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European Journal of Neurology|February 14, 2018
Novel mutations in DNAJB6 cause LGMD1D and distal myopathy in French familiesP H Jonson, J Palmio, M Johari, et al.Journal of Neurology|March 3, 2009
Wernicke encephalopathy and Creutzfeldt-Jakob diseaseA Bertrand, J P Brandel, Y Grignon, et al.American Journal of Human Genetics|January 1, 1996
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, genetic homogeneity, and mapping of the locus within a 2-cM intervalA Ducros, T Nagy, S Alamowitch, et al.Neuro-Chirurgie|April 21, 2007
[Intracranial ependymomas in adult patients. Diagnosis and histological prognostic factors]D Figarella-Branger, P Metellus, M Barrié, et al.Pageof 15