• 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

相似文献

1
Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update.额颞叶变性神经病理亚型的命名与分类学：更新版
Acta Neuropathol. 2010 Jan;119(1):1-4. doi: 10.1007/s00401-009-0612-2. Epub 2009 Nov 19.
2
Novel types of frontotemporal lobar degeneration: beyond tau and TDP-43.新型额颞叶痴呆：超越 tau 和 TDP-43。
J Mol Neurosci. 2011 Nov;45(3):402-8. doi: 10.1007/s12031-011-9551-1. Epub 2011 May 21.
3
Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations.额颞叶变性神经病理学亚型的命名：共识推荐
Acta Neuropathol. 2009 Jan;117(1):15-8. doi: 10.1007/s00401-008-0460-5. Epub 2008 Nov 18.
4
Neuronal cytoplasmic inclusions in tau, TDP-43, and FUS molecular subtypes of frontotemporal lobar degeneration share similar spatial patterns.额颞叶痴呆的tau、TDP-43和FUS分子亚型中的神经元胞质内含物具有相似的空间模式。
Folia Neuropathol. 2017;55(3):185-192. doi: 10.5114/fn.2017.70482.
5
Frontotemporal lobar degeneration: new understanding brings new approaches.额颞叶变性：新的认识带来新的方法。
Neuroimaging Clin N Am. 2012 Feb;22(1):83-97, viii. doi: 10.1016/j.nic.2011.11.009.
6
What's in a name? Neuronal intermediate filament inclusion disease (NIFID), frontotemporal lobar degeneration-intermediate filament (FTLD-IF) or frontotemporal lobar degeneration-fused in sarcoma (FTLD-FUS)?名字意味着什么？神经元中间丝包涵体病（NIFID）、额颞叶痴呆-中间丝型（FTLD-IF）还是额颞叶痴呆-肉瘤融合基因型（FTLD-FUS）？
J Neurol Neurosurg Psychiatry. 2011 Dec;82(12):1412-4. doi: 10.1136/jnnp.2010.220947. Epub 2010 Nov 8.
7
Basophilic inclusions and neuronal intermediate filament inclusions in amyotrophic lateral sclerosis and frontotemporal lobar degeneration.肌萎缩侧索硬化症和额颞叶痴呆中的嗜碱性包涵体和神经元中间丝包涵体
Neuropathology. 2014 Dec;34(6):589-95. doi: 10.1111/neup.12119. Epub 2014 Mar 27.
8
Phenotypic variability within the inclusion body spectrum of basophilic inclusion body disease and neuronal intermediate filament inclusion disease in frontotemporal lobar degenerations with FUS-positive inclusions.在伴有 FUS 阳性包涵体的额颞叶变性中，嗜碱性包涵体病和神经元中间丝包涵体病的包涵体谱内的表型变异性。
J Neuropathol Exp Neurol. 2012 Sep;71(9):795-805. doi: 10.1097/NEN.0b013e318266efb1.
9
Unpicking frontotemporal lobar degeneration.剖析额颞叶痴呆
Brain. 2011 Sep;134(Pt 9):2453-5. doi: 10.1093/brain/awr176. Epub 2011 Aug 22.
10
The clinical and neuroanatomical phenotype of FUS associated frontotemporal lobar degeneration.与FUS相关的额颞叶痴呆的临床和神经解剖学表型。
J Neurol Neurosurg Psychiatry. 2011 Dec;82(12):1405-7. doi: 10.1136/jnnp.2010.214437. Epub 2010 Jul 16.

引用本文的文献

1
Incidence and Prevalence of Frontotemporal Dementia: A Systematic Review and Meta-Analysis.额颞叶痴呆的发病率和患病率：一项系统评价与荟萃分析
JAMA Neurol. 2025 Sep 8. doi: 10.1001/jamaneurol.2025.3307.
2
AI-driven fusion of multimodal data for Alzheimer's disease biomarker assessment.用于阿尔茨海默病生物标志物评估的多模态数据的人工智能驱动融合。
Nat Commun. 2025 Aug 11;16(1):7407. doi: 10.1038/s41467-025-62590-4.
3
Brain transcriptomics highlight abundant gene expression and splicing alterations in non-neuronal cells in aFTLD-U.脑转录组学揭示了进行性核上性麻痹伴额颞叶痴呆（aFTLD-U）中非神经元细胞中丰富的基因表达和剪接改变。
Acta Neuropathol. 2025 Aug 10;150(1):17. doi: 10.1007/s00401-025-02919-x.
4
Corticobasal degeneration preceded by cognitive impairment and apathy: An autopsy case report.以认知障碍和淡漠为前驱症状的皮质基底节变性：一例尸检病例报告。
PCN Rep. 2025 Aug 3;4(3):e70174. doi: 10.1002/pcn5.70174. eCollection 2025 Sep.
5
Methylome analysis of FTLD patients with TDP-43 pathology identifies epigenetic signatures specific to pathological subtypes.对患有TDP-43病理学的额颞叶痴呆（FTLD）患者进行甲基化组分析，确定了特定于病理亚型的表观遗传特征。
Mol Neurodegener. 2025 Jul 6;20(1):80. doi: 10.1186/s13024-025-00869-2.
6
Multiparametric MRI-based biomarkers in the non-fluent and semantic variants of primary progressive aphasia.基于多参数磁共振成像的原发性进行性失语非流利型和语义型变体生物标志物
J Neurol. 2025 Jul 2;272(8):490. doi: 10.1007/s00415-025-13215-9.
7
PGRN Counteracts the Associations of Abnormal Tau Proteins with Neurodegeneration and Cognitive Decline in Non-demented Adults: A Longitudinal Study.前颗粒蛋白对抗异常 Tau 蛋白与非痴呆成年人神经退行性变和认知衰退的关联：一项纵向研究。
Mol Neurobiol. 2025 Jun 25. doi: 10.1007/s12035-025-05154-3.
8
The mechanisms underlying TDP-43-associated neurodegeneration in Alzheimer's disease and related dementias.阿尔茨海默病及相关痴呆中与TDP-43相关的神经退行性变的潜在机制。
Mol Psychiatry. 2025 Jun 25. doi: 10.1038/s41380-025-03089-8.
9
Interrogating the plasma proteome of repetitive head impact exposure and chronic traumatic encephalopathy.探究重复性头部撞击暴露与慢性创伤性脑病的血浆蛋白质组。
Mol Neurodegener. 2025 Jun 16;20(1):71. doi: 10.1186/s13024-025-00860-x.
10
Protein Pathologies in Oligodendroglia in Neurodegenerative Diseases.神经退行性疾病中少突胶质细胞的蛋白质病理学
Adv Neurobiol. 2025;43:407-432. doi: 10.1007/978-3-031-87919-7_14.

