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Epilepsia|January 1, 1993
Progressive myoclonus epilepsies: clinical and genetic aspectsS F Berkovic, J Cochius, E Andermann, et al.
Neurology|June 1, 1987
Concepts of absence epilepsies: discrete syndromes or biological continuum?S F Berkovic, F Andermann, E Andermann, et al.
Human Mutation|January 1, 1997
Mutations and polymorphisms in the tuberous sclerosis complex gene on chromosome 16K S Au, J A Rodriguez, E Rodriguez, et al.
American Journal of Medical Genetics|May 3, 1996
Diffuse polymicrogyria associated with an unusual pattern of multiple congenital anomalies including turribrachycephaly and hypogenitalismR D Cohn, G Gillessen-Kaesbach, W B Dobyns, et al.
Human Genetics|April 1, 1992
The French Canadian Tay-Sachs disease deletion mutation: identification of probable foundersM De Braekeleer, P Hechtman, E Andermann, et al.
Journal of Neurophysiology|December 1, 1990
Epileptiform activity induced by low chloride medium in the CA1 subfield of the hippocampal sliceM Avoli, C Drapeau, P Perreault, et al.
Experimental Brain Research|January 1, 1991
Bicuculline-induced epileptogenesis in the human neocortex maintained in vitroG G Hwa, M Avoli, A Oliver, et al.
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