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本文引用的文献

1
Correlation between pyramidal tract degeneration and widespread white matter involvement in amyotrophic lateral sclerosis: a study with tractography and diffusion-tensor imaging.肌萎缩侧索硬化症中锥体束变性与广泛白质受累之间的相关性:一项基于纤维束成像和扩散张量成像的研究
Amyotroph Lateral Scler. 2009 Oct-Dec;10(5-6):288-94. doi: 10.3109/17482960802651717.
2
Structural and metabolic changes in the brain of patients with upper motor neuron disorders: a multiparametric MRI study.上运动神经元疾病患者大脑的结构和代谢变化:一项多参数MRI研究。
Amyotroph Lateral Scler. 2009 Oct-Dec;10(5-6):269-79. doi: 10.3109/17482960902777339.
3
MRI-based functional neuroimaging in ALS: an update.肌萎缩侧索硬化症中基于磁共振成像的功能神经影像学:最新进展
Amyotroph Lateral Scler. 2009 Oct-Dec;10(5-6):258-68. doi: 10.3109/17482960802353504.
4
Mutations of FUS gene in sporadic amyotrophic lateral sclerosis.FUS 基因在散发性肌萎缩侧索硬化症中的突变。
J Med Genet. 2010 Mar;47(3):190-4. doi: 10.1136/jmg.2009.071027. Epub 2009 Oct 26.
5
Genetics of motor neuron disorders: new insights into pathogenic mechanisms.运动神经元疾病的遗传学:对致病机制的新见解
Nat Rev Genet. 2009 Nov;10(11):769-82. doi: 10.1038/nrg2680. Epub 2009 Oct 13.
6
Broad clinical phenotypes associated with TAR-DNA binding protein (TARDBP) mutations in amyotrophic lateral sclerosis.与肌萎缩侧索硬化症相关的 TAR-DNA 结合蛋白 (TARDBP) 突变的广泛临床表型。
Neurogenetics. 2010 May;11(2):217-25. doi: 10.1007/s10048-009-0218-9. Epub 2009 Sep 17.
7
Mutations in FUS cause FALS and SALS in French and French Canadian populations.在法国和法裔加拿大人群中,FUS基因的突变会导致家族性肌萎缩侧索硬化症(FALS)和散发性肌萎缩侧索硬化症(SALS)。
Neurology. 2009 Oct 13;73(15):1176-9. doi: 10.1212/WNL.0b013e3181bbfeef. Epub 2009 Sep 9.
8
ALS motor phenotype heterogeneity, focality, and spread: deconstructing motor neuron degeneration.肌萎缩侧索硬化症的运动表型异质性、局灶性和扩散:解析运动神经元变性
Neurology. 2009 Sep 8;73(10):805-11. doi: 10.1212/WNL.0b013e3181b6bbbd.
9
Changes of resting state brain networks in amyotrophic lateral sclerosis.肌萎缩侧索硬化症患者静息态脑网络的变化
Exp Neurol. 2009 May;217(1):147-53. doi: 10.1016/j.expneurol.2009.01.025. Epub 2009 Feb 12.
10
Quantitative diffusion tensor imaging in amyotrophic lateral sclerosis: revisited.定量弥散张量成像在肌萎缩侧索硬化症中的再研究。
Hum Brain Mapp. 2009 Nov;30(11):3657-75. doi: 10.1002/hbm.20794.

肌萎缩侧索硬化症的神经影像学的现在和未来。

The present and the future of neuroimaging in amyotrophic lateral sclerosis.

机构信息

Institute of Experimental Neurology, University Hospital San Raffaele, Milan, Italy.

出版信息

AJNR Am J Neuroradiol. 2010 Nov;31(10):1769-77. doi: 10.3174/ajnr.A2043. Epub 2010 Apr 1.

DOI:10.3174/ajnr.A2043
PMID:20360339
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7964007/
Abstract

In patients with ALS, conventional MR imaging is frequently noninformative, and its use has been restricted to excluding other conditions that can mimic ALS. Conversely, the extensive application of modern MR imaging-based techniques to the study of ALS has undoubtedly improved our understanding of disease pathophysiology and is likely to have a role in the identification of potential biomarkers of disease progression. This review summarizes how new MR imaging technology is changing dramatically our understanding of the factors associated with ALS evolution and highlights the reasons why it should be used more extensively in studies of disease progression, including clinical trials.

摘要

在 ALS 患者中,常规磁共振成像通常没有信息,其应用仅限于排除其他可能模仿 ALS 的疾病。相反,广泛应用现代基于磁共振成像的技术研究 ALS,无疑提高了我们对疾病病理生理学的认识,并可能在确定疾病进展的潜在生物标志物方面发挥作用。这篇综述总结了新的磁共振成像技术如何极大地改变了我们对与 ALS 进展相关因素的认识,并强调了为什么它应该更广泛地用于疾病进展的研究,包括临床试验。