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Neuromuscular Disorders : NMD|February 8, 2011
Delayed presentation of invasive thymoma in myasthenia gravis: a case reportElizabeth C Galizia, Maria Elena Farrugia, Robert SwinglerMultiple Sclerosis (Houndmills, Basingstoke, England)|January 23, 2008
Chlamydia pneumoniae-specific serum immune complexes in patients with multiple sclerosisJohn Parratt, Roger Tavendale, Jonathan O'Riordan, et al.Journal of Neurology, Neurosurgery, and Psychiatry|July 24, 2015
Multidimensional apathy in ALS: validation of the Dimensional Apathy ScaleRatko Radakovic, Laura Stephenson, Shuna Colville, et al.The British Journal of General Practice : the Journal of the Royal College of General Practitioners|June 10, 2010
Primary care access to computed tomography for chronic headacheRalph Thomas, Alan Cook, Gavin Main, et al.Clinical and Translational Science|April 17, 2010
A patient suffering from hypokalemic periodic paralysis is deficient in skeletal muscle ATP-sensitive K channelsSofija Jovanović, Qingyou Du, Somnath Mukhopadhyay, et al.Cortex; a Journal Devoted to the Study of the Nervous System and Behavior|August 1, 2017
Multidimensional apathy and executive dysfunction in amyotrophic lateral sclerosisRatko Radakovic, Laura Stephenson, Judith Newton, et al.Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|November 20, 2009
Prognostic factors in ALS: A critical reviewAdriano Chiò, Giancarlo Logroscino, Orla Hardiman, et al.Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|May 4, 2010
Amyotrophic lateral sclerosis, physical exercise, trauma and sports: results of a population-based pilot case-control studyEttore Beghi, Giancarlo Logroscino, Adriano Chiò, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|May 14, 2015
Validation of the Edinburgh Cognitive and Behavioural Amyotrophic Lateral Sclerosis Screen (ECAS): A cognitive tool for motor disordersElaine Niven, Judith Newton, Jennifer Foley, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|March 6, 2019
Improved survival and 30-day mortality after gastrostomy in Scottish motor neurone disease patients: evidence from a national retrospective cohort study using STROBE criteriaGeorge H Gorrie, Siddharthan Chandran, Shuna Colville, et al.Pageof 3