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Neurosurgical Review|September 18, 2009
Inherited cavernous malformations of the central nervous system: clinical and genetic features in 19 Swiss familiesC Graeni, F Stepper, M Sturzenegger, et al.Neuropediatrics|February 1, 1997
Genetic linkage analysis of a variant of juvenile onset neuronal ceroid lipofuscinosis with granular osmiophilic depositsA O'Rawe, H M Mitchison, R Williams, et al.The Review of Scientific Instruments|March 3, 2012
Development of electron beam ion source charge breeder for rare isotopes at Californium Rare Isotope Breeder UpgradeS Kondrashev, C Dickerson, A Levand, et al.Journal of Neurology, Neurosurgery, and Psychiatry|February 18, 2006
Patterns of hippocampal abnormalities in malformations of cortical developmentM A Montenegro, D Kinay, F Cendes, et al.Neurology|June 24, 2004
Posterior quadrantic dysplasia or hemi-hemimegalencephaly: a characteristic brain malformationM D D'Agostino, A Bastos, C Piras, et al.Clinical Genetics|September 18, 2012
Recurrent mutations in DNAJC5 cause autosomal dominant Kufs diseaseM Cadieux-Dion, E Andermann, P Lachance-Touchette, et al.Brain : a Journal of Neurology|June 4, 1999
Surgical outcome in patients with epilepsy and dual pathologyL M Li, F Cendes, F Andermann, et al.Neurology|May 25, 2005
Adult-onset epilepsy in focal cortical dysplasia of Taylor typeA M Siegel, G D Cascino, C E Elger, et al.American Journal of Human Genetics|December 1, 1999
Mapping of a gene determining familial partial epilepsy with variable foci to chromosome 22q11-q12L Xiong, M Labuda, D S Li, et al.Neurology|May 16, 2002
Resection of the lesion in patients with hypothalamic hamartomas and catastrophic epilepsyA Palmini, C Chandler, F Andermann, et al.Pageof 34