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Circulation|July 25, 2000
Deletion of a 5-cM region at chromosome 8p23 is associated with a spectrum of congenital heart defectsS Giglio, S L Graw, G Gimelli, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 13, 2018
Red Flags for early referral of people with symptoms suggestive of narcolepsy: a report from a national multidisciplinary panelL Vignatelli, E Antelmi, I Ceretelli, et al.Epilepsia|June 1, 2001
The costs of childhood epilepsy in Italy: comparative findings from three health care settingsR Guerrini, R Battini, A R Ferrari, et al.Clinical Genetics|April 23, 2016
A novel mutation in NDUFB11 unveils a new clinical phenotype associated with lactic acidosis and sideroblastic anemiaA Torraco, M Bianchi, D Verrigni, et al.Neurology|December 17, 2008
Periventricular heterotopia, mental retardation, and epilepsy associated with 5q14.3-q15 deletionC Cardoso, A Boys, E Parrini, et al.Epilepsia|December 28, 1999
No evidence of a major locus for benign familial infantile convulsions on chromosome 19q12-q13.1E Gennaro, M Malacarne, I Carbone, et al.Neurology|January 28, 2012
GLUT1 mutations are a rare cause of familial idiopathic generalized epilepsyP Striano, Y G Weber, M R Toliat, et al.Neurology|August 1, 1996
X-linked malformations of neuronal migrationW B Dobyns, E Andermann, F Andermann, et al.Epilepsia|March 1, 1997
Early-onset benign occipital seizure susceptibility syndromeC D Ferrie, A Beaumanoir, R Guerrini, et al.Human Mutation|January 22, 2008
Clinical and molecular features of mitochondrial DNA depletion due to mutations in deoxyguanosine kinaseD P Dimmock, Q Zhang, C Dionisi-Vici, et al.Pageof 33