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International Journal of Geriatric Psychiatry|January 30, 2020
Identifying delirium in Parkinson disease: A pilot studyRachael A Lawson, Sarah J Richardson, Alison J Yarnall, et al.Journal of Medical Genetics|June 4, 1998
The North Cumbria Community Genetics ProjectD S Chase, E J Tawn, L Parker, et al.Blood|October 5, 2007
Membrane cofactor protein mutations in atypical hemolytic uremic syndrome (aHUS), fatal Stx-HUS, C3 glomerulonephritis, and the HELLP syndromeCelia J Fang, Veronique Fremeaux-Bacchi, M Kathryn Liszewski, et al.Human Genetics|March 1, 1987
Prenatal diagnosis of X-linked choroideremia with mental retardation, associated with a cytologically detectable X-chromosome deletionS V Hodgson, M E Robertson, C N Fear, et al.Practical Neurology|March 10, 2011
An unusual gait following the discovery of a new diseaseM J Keogh, A Khan, G Gorman, et al.Movement Disorders : Official Journal of the Movement Disorder Society|May 31, 2007
Basal ganglia cholinergic and dopaminergic function in progressive supranuclear palsyNaomi M Warren, Margaret A Piggott, Elizabeth Greally, et al.Nature|October 15, 1987
Preferential deletion of exons in Duchenne and Becker muscular dystrophiesS M Forrest, G S Cross, A Speer, et al.Brain : a Journal of Neurology|August 15, 2019
Fluctuating cognition in the Lewy body dementiasSeán O'Dowd, Julia Schumacher, David J Burn, et al.British Heart Journal|November 1, 1987
Conjoined twins, right atrial isomerism, and sequential segmental analysisM B Rossi, J Burn, S Y Ho, et al.Neurobiology of Aging|July 29, 2011
No evidence of substantia nigra telomere shortening in Parkinson's diseaseGavin Hudson, David Faini, Andrea Stutt, et al.Pageof 58