Amyotrophic lateral sclerosis—Motor neuron disease with a wide clinical and genetic spectrum
Author:
Publisher
Springer Science and Business Media LLC
Subject
Psychiatry and Mental health,Neurology (clinical),Neurology,General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s00115-023-01479-3.pdf
Reference29 articles.
1. Andrews JA, Jackson CE, Heiman-Patterson TD et al (2020) Real-world evidence of riluzole effectiveness in treating amyotrophic lateral sclerosis. Amyotroph Lateral Scler Frontotemporal Degener 21(7–8):509–518
2. Aust E, Boentert M, Brenner D et al (2022) Amyotrophe Lateralsklerose und andere Motoneuronerkrankungen. Pathophysiologie, Diagnostik und Therapie, 1. Aufl. Kohlhammer, Stuttgart
3. Beeldman E, Raaphorst J, Klein Twennaar M et al (2016) The cognitive profile of ALS: a systematic review and meta-analysis update. J Neurol Neurosurg Psychiatry 87(6):611–619
4. Brettschneider J, Del Tredici K, Toledo JB et al (2013) Stages of pTDP-43 pathology in amyotrophic lateral sclerosis. Ann Neurol 74(1):20–38
5. Brooks BR, Miller RG, Swash M et al (2000) El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis. Amyotroph Lateral Scler Other Motor Neuron Disord 1(5):293–299
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