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Byung Chan Lim

Showing results (31-40 of 173) with videos related to

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Journal of Child Neurology|April 8, 2011
De novo interstitial deletion of 3q22.3-q25.2 encompassing FOXL2, ATR, ZIC1, and ZIC4 in a patient with blepharophimosis/ptosis/epicanthus inversus syndrome, Dandy-Walker malformation, and global developmental delayByung Chan Lim, Woong Yang Park, Eul-Ju Seo, et al.
Chonnam Medical Journal|May 10, 2012
Outcome evaluation of intravenous infusion of urokinase for acute ischemic strokeRae Seop Lee, Young Chul Ok, Jun Seob Lim, et al.
American Journal of Medical Genetics. Part A|May 28, 2016
GM3 synthase deficiency due to ST3GAL5 variants in two Korean female siblings: Masquerading as Rett syndrome-like phenotypeJin Sook Lee, Yongjin Yoo, Byung Chan Lim, et al.
Journal of Cerebrovascular and Endovascular Neurosurgery|April 26, 2014
Clipping of incidental aneurysm of middle cerebral artery through small temporal craniotomy and linear skin incisionJong Hyun Mun, Kyu Yong Cho, Rae Seop Lee, et al.
Brain & Development|June 23, 2016
Averaged EEG spike dipole analysis may predict atypical outcome in Benign Childhood Epilepsy with Centrotemporal Spikes (BCECTS)Hunmin Kim, Il Han Yoo, Byung Chan Lim, et al.
Child Neurology Open|May 16, 2017
<i>FOXG1</i> Mutation is a Low-Incidence Genetic Cause in Atypical Rett SyndromeChristine K Byun, Jin Sook Lee, Byung Chan Lim, et al.
Journal of Medical Genetics|January 31, 2015
Utility of next generation sequencing in genetic diagnosis of early onset neuromuscular disordersJong Hee Chae, Valeria Vasta, Anna Cho, et al.
Epilepsy & Behavior : E&B|June 28, 2025
Switching from oxcarbazepine to eslicarbazepine in pediatric patients with focal epilepsy is safe and well-toleratedYoungkyu Shim, Woo Joong Kim, Hunmin Kim, et al.
Gene|May 5, 2015
Alpha-thalassemia X-linked intellectual disability syndrome identified by whole exome sequencing in two boys with white matter changes and developmental retardationJin Sook Lee, Sangmoon Lee, Byung Chan Lim, et al.
Epilepsy & Behavior : E&B|May 15, 2012
Paroxysmal nonepileptic events in pediatric patients confirmed by long-term video-EEG monitoring--Single tertiary center review of 143 patientsSeung Hyo Kim, Hunmin Kim, Byung Chan Lim, et al.
Pageof 18

Showing results (31-40 of 173) with videos related to

Sort By:
Pageof 18
Journal of Child Neurology|April 8, 2011
De novo interstitial deletion of 3q22.3-q25.2 encompassing FOXL2, ATR, ZIC1, and ZIC4 in a patient with blepharophimosis/ptosis/epicanthus inversus syndrome, Dandy-Walker malformation, and global developmental delayByung Chan Lim, Woong Yang Park, Eul-Ju Seo, et al.
Chonnam Medical Journal|May 10, 2012
Outcome evaluation of intravenous infusion of urokinase for acute ischemic strokeRae Seop Lee, Young Chul Ok, Jun Seob Lim, et al.
American Journal of Medical Genetics. Part A|May 28, 2016
GM3 synthase deficiency due to ST3GAL5 variants in two Korean female siblings: Masquerading as Rett syndrome-like phenotypeJin Sook Lee, Yongjin Yoo, Byung Chan Lim, et al.
Journal of Cerebrovascular and Endovascular Neurosurgery|April 26, 2014
Clipping of incidental aneurysm of middle cerebral artery through small temporal craniotomy and linear skin incisionJong Hyun Mun, Kyu Yong Cho, Rae Seop Lee, et al.
Brain & Development|June 23, 2016
Averaged EEG spike dipole analysis may predict atypical outcome in Benign Childhood Epilepsy with Centrotemporal Spikes (BCECTS)Hunmin Kim, Il Han Yoo, Byung Chan Lim, et al.
Child Neurology Open|May 16, 2017
<i>FOXG1</i> Mutation is a Low-Incidence Genetic Cause in Atypical Rett SyndromeChristine K Byun, Jin Sook Lee, Byung Chan Lim, et al.
Journal of Medical Genetics|January 31, 2015
Utility of next generation sequencing in genetic diagnosis of early onset neuromuscular disordersJong Hee Chae, Valeria Vasta, Anna Cho, et al.
Epilepsy & Behavior : E&B|June 28, 2025
Switching from oxcarbazepine to eslicarbazepine in pediatric patients with focal epilepsy is safe and well-toleratedYoungkyu Shim, Woo Joong Kim, Hunmin Kim, et al.
Gene|May 5, 2015
Alpha-thalassemia X-linked intellectual disability syndrome identified by whole exome sequencing in two boys with white matter changes and developmental retardationJin Sook Lee, Sangmoon Lee, Byung Chan Lim, et al.
Epilepsy & Behavior : E&B|May 15, 2012
Paroxysmal nonepileptic events in pediatric patients confirmed by long-term video-EEG monitoring--Single tertiary center review of 143 patientsSeung Hyo Kim, Hunmin Kim, Byung Chan Lim, et al.
Pageof 18