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Jong-Hee Chae

Showing results (41-50 of 272) with videos related to

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Neurosurgery|October 1, 2010
Papillary glioneuronal tumor present in a patient with encephalocraniocutaneous lipomatosis: case reportJi Hoon Phi, Sung-Hye Park, Jong Hee Chae, et al.
Neuromuscular Disorders : NMD|August 29, 2021
Infant with early onset bilateral facial and bulbar weakness: Successful treatment of riboflavin in multiple acyl-CoA dehydrogenase deficiency caused by biallelic nonsense FLAD1 variantsYun Jeong Lee, Soo Yeon Kim, Man Jin Kim, et al.
Brain & Development|November 29, 2020
A case of CHOPS syndrome accompanied with moyamoya disease and systemic vasculopathySoo Yeon Kim, Man Jin Kim, Su Jin Kim, 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.
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.
Pediatric Research|April 7, 2007
A novel ND3 mitochondrial DNA mutation in three Korean children with basal ganglia lesions and complex I deficiencyJong Hee Chae, Jin Sook Lee, Ki Joong Kim, 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.
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.
Pageof 28

Showing results (41-50 of 272) with videos related to

Sort By:
Pageof 28
Neurosurgery|October 1, 2010
Papillary glioneuronal tumor present in a patient with encephalocraniocutaneous lipomatosis: case reportJi Hoon Phi, Sung-Hye Park, Jong Hee Chae, et al.
Neuromuscular Disorders : NMD|August 29, 2021
Infant with early onset bilateral facial and bulbar weakness: Successful treatment of riboflavin in multiple acyl-CoA dehydrogenase deficiency caused by biallelic nonsense FLAD1 variantsYun Jeong Lee, Soo Yeon Kim, Man Jin Kim, et al.
Brain & Development|November 29, 2020
A case of CHOPS syndrome accompanied with moyamoya disease and systemic vasculopathySoo Yeon Kim, Man Jin Kim, Su Jin Kim, 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.
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.
Pediatric Research|April 7, 2007
A novel ND3 mitochondrial DNA mutation in three Korean children with basal ganglia lesions and complex I deficiencyJong Hee Chae, Jin Sook Lee, Ki Joong Kim, 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.
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.
Pageof 28