• 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

Proposed criteria for familial amyotrophic lateral sclerosis.

作者信息

Byrne Susan, Bede Peter, Elamin Marwa, Kenna Kevin, Lynch Catherine, McLaughlin Russell, Hardiman Orla

机构信息

TCIN, Trinity College, Dublin, Ireland.

出版信息

Amyotroph Lateral Scler. 2011 May;12(3):157-9. doi: 10.3109/17482968.2010.545420. Epub 2011 Jan 5.

DOI:10.3109/17482968.2010.545420
PMID:21208036
Abstract
摘要

相似文献

1
Proposed criteria for familial amyotrophic lateral sclerosis.家族性肌萎缩侧索硬化症的拟议标准。
Amyotroph Lateral Scler. 2011 May;12(3):157-9. doi: 10.3109/17482968.2010.545420. Epub 2011 Jan 5.
2
An unusual case of familial ALS and cerebellar ataxia.
Amyotroph Lateral Scler. 2010 Dec;11(6):568-70. doi: 10.3109/17482961003636874. Epub 2010 Jun 14.
3
Genetic aspects of amyotrophic lateral sclerosis.肌萎缩侧索硬化症的遗传学方面
Adv Neurol. 2002;88:21-32.
4
Heterogeneity of pathological processes in amyotrophic lateral sclerosis?
J Neurol Neurosurg Psychiatry. 2011 Aug;82(8):827. doi: 10.1136/jnnp.2011.241521. Epub 2011 Jun 2.
5
A novel SOD1 mutation in a young amyotrophic lateral sclerosis patient with a very slowly progressive clinical course.一位年轻的肌萎缩侧索硬化症患者具有非常缓慢进展的临床病程,存在一种新型 SOD1 突变。
Muscle Nerve. 2010 Oct;42(4):596-7. doi: 10.1002/mus.21750.
6
Racing against the clock: recognizing, differentiating, diagnosing, and referring the amyotrophic lateral sclerosis patient.与时间赛跑:识别、鉴别、诊断及转诊肌萎缩侧索硬化症患者。
Ann Neurol. 2009 Jan;65 Suppl 1:S10-6. doi: 10.1002/ana.21545.
7
[Genetics of amyotrophic lateral sclerosis].[肌萎缩侧索硬化症的遗传学]
Zh Nevrol Psikhiatr Im S S Korsakova. 2001;101(3):54-63.
8
Primary lateral sclerosis as a phenotypic manifestation of familial ALS.原发性侧索硬化作为家族性肌萎缩侧索硬化的一种表型表现。
Neurology. 2005 May 24;64(10):1778-9. doi: 10.1212/01.WNL.0000162033.47893.F7.
9
A4V superoxide dismutase mutation in apparently sporadic ALS resembling neuralgic amyotrophy.
Amyotroph Lateral Scler. 2006 Mar;7(1):61-3. doi: 10.1080/14660820500467009.
10
Amyotrophic lateral sclerosis: pathogenesis.肌萎缩侧索硬化症:发病机制
Acta Neurol Belg. 2000 Sep;100(3):181-7.

引用本文的文献

1
Whole blood transcriptome profile identifies motor neurone disease RNA biomarker signatures.全血转录组图谱鉴定运动神经元病的RNA生物标志物特征。
Exp Biol Med (Maywood). 2025 Jan 8;249:10401. doi: 10.3389/ebm.2024.10401. eCollection 2024.
2
Efficacy of pain management strategies in adults with Amyotrophic Lateral Sclerosis (ALS): A Systematic Review.成人肌萎缩侧索硬化症(ALS)疼痛管理策略的疗效:系统评价。
Neurol Sci. 2024 Dec;45(12):5591-5604. doi: 10.1007/s10072-024-07643-0. Epub 2024 Jul 5.
3
Identification of a pathogenic mutation in in patients with amyotrophic lateral sclerosis.
肌萎缩侧索硬化症患者中致病突变的鉴定。
J Neurol Neurosurg Psychiatry. 2025 Jan 16;96(2):132-139. doi: 10.1136/jnnp-2024-333834.
4
Genetics screening in an Italian cohort of patients with Amyotrophic Lateral Sclerosis: the importance of early testing and its implication.意大利肌萎缩侧索硬化症患者的遗传学筛查:早期检测的重要性及其意义。
J Neurol. 2024 Apr;271(4):1921-1936. doi: 10.1007/s00415-023-12142-x. Epub 2023 Dec 19.
5
Estimated Familial Amyotrophic Lateral Sclerosis Proportion: A Literature Review and Meta-analysis.估计的家族性肌萎缩侧索硬化症比例:一项文献综述与荟萃分析
Neurol Genet. 2023 Nov 30;9(6):e200109. doi: 10.1212/NXG.0000000000200109. eCollection 2023 Dec.
6
Epidemiologic Trends of Amyotrophic Lateral Sclerosis in Ireland, 1996-2021.爱尔兰肌萎缩侧索硬化症的流行病学趋势,1996-2021 年。
Neurology. 2023 Nov 7;101(19):e1905-e1912. doi: 10.1212/WNL.0000000000207797. Epub 2023 Sep 25.
7
Cognitive and neuropsychiatric endophenotypes in amyotrophic lateral sclerosis.肌萎缩侧索硬化症中的认知和神经精神内表型
Brain Commun. 2023 May 19;5(3):fcad166. doi: 10.1093/braincomms/fcad166. eCollection 2023.
8
Genetic variability in sporadic amyotrophic lateral sclerosis.散发性肌萎缩侧索硬化症的遗传变异性。
Brain. 2023 Sep 1;146(9):3760-3769. doi: 10.1093/brain/awad120.
9
Identifying and predicting amyotrophic lateral sclerosis clinical subgroups: a population-based machine-learning study.基于人群的机器学习研究:识别和预测肌萎缩侧索硬化临床亚组。
Lancet Digit Health. 2022 May;4(5):e359-e369. doi: 10.1016/S2589-7500(21)00274-0. Epub 2022 Mar 24.
10
ALS in Finland: Major Genetic Variants and Clinical Characteristics of Patients With and Without the Hexanucleotide Repeat Expansion.芬兰的肌萎缩侧索硬化症:有和没有六核苷酸重复扩增的患者的主要基因变异及临床特征
Neurol Genet. 2022 Mar 14;8(2):e665. doi: 10.1212/NXG.0000000000000665. eCollection 2022 Apr.