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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 : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|January 5, 2012
Non-invasive ventilation and gastrostomy may not impact overall quality of life in patients with ALSKristen Zamietra, Erik B Lehman, Stephanie H Felgoise, et al.Muscle & Nerve|July 2, 2013
H63D HFE polymorphisms are associated with increased disease duration and decreased muscle superoxide dismutase-1 expression in amyotrophic lateral sclerosis patientsXiaowei W Su, Sang Y Lee, Ryan M Mitchell, et al.Muscle & Nerve|July 21, 2018
Amyotrophic lateral sclerosis-specific quality of life-short form (ALSSQOL-SF): A brief, reliable, and valid version of the ALSSQOL-RStephanie H Felgoise, Richard Feinberg, Helen E Stephens, et al.Muscle & Nerve|January 26, 2017
Fixed dynamometry is more sensitive than vital capacity or ALS rating scalePatricia L Andres, Margaret Peggy Allred, Helen E Stephens, et al.Pageof 2