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Dipole in Benign Rolandic Epilepsy. 2005

Mughis Sheerani, and Sajjad Ali, and Bhojo Khealani, and Ali Hassan, and Hina Punjwani
Department of Medicine, Section of Neurology, The Aga Khan University Hospital, Karachi. mughis.sheerani@aku.edu

UI MeSH Term Description Entries
D007223 Infant A child between 1 and 23 months of age. Infants
D011379 Prognosis A prediction of the probable outcome of a disease based on a individual's condition and the usual course of the disease as seen in similar situations. Prognostic Factor,Prognostic Factors,Factor, Prognostic,Factors, Prognostic,Prognoses
D002648 Child A person 6 to 12 years of age. An individual 2 to 5 years old is CHILD, PRESCHOOL. Children
D002675 Child, Preschool A child between the ages of 2 and 5. Children, Preschool,Preschool Child,Preschool Children
D004569 Electroencephalography Recording of electric currents developed in the brain by means of electrodes applied to the scalp, to the surface of the brain, or placed within the substance of the brain. EEG,Electroencephalogram,Electroencephalograms
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000293 Adolescent A person 13 to 18 years of age. Adolescence,Youth,Adolescents,Adolescents, Female,Adolescents, Male,Teenagers,Teens,Adolescent, Female,Adolescent, Male,Female Adolescent,Female Adolescents,Male Adolescent,Male Adolescents,Teen,Teenager,Youths
D000328 Adult A person having attained full growth or maturity. Adults are of 19 through 44 years of age. For a person between 19 and 24 years of age, YOUNG ADULT is available. Adults
D012189 Retrospective Studies Studies used to test etiologic hypotheses in which inferences about an exposure to putative causal factors are derived from data relating to characteristics of persons under study or to events or experiences in their past. The essential feature is that some of the persons under study have the disease or outcome of interest and their characteristics are compared with those of unaffected persons. Retrospective Study,Studies, Retrospective,Study, Retrospective
D019305 Epilepsy, Rolandic An autosomal dominant inherited partial epilepsy syndrome with onset between age 3 and 13 years. Seizures are characterized by PARESTHESIA and tonic or clonic activity of the lower face associated with drooling and DYSARTHRIA. In most cases, affected children are neurologically and developmentally normal. (From Epilepsia 1998 39;Suppl 4:S32-S41) Benign Childhood Epilepsy With Centro-Temporal Spikes,Benign Epilepsy With Centrotemporal Spikes,Benign Rolandic Epilepsy of Childhood,Epilepsy, Centrotemporal,Rolands Epilepsy,Sylvian Epilepsy,BCECTS,BECTS,Benign Epilepsy Of Childhood With Centrotemporal Spikes,Benign Rolandic Epilepsy,Centralopathic Epilepsy,Centrotemporal Epilepsy,Temporal-Central Focal Epilepsy,Benign Childhood Epilepsy With Centro Temporal Spikes,Centralopathic Epilepsies,Centrotemporal Epilepsies,Epilepsies, Centralopathic,Epilepsies, Centrotemporal,Epilepsies, Rolandic,Epilepsies, Temporal-Central Focal,Epilepsy, Benign Rolandic,Epilepsy, Centralopathic,Epilepsy, Rolands,Epilepsy, Sylvian,Epilepsy, Temporal-Central Focal,Focal Epilepsies, Temporal-Central,Focal Epilepsy, Temporal-Central,Rolandic Epilepsies,Rolandic Epilepsy,Rolandic Epilepsy, Benign,Temporal Central Focal Epilepsy,Temporal-Central Focal Epilepsies

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