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Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|December 9, 2014
Deficits in sentence expression in amyotrophic lateral sclerosisSharon Ash, Christopher Olm, Corey T McMillan, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|October 30, 2015
Pain in amyotrophic lateral sclerosis: Patient and physician perspectives and practicesHelen E Stephens, Erik Lehman, Divisha Raheja, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|April 15, 2016
A mapping review of international guidance on the management and care of amyotrophic lateral sclerosis (ALS)Astrid I W A Janssens, Marijke Ruytings, Ammar Al-Chalabi, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|February 12, 2016
The ALSFRS as an outcome measure in therapeutic trials and its relationship to symptom onsetMalcolm Proudfoot, Ashley Jones, Kevin Talbot, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|March 17, 2016
A randomized, placebo-controlled, double-blind phase IIb trial evaluating the safety and efficacy of tirasemtiv in patients with amyotrophic lateral sclerosisJeremy M Shefner, Andrew A Wolff, Lisa Meng, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|May 14, 2019
A phase III trial of tirasemtiv as a potential treatment for amyotrophic lateral sclerosisJeremy M Shefner, Merit E Cudkowicz, Orla Hardiman, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|July 12, 2022
Dying from ALS in Sweden: clinical status, setting, and symptomsStefan Sennfält, Ulf Kläppe, Sebastian Thams, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|July 19, 2022
A novel mutation in the ALS2 gene in an iranian kurdish family with juvenile amyotrophic lateral sclerosisYousef Daneshmandpour, Zahra Bahmanpour, Somayeh Kazeminasab, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|July 25, 2022
Analysis of STMN2 CA repeats in italian ALS patients shows no associationPaolo Niccolò Doronzio, Serena Lattante, Giuseppe Marangi, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|July 5, 2019
Implications of spirometric reference values for amyotrophic lateral sclerosisRuben P A van Eijk, Jaap N E Bakers, Michael A van Es, et al.Pageof 125