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Byung Chan Lim

Showing results (81-90 of 173) with videos related to

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Epilepsy Research|March 31, 2012
Coexisting seizures in patients with infantile spasms confirmed by long-term video-electroencephalography monitoringHunmin Kim, Jeong Ho Lee, Hye Won Ryu, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|February 13, 2013
Distinct neurological features in a patient with Schinzel-Giedion syndrome caused by a recurrent SETBP1 mutationJung Min Ko, Byung Chan Lim, Ki Joong Kim, et al.
Brain & Development|July 3, 2017
Severe hypotonia and postnatal growth impairment in a girl with a missense mutation in COL1A1: Implication of expanded phenotypic spectrum of type I collagenopathyJin Sook Lee, Jieun Seo, Anna Cho, et al.
Brain & Development|July 28, 2020
Novel compound heterozygous ACO2 mutations in an infant with progressive encephalopathy: A newly identified neurometabolic syndromeJi Soo Park, Man Jin Kim, Soo Yeon Kim, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|December 19, 2014
Rare coincidence of familial central core disease and hemophagocytic lymphohistiocytosisJin Sook Lee, Byung Chan Lim, Ki Joong Kim, et al.
Journal of Korean Medical Science|June 13, 2012
Magnetoencephalography in pediatric lesional epilepsy surgeryHunmin Kim, Byung Chan Lim, Woorim Jeong, et al.
Epilepsy Research|December 20, 2014
Epilepsy phenotype associated with a chromosome 2q24.3 deletion involving SCN1A: Migrating partial seizures of infancy or atypical Dravet syndrome?Byung Chan Lim, Hee Hwang, Hunmin Kim, et al.
Pediatric Neurology|December 2, 2023
Role of Perampanel in the Management of Pediatric Epilepsies in Asia: Expert OpinionWang-Tso Lee, Derrick Wei Shih Chan, Sheffali Gulati, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|March 28, 2013
Short-term efficacy and tolerability of rufinamide adjunctive therapy in children with refractory generalised epilepsySe Hee Kim, Jeong Ho Lee, Hye Won Ryu, et al.
Annals of Clinical and Laboratory Science|August 26, 2018
Neuropathy, Ataxia, Retinitis Pigmentosa-like Phenotype Associated with a Mitochondrial <i>G8363A</i> Mutation in a FamilySooYeon Kim, JiYoon Han, Hyun Ah Kim, et al.
Pageof 18

Showing results (81-90 of 173) with videos related to

Sort By:
Pageof 18
Epilepsy Research|March 31, 2012
Coexisting seizures in patients with infantile spasms confirmed by long-term video-electroencephalography monitoringHunmin Kim, Jeong Ho Lee, Hye Won Ryu, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|February 13, 2013
Distinct neurological features in a patient with Schinzel-Giedion syndrome caused by a recurrent SETBP1 mutationJung Min Ko, Byung Chan Lim, Ki Joong Kim, et al.
Brain & Development|July 3, 2017
Severe hypotonia and postnatal growth impairment in a girl with a missense mutation in COL1A1: Implication of expanded phenotypic spectrum of type I collagenopathyJin Sook Lee, Jieun Seo, Anna Cho, et al.
Brain & Development|July 28, 2020
Novel compound heterozygous ACO2 mutations in an infant with progressive encephalopathy: A newly identified neurometabolic syndromeJi Soo Park, Man Jin Kim, Soo Yeon Kim, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|December 19, 2014
Rare coincidence of familial central core disease and hemophagocytic lymphohistiocytosisJin Sook Lee, Byung Chan Lim, Ki Joong Kim, et al.
Journal of Korean Medical Science|June 13, 2012
Magnetoencephalography in pediatric lesional epilepsy surgeryHunmin Kim, Byung Chan Lim, Woorim Jeong, et al.
Epilepsy Research|December 20, 2014
Epilepsy phenotype associated with a chromosome 2q24.3 deletion involving SCN1A: Migrating partial seizures of infancy or atypical Dravet syndrome?Byung Chan Lim, Hee Hwang, Hunmin Kim, et al.
Pediatric Neurology|December 2, 2023
Role of Perampanel in the Management of Pediatric Epilepsies in Asia: Expert OpinionWang-Tso Lee, Derrick Wei Shih Chan, Sheffali Gulati, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|March 28, 2013
Short-term efficacy and tolerability of rufinamide adjunctive therapy in children with refractory generalised epilepsySe Hee Kim, Jeong Ho Lee, Hye Won Ryu, et al.
Annals of Clinical and Laboratory Science|August 26, 2018
Neuropathy, Ataxia, Retinitis Pigmentosa-like Phenotype Associated with a Mitochondrial <i>G8363A</i> Mutation in a FamilySooYeon Kim, JiYoon Han, Hyun Ah Kim, et al.
Pageof 18