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Journal of Neurovirology|April 30, 2008
Cortical maldevelopment in congenital cytomegalovirus infection transmitted by a woman with preexisting immunityC Arpino, G Castelli Gattinara, M Rosso, et al.Neuropediatrics|April 1, 1993
Familial white matter hypoplasia, agenesis of the corpus callosum, mental retardation and growth deficiency: a new distinctive syndromeP Curatolo, M R Cilio, E Del Giudice, et al.Archives of Gynecology and Obstetrics|March 4, 2023
"Time is on my side". Disease trajectory of vulvodynia: a systematic review with a narrative synthesisG E Cetera, C E M Merli, F Facchin, et al.Journal of Neurology, Neurosurgery, and Psychiatry|April 18, 2003
GABA(A) receptor active steroids are altered in epilepsy patients with tuberous sclerosisF di Michele, M Verdecchia, M Dorofeeva, et al.Neuropediatrics|July 2, 2009
Genetic polymorphism and idiopathic generalized epilepsy. Evidence of interaction between haptoglobin and ACP1 systemsF Gloria-Bottini, P Lucarelli, P Saccucci, et al.Journal of Child Neurology|February 26, 1998
Frontal lobe epilepsy associated with tuberous sclerosis: electroencephalographic-magnetic resonance image fusioningS Seri, A Cerquiglini, F Pisani, et al.Journal of Child Neurology|November 26, 1999
Seizures in Chiari I malformation: a clinical and electroencephalographic studyM Elia, R Biondi, V Sofia, et al.Journal of Child Neurology|September 29, 2001
Prenatal and perinatal determinants of neonatal seizures occurring in the first week of lifeC Arpino, S Domizio, M P Carrieri, et al.European Journal of Neurology|September 22, 2006
Oxcarbazepine and atypical evolution of benign idiopathic focal epilepsy of childhoodS Grosso, M Balestri, R M Di Bartolo, et al.Neurogenetics|October 19, 2004
Convulsive disorder and genetic polymorphism. Association of idiopathic generalized epilepsy with haptoglobin polymorphismP Saccucci, M Verdecchia, A Piciullo, et al.Pageof 8