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BMJ Case Reports|June 21, 2011
Vacuolar leucoencephalopathy and pulvinar sign in association with coeliac diseaseA M Ryan, J Ryan, M Wan-Ahmed, et al.Neurology|September 1, 1996
Reversible parkinsonism and cognitive impairment with chronic valproate useC Armon, C Shin, P Miller, et al.Neurology|November 24, 2004
A novel candidate region for ALS on chromosome 14q11.2M J Greenway, M D Alexander, S Ennis, et al.BMC Medical Education|August 29, 2022
Psychological safety between pediatric residents and nurses and the impact of an interdisciplinary simulation curriculumCourtney Haviland, Janet Green, Kristina Dzara, et al.Journal of Neurology, Neurosurgery, and Psychiatry|December 15, 2007
Descriptive epidemiology of amyotrophic lateral sclerosis: new evidence and unsolved issuesG Logroscino, B J Traynor, O Hardiman, et al.Progress in Neurobiology|September 14, 2011
On the development of markers for pathological TDP-43 in amyotrophic lateral sclerosis with and without dementiaF Geser, D Prvulovic, L O'Dwyer, et al.Neurology|August 24, 2005
Evidence of reduced frequency of spinal muscular atrophy type I in the Cuban populationT Zaldívar, Y Montejo, A M Acevedo, et al.Neurology|May 1, 1996
Relationship of the Tufts Quantitative Neuromuscular Exam (TQNE) and the Sickness Impact Profile (SIP) in measuring progression of ALS. SSNJV/CNTF ALS Study GroupD McGuire, L Garrison, C Armon, et al.Muscle & Nerve|June 8, 2000
Linear estimates of disease progression predict survival in patients with amyotrophic lateral sclerosisC Armon, M C Graves, D Moses, et al.European Journal of Neurology|December 6, 2005
EFNS task force on management of amyotrophic lateral sclerosis: guidelines for diagnosing and clinical care of patients and relativesP M Andersen, G D Borasio, R Dengler, et al.Pageof 9