Biochemical parameters in determination of nutritional status in amyotrophic lateral sclerosis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Psychiatry and Mental health,Clinical Neurology,Dermatology,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/s10072-019-04201-x.pdf
Reference43 articles.
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2. Gordon PH (2013) Amyotrophic lateral sclerosis: an update for 2013 clinical features, pathophysiology, management and therapeutic trials. Aging Dis 4(5):295–310. https://doi.org/10.14336/AD.2013.0400295
3. Chiò A, Calvo A, Moglia C, Mazzini L, Mora G, group Ps (2011) Phenotypic heterogeneity of amyotrophic lateral sclerosis: a population based study. J Neurol Neurosurg Psychiatry 82(7):740–746. https://doi.org/10.1136/jnnp.2010.235952
4. GROUP WGOBOTEM-AS (2017) Open-label 24-week extension study of edaravone (MCI-186) in amyotrophic lateral sclerosis. Amyotroph Lateral Scler Frontotemporal Degener 18(sup1):55–63. https://doi.org/10.1080/21678421.2017.1364269
5. Rothstein JD (2017) Edaravone: a new drug approved for ALS. Cell 171(4):725. https://doi.org/10.1016/j.cell.2017.10.011
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