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Muscle & Nerve|May 22, 2001
Severe infantile axonal neuropathy with respiratory failureJ M Wilmshurst, A Bye, C Rittey, et al.Journal of Neurology, Neurosurgery, and Psychiatry|August 1, 1993
Mitochondrial encephalomyopathy: variable clinical expression within a single kindredD Crimmins, J G Morris, G L Walker, et al.Acta Neuropathologica|January 1, 1992
Brain stem serotonin-synthesizing neurons in Alzheimer's disease: a clinicopathological correlationG M Halliday, H L McCann, R Pamphlett, et al.Journal of Clinical Pathology|April 29, 2005
Denaturing high performance liquid chromatography: high throughput mutation screening in familial hypertrophic cardiomyopathy and SNP genotyping in motor neurone diseaseB Yu, N A Sawyer, M Caramins, et al.Journal of Neurology, Neurosurgery, and Psychiatry|August 14, 1998
Neuroradiological features of six kindreds with MELAS tRNA(Leu) A2343G point mutation: implications for pathogenesisC M Sue, D S Crimmins, Y S Soo, et al.Acta Neuropathologica|June 19, 2002
Consensus neuropathological diagnosis of common dementia syndromes: testing and standardising the use of multiple diagnostic criteriaG Halliday, T Ng, M Rodriguez, et al.Neurology|March 27, 2009
A large-scale international meta-analysis of paraoxonase gene polymorphisms in sporadic ALSA-M Wills, S Cronin, A Slowik, et al.Pageof 6