本文引用的文献

1
Absence of FUS-immunoreactive pathology in frontotemporal dementia linked to chromosome 3 (FTD-3) caused by mutation in the CHMP2B gene.由CHMP2B基因突变引起的与3号染色体相关的额颞叶痴呆（FTD-3）中不存在FUS免疫反应性病理改变。
Acta Neuropathol. 2009 Nov;118(5):719-20. doi: 10.1007/s00401-009-0593-1. Epub 2009 Oct 21.
2
FUS pathology in basophilic inclusion body disease.脑基底核中铁颗粒沉积症中的 FUS 病理学。
Acta Neuropathol. 2009 Nov;118(5):617-27. doi: 10.1007/s00401-009-0598-9. Epub 2009 Oct 15.
3
Analysis of FUS gene mutation in familial amyotrophic lateral sclerosis within an Italian cohort.意大利队列中家族性肌萎缩侧索硬化症的FUS基因突变分析
Neurology. 2009 Oct 13;73(15):1180-5. doi: 10.1212/WNL.0b013e3181bbff05. Epub 2009 Sep 9.
4
A new subtype of frontotemporal lobar degeneration with FUS pathology.具有 FUS 病理学特征的额颞叶变性的一个新亚型。
Brain. 2009 Nov;132(Pt 11):2922-31. doi: 10.1093/brain/awp214. Epub 2009 Aug 11.
5
Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease.神经元中间丝包涵体病中丰富的 FUS 免疫反应性病理学。
Acta Neuropathol. 2009 Nov;118(5):605-16. doi: 10.1007/s00401-009-0581-5. Epub 2009 Aug 9.
6
TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea.与额颞叶痴呆、核上性凝视麻痹和舞蹈症相关的TARDBP变异
Mov Disord. 2009 Sep 15;24(12):1843-7. doi: 10.1002/mds.22697.
7
Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6.FUS（一种RNA加工蛋白）中的突变会导致6型家族性肌萎缩侧索硬化症。
Science. 2009 Feb 27;323(5918):1208-1211. doi: 10.1126/science.1165942.
8
Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis.16号染色体上FUS/TLS基因的突变会导致家族性肌萎缩侧索硬化症。
Science. 2009 Feb 27;323(5918):1205-8. doi: 10.1126/science.1166066.
9
The role of CHMP2B in frontotemporal dementia.CHMP2B在额颞叶痴呆中的作用。
Biochem Soc Trans. 2009 Feb;37(Pt 1):208-12. doi: 10.1042/BST0370208.
10
Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations.额颞叶变性神经病理学亚型的命名：共识推荐
Acta Neuropathol. 2009 Jan;117(1):15-8. doi: 10.1007/s00401-008-0460-5. Epub 2008 Nov 18.

Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update.

作者信息

Mackenzie Ian R A, Neumann Manuela, Bigio Eileen H, Cairns Nigel J, Alafuzoff Irina, Kril Jillian, Kovacs Gabor G, Ghetti Bernardino, Halliday Glenda, Holm Ida E, Ince Paul G, Kamphorst Wouter, Revesz Tamas, Rozemuller Annemieke J M, Kumar-Singh Samir, Akiyama Haruhiko, Baborie Atik, Spina Salvatore, Dickson Dennis W, Trojanowski John Q, Mann David M A

机构信息

Department of Pathology and Laboratory Medicine, Vancouver General Hospital and University of British Columbia, Vancouver, BC, Canada.

出版信息

Acta Neuropathol. 2010 Jan;119(1):1-4. doi: 10.1007/s00401-009-0612-2. Epub 2009 Nov 19.

DOI:10.1007/s00401-009-0612-2
PMID:19924424
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2799633/
Abstract
摘要