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Human Genetics|September 1, 1986
The myoblast defect identified in Duchenne muscular dystrophy is not a primary expression of the DMD mutation. Clonal analysis of myoblasts from five double heterozygotes for two X-linked loci: DMD and G6PDC Webster, G Filippi, A Rinaldi, et al.Brain Research|February 25, 1977
Longitudinal changes of brain amino acid content occurring before, during and after epileptic activityR Mutani, L Durelli, M Mazzarino, et al.European Neurology|January 1, 1988
Free drug levels monitoring as a detector of false metabolic refractory epilepsyM Gianelli, S Gentile, L Verzè, et al.Italian Journal of Neurological Sciences|April 1, 1994
Plasma amino acid alterations in idiopathic generalized epilepsy: an investigation in probands and their first-degree relativesF Monaco, M Gianelli, M P Schiavella, et al.Functional Neurology|October 1, 1986
Neurophysiological mechanisms underlying epileptogenesisR MutaniClinical Neuropharmacology|March 1, 1983
The current status of taurine in epilepsyL Durelli, R MutaniEpilepsia|October 1, 1980
Mechanisms of interaction of asymmetrical bilateral epileptogenic foci in neocortexR Mutani, L DurelliJournal of the Neurological Sciences|June 1, 1979
Myotonia, potassium and taurine. A preliminary reportL Durelli, R MutaniJournal of Neurology, Neurosurgery, and Psychiatry|October 25, 2002
Chronic alcohol use and first symptomatic epileptic seizuresM Leone, C Tonini, G Bogliun, et al.Acta Neurologica Scandinavica|July 1, 1990
Conventional vs controlled-release carbamazepine: a multicentre, double-blind, cross-over studyR Canger, A C Altamura, O Belvedere, et al.Pageof 34