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Journal of Neurology|June 3, 2000
Symptomatic treatment of respiratory and nutritional failure in amyotrophic lateral sclerosisO HardimanNeuromuscular Disorders : NMD|July 1, 1994
Dystrophin deficiency, altered cell signalling and fibre hypertrophyO HardimanHospital Medicine (London, England : 1998)|February 24, 2001
Pitfalls in the diagnosis of motor neurone diseaseO HardimanNeuroepidemiology|February 15, 2001
Environmental risk factors for amyotrophic lateral sclerosisC ArmonAmyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases|October 9, 2002
How can physicians and their patients with ALS decide to use the newly-available treatments to slow disease progression?C ArmonIrish Medical Journal|February 6, 2007
Detection rates of sexual dysfunction amongst patients with multiple sclerosis in an outpatient setting--can this be improved?S S O'Sullivan, O HardimanNeurology|December 1, 1996
Comparing composite scores based on maximal voluntary isometric contraction and on semiquantitative manual motor testing in measuring limb strength in patients with ALSC Armon, E PonrajJournal of the Neurological Sciences|December 16, 1998
Linear estimates of rates of disease progression as predictors of survival in patients with ALS entering clinical trialsC Armon, D MosesUndersea Biomedical Research|June 1, 1981
Interactions of thiopentone, light mineral oil, and pressure at frog sciatic nerveC Armon, D KeremJournal of Neurology, Neurosurgery, and Psychiatry|October 1, 1989
Electrophysiological signs of arteriovenous malformations of the spinal cordC Armon, J R DaubePageof 9