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American Journal of Medical Genetics|October 2, 2001
Epilepsy and genetic malformations of the cerebral cortexR Guerrini, R CarrozzoSeizure|December 26, 2001
Epileptogenic brain malformations: clinical presentation, malformative patterns and indications for genetic testingR Guerrini, R CarrozzoBrain & Development|April 17, 1998
Paroxysmal tonic upgaze of childhood with ataxia: a benign transient dystonia with autosomal dominant inheritanceR Guerrini, A Belmonte, R CarrozzoNeurology|June 17, 1999
Bilateral perisylvian polymicrogyria in three generationsR Borgatti, F Triulzi, C Zucca, et al.Neurology|March 27, 2002
Familial periventricular heterotopia: missense and distal truncating mutations of the FLN1 geneF Moro, R Carrozzo, P Veggiotti, et al.Annals of Neurology|January 13, 2000
A nonsense mutation of the ATRX gene causing mild mental retardation and epilepsyR Guerrini, J L Shanahan, R Carrozzo, et al.Annals of Neurology|March 11, 1999
Autosomal recessive rolandic epilepsy with paroxysmal exercise-induced dystonia and writer's cramp: delineation of the syndrome and gene mapping to chromosome 16p12-11.2R Guerrini, P Bonanni, N Nardocci, et al.Brain : a Journal of Neurology|November 10, 2001
Autosomal dominant cortical myoclonus and epilepsy (ADCME) with complex partial and generalized seizures: A newly recognized epilepsy syndrome with linkage to chromosome 2p11.1-q12.2R Guerrini, P Bonanni, A Patrignani, et al.Journal of Bioenergetics and Biomembranes|April 1, 1997
Disorders of nuclear-mitochondrial intergenomic signallingM Zeviani, V Petruzzella, R CarrozzoPageof 33