hypothesis.肌萎缩侧索硬化症:一种皮质运动神经元的系统发育疾病?对该假说的评论。
Muscle Nerve. 1992 Feb;15(2):226-8. doi: 10.1002/mus.880150217.
9
Frontotemporal dementia with motor neuron disease (amyotrophic lateral sclerosis with dementia).
Neuropathology. 2000 Mar;20(1):68-75. doi: 10.1046/j.1440-1789.2000.00272.x.
10
Clinico-pathological features in amyotrophic lateral sclerosis with expansions in C9ORF72.伴有 C9ORF72 基因扩增的肌萎缩侧索硬化症的临床病理特征。
Brain. 2012 Mar;135(Pt 3):751-64. doi: 10.1093/brain/awr365.

引用本文的文献

1
Longitudinal assessment of cortical motor function in amyotrophic lateral sclerosis.肌萎缩侧索硬化症皮质运动功能的纵向评估
Sci Rep. 2025 May 15;15(1):16978. doi: 10.1038/s41598-025-01570-6.
2
Asymmetry in amyotrophic lateral sclerosis: Clinical, neuroimaging and histological observations.肌萎缩侧索硬化症中的不对称性:临床、神经影像学和组织学观察。
Brain. 2025 Aug 1;148(8):2605-2615. doi: 10.1093/brain/awaf121.
3
Drug repurposing in amyotrophic lateral sclerosis (ALS).肌萎缩侧索硬化症(ALS)中的药物重新利用。

本文引用的文献

1
The evolution of modern human brain shape.现代人脑形状的演变。
Sci Adv. 2018 Jan 24;4(1):eaao5961. doi: 10.1126/sciadv.aao5961. eCollection 2018 Jan.
2
Unraveling the Role of RNA Mediated Toxicity of Repeats in C9-FTD/ALS.解析C9型额颞叶痴呆/肌萎缩侧索硬化症中RNA介导的重复序列毒性作用
Front Neurosci. 2017 Dec 15;11:711. doi: 10.3389/fnins.2017.00711. eCollection 2017.
3
Clustering of Neuropsychiatric Disease in First-Degree and Second-Degree Relatives of Patients With Amyotrophic Lateral Sclerosis.肌萎缩侧索硬化症患者一级和二级亲属中神经精神疾病的聚集情况。
Expert Opin Drug Discov. 2025 Apr;20(4):447-464. doi: 10.1080/17460441.2025.2474661. Epub 2025 Mar 7.
4
A novel muscle network approach for objective assessment and profiling of bulbar involvement in ALS.一种用于客观评估和分析肌萎缩侧索硬化症延髓受累情况的新型肌肉网络方法。
Front Neurosci. 2025 Jan 10;18:1491997. doi: 10.3389/fnins.2024.1491997. eCollection 2024.
5
ALS/FTD: Evolution, Aging, and Cellular Metabolic Exhaustion.肌萎缩侧索硬化症/额颞叶痴呆:演变、衰老与细胞代谢耗竭
Front Neurol. 2022 May 27;13:890203. doi: 10.3389/fneur.2022.890203. eCollection 2022.
6
Tackling clinical heterogeneity across the amyotrophic lateral sclerosis-frontotemporal dementia spectrum using a transdiagnostic approach.采用跨诊断方法应对肌萎缩侧索硬化症 - 额颞叶痴呆谱系中的临床异质性。
Brain Commun. 2021 Oct 23;3(4):fcab257. doi: 10.1093/braincomms/fcab257. eCollection 2021.
7
Cortical Excitability across the ALS Clinical Motor Phenotypes.肌萎缩侧索硬化症临床运动表型中的皮质兴奋性
Brain Sci. 2021 May 28;11(6):715. doi: 10.3390/brainsci11060715.
8
Improving clinical trial outcomes in amyotrophic lateral sclerosis.提高肌萎缩侧索硬化症临床试验的结果。
Nat Rev Neurol. 2021 Feb;17(2):104-118. doi: 10.1038/s41582-020-00434-z. Epub 2020 Dec 18.
JAMA Neurol. 2017 Dec 1;74(12):1425-1430. doi: 10.1001/jamaneurol.2017.2699.
4
Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis.跨种族荟萃分析确定了GPX3-TNIP1基因座与肌萎缩侧索硬化症的关联。
Nat Commun. 2017 Sep 20;8(1):611. doi: 10.1038/s41467-017-00471-1.
5
Detection of long repeat expansions from PCR-free whole-genome sequence data.从无 PCR 全基因组序列数据中检测长重复扩展。
Genome Res. 2017 Nov;27(11):1895-1903. doi: 10.1101/gr.225672.117. Epub 2017 Sep 8.
6
Whole exome sequencing and DNA methylation analysis in a clinical amyotrophic lateral sclerosis cohort.临床肌萎缩侧索硬化症队列中的全外显子组测序和DNA甲基化分析
Mol Genet Genomic Med. 2017 Jun 12;5(4):418-428. doi: 10.1002/mgg3.302. eCollection 2017 Jul.
7
Cortical influences drive amyotrophic lateral sclerosis.皮层影响导致肌萎缩侧索硬化。
J Neurol Neurosurg Psychiatry. 2017 Nov;88(11):917-924. doi: 10.1136/jnnp-2017-315573. Epub 2017 Jul 14.
8
Deeply divergent archaic mitochondrial genome provides lower time boundary for African gene flow into Neanderthals.高度分化的古老线粒体基因组为非洲基因流入尼安德特人提供了更低的时间边界。
Nat Commun. 2017 Jul 4;8:16046. doi: 10.1038/ncomms16046.
9
The Evolution of Lateralized Brain Circuits.大脑侧化回路的进化
Front Psychol. 2017 Jun 16;8:1021. doi: 10.3389/fpsyg.2017.01021. eCollection 2017.
10
Pathology of callosal damage in ALS: An , 7 T diffusion tensor MRI study.肌萎缩侧索硬化症胼胝体损伤的病理学:一项7T扩散张量磁共振成像研究
Neuroimage Clin. 2017 Apr 30;15:200-208. doi: 10.1016/j.nicl.2017.04.024. eCollection 2017.