Prognostic role of slow vital capacity in amyotrophic lateral sclerosis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Clinical Neurology,Neurology
Link
http://link.springer.com/content/pdf/10.1007/s00415-020-09751-1.pdf
Reference38 articles.
1. van Es MA, Hardiman O, Chio A et al (2017) Amyotrophic lateral sclerosis. Lancet 390:2084–2098. https://doi.org/10.1016/S0140-6736(17)31287-4
2. Amyotrophic Lateral Sclerosis (ALS) Fact Sheet|National Institute of Neurological Disorders and Stroke. https://www.ninds.nih.gov/Disorders/Patient-Caregiver-Education/Fact-Sheets/Amyotrophic-Lateral-Sclerosis-ALS-Fact-Sheet. Accessed 20 Mar 2019
3. Pinto S, de Carvalho M (2015) The R of ALSFRS-R: does it really mirror functional respiratory involvement in amyotrophic lateral sclerosis? Amyotroph Lateral Scler Front Degener 16:120–123. https://doi.org/10.3109/21678421.2014.952641
4. Lenglet T, Lacomblez L, Abitbol JL et al (2014) A phase II–III trial of olesoxime in subjects with amyotrophic lateral sclerosis. Eur J Neurol 21:529–536. https://doi.org/10.1111/ene.12344
5. Czaplinski A, Yen AA, Appel SH (2006) Forced vital capacity (FVC) as an indicator of survival and disease progression in an ALS clinic population. J Neurol Neurosurg Psychiatry 77:390–392. https://doi.org/10.1136/jnnp.2005.072660
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