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Journal of Child Neurology, ISSN 0883-0738, 05/2009, Volume 24, Issue 5, pp. 544 - 550
We describe 3 patients with bilateral operculum syndrome. They presented with various degrees of suprabulbar (pseudobulbar) signs in addition to delay in... 
Benign childhood epilepsy with centrotemporal (Rolandic) spikes | Schizencephaly | Perisylvian polymicrogyria | Suprabulbar (pseudobulbar) paresis | Developmental language disorder | Operculum | Opercular underdevelopment | schizencephaly | CEREBRAL OPERCULUM | ROLANDIC EPILEPSY | ABNORMALITIES | benign childhood epilepsy with centrotemporal (Rolandic) spikes | DISORDERS | SPEECH | CLINICAL NEUROLOGY | perisylvian polymicrogyria | CHILDREN | suprabulbar (pseudobulbar) paresis | operculum | opercular underdevelopment | developmental language disorder | INFANTS | WORSTER-DROUGHT-SYNDROME | PEDIATRICS | Humans | Cerebral Palsy - physiopathology | Movement Disorders - diagnosis | Male | Electroencephalography | Epilepsy - physiopathology | Speech Disorders - pathology | Developmental Disabilities - pathology | Cerebral Palsy - diagnosis | Female | Temporal Lobe - pathology | Child | Developmental Disabilities - diagnosis | Speech Disorders - diagnosis | Developmental Disabilities - physiopathology | Cognition Disorders - physiopathology | Diagnosis, Differential | Cerebral Palsy - pathology | Movement Disorders - pathology | Brain - physiopathology | Frontal Lobe - physiopathology | Cognition Disorders - pathology | Paresis - pathology | Speech Disorders - physiopathology | Syndrome | Epilepsy - diagnosis | Neuropsychological Tests | Cognition Disorders - diagnosis | Magnetic Resonance Imaging | Temporal Lobe - physiopathology | Movement Disorders - physiopathology | Brain - pathology | Epilepsy - pathology | Frontal Lobe - pathology | Paresis - diagnosis | Paresis - physiopathology
Journal Article
Journal Article
Journal of Child Neurology, ISSN 0883-0738, 04/2009, Volume 24, Issue 4, pp. 421 - 424
Schizencephaly is an uncommon congenital malformation of neuronal migration characterized by a gray matter—lined cleft extending from the pial surface to the... 
Thrombophilia | Schizencephaly | Methyltetrahydrofolate reductase | schizencephaly | POLYMICROGYRIA | HOMEOBOX GENE EMX2 | V-LEIDEN MUTATION | CYTOMEGALOVIRUS-INFECTION | CLINICAL NEUROLOGY | FEATURES | TWIN | thrombophilia | MALFORMATIONS | GERMLINE MUTATIONS | PEDIATRICS | methyltetrahydrofolate reductase | ABSENCE | Developmental Disabilities - metabolism | Humans | Gene Expression Regulation, Developmental - genetics | Cognition Disorders - metabolism | Infant | Developmental Disabilities - genetics | Cell Movement - genetics | Cerebrum - abnormalities | Methylenetetrahydrofolate Reductase (NADPH2) - genetics | DNA Mutational Analysis | Malformations of Cortical Development - physiopathology | Female | Cerebrum - physiopathology | Thrombophilia - genetics | Developmental Disabilities - physiopathology | Cognition Disorders - physiopathology | Genetic Predisposition to Disease - genetics | Thrombophilia - physiopathology | Malformations of Cortical Development - metabolism | Genotype | Cognition Disorders - genetics | Malformations of Cortical Development - genetics | Mutation - genetics | Magnetic Resonance Imaging | Movement Disorders - metabolism | Movement Disorders - physiopathology | Organogenesis - genetics | Genetic Markers - genetics | Factor V - genetics | Movement Disorders - genetics | Thrombophilia - metabolism
Journal Article
Journal Article
Journal Article
Journal Article