名字有什么意义？合并还是区分肌萎缩侧索硬化症、原发性侧索硬化症、进行性肌肉萎缩症以及其他运动神经元疾病。 - Suppr

Suppr

超能文献

What's in a name? Lumping or splitting ALS, PLS, PMA, and the other motor neuron diseases.

作者信息

Rosenfeld Jeffrey, Swash Michael

出版信息

Neurology. 2006 Mar 14;66(5):624-5. doi: 10.1212/01.wnl.0000205597.62054.db.

DOI:10.1212/01.wnl.0000205597.62054.db

PMID:16534097

Abstract

摘要

相似文献

What's in a name? Lumping or splitting ALS, PLS, PMA, and the other motor neuron diseases.名字有什么意义？合并还是区分肌萎缩侧索硬化症、原发性侧索硬化症、进行性肌肉萎缩症以及其他运动神经元疾病。

Neurology. 2006 Mar 14;66(5):624-5. doi: 10.1212/01.wnl.0000205597.62054.db.

Primary lateral sclerosis, hereditary spastic paraplegia and amyotrophic lateral sclerosis: discrete entities or spectrum?原发性侧索硬化症、遗传性痉挛性截瘫和肌萎缩侧索硬化症：不同的疾病实体还是疾病谱？

Amyotroph Lateral Scler Other Motor Neuron Disord. 2005 Mar;6(1):8-16. doi: 10.1080/14660820410021267.

[Differential diagnosis and atypical subsets of amyotrophic lateral sclerosis].[肌萎缩侧索硬化症的鉴别诊断及非典型亚型]

Rev Neurol (Paris). 2006 Jun;162 Spec No 2:4S81-4S90.

Differentiation between primary lateral sclerosis and amyotrophic lateral sclerosis: examination of symptoms and signs at disease onset and during follow-up.原发性侧索硬化与肌萎缩侧索硬化的鉴别：疾病发作时及随访期间症状和体征的检查

Arch Neurol. 2007 Feb;64(2):232-6. doi: 10.1001/archneur.64.2.232.

Clinical features that distinguish PLS, upper motor neuron-dominant ALS, and typical ALS.区分进行性延髓麻痹（PLS）、上运动神经元为主型肌萎缩侧索硬化症（ALS）和典型ALS的临床特征。

Neurology. 2009 Jun 2;72(22):1948-52. doi: 10.1212/WNL.0b013e3181a8269b.

Hemiplegic ALS: Mills syndrome.偏瘫型肌萎缩侧索硬化症：米尔斯综合征。

Neurology. 2005 Jun 14;64(11):1984-5. doi: 10.1212/01.WNL.0000163995.62871.A4.

Overview of motor neuron disease: classification and nomenclature.运动神经元病概述：分类与命名

Clin Neurosci. 1995;3(6):323-6.

Amyotrophic lateral sclerosis and primary lateral sclerosis: The role of diffusion tensor imaging and other advanced MR-based techniques as objective upper motor neuron markers.肌萎缩侧索硬化症和原发性侧索硬化症：扩散张量成像及其他基于磁共振成像的先进技术作为客观上运动神经元标志物的作用。

Ann N Y Acad Sci. 2005 Dec;1064:61-77. doi: 10.1196/annals.1340.013.

What's in a name? Amyotrophic lateral sclerosis, motor neuron disease, and allelic heterogeneity.名字里有什么？肌萎缩侧索硬化症、运动神经元病与等位基因异质性。

Ann Neurol. 1998 Jun;43(6):691-4. doi: 10.1002/ana.410430602.

[Amyotrophic lateral sclerosis: differential diagnosis and frontier forms].[肌萎缩侧索硬化症：鉴别诊断与前沿形式]

Rev Neurol (Paris). 2006 Jun;162 Spec No 2:4S67-4S80.

引用本文的文献

Motor phenotypes of amyotrophic lateral sclerosis - a three-determinant anatomical classification based on the region of onset, propagation of motor symptoms, and the degree of upper and lower motor neuron dysfunction.肌萎缩侧索硬化症的运动表型——一种基于发病部位、运动症状传播以及上下运动神经元功能障碍程度的三要素解剖学分类。

Neurol Res Pract. 2025 Apr 28;7(1):27. doi: 10.1186/s42466-025-00389-w.

Unraveling the complex interplay between genes, environment, and climate in ALS.揭示 ALS 中基因、环境和气候之间复杂的相互作用。

EBioMedicine. 2022 Jan;75:103795. doi: 10.1016/j.ebiom.2021.103795. Epub 2021 Dec 30.

Predicting the severity of motor neuron disease progression using electronic health record data with a cloud computing Big Data approach.使用云计算大数据方法通过电子健康记录数据预测运动神经元疾病进展的严重程度。

IEEE Symp Comput Intell Bioinforma Comput Biol Proc. 2014 May;2014. doi: 10.1109/CIBCB.2014.6845506.

Challenges in the Understanding and Treatment of Amyotrophic Lateral Sclerosis/Motor Neuron Disease.肌萎缩侧索硬化症/运动神经元病理解与治疗中的挑战

Neurotherapeutics. 2015 Apr;12(2):317-25. doi: 10.1007/s13311-014-0332-8.

Quantifying disease progression in amyotrophic lateral sclerosis.定量肌萎缩侧索硬化症的疾病进展。

Ann Neurol. 2014 Nov;76(5):643-57. doi: 10.1002/ana.24273. Epub 2014 Sep 30.

Latent cluster analysis of ALS phenotypes identifies prognostically differing groups.ALS 表型的潜在聚类分析确定了预后不同的组。

PLoS One. 2009 Sep 22;4(9):e7107. doi: 10.1371/journal.pone.0007107.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验