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Jong-Hee Chae

Showing results (11-20 of 272) with videos related to

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International Journal of Pediatric Otorhinolaryngology|January 17, 2020
Trajectory of change in the swallowing status in spinal muscular atrophy type IYoung-Ah Choi, Dong In Suh, Jong-Hee Chae, et al.
Brain & Development|March 24, 2006
Mutational analysis of TSC1 and TSC2 in Korean patients with tuberous sclerosis complexJi-Eun Choi, Jong-Hee Chae, Yong-Seung Hwang, et al.
Kidney International|May 15, 2017
The Case | An unusual case of recurrent hypokalemic periodic paralysisJong Hwan Jung, Jong Hee Chae, Ju Hung Song, et al.
Epilepsia|March 28, 2023
Outcomes of the second withdrawal of anti-seizure medication in patients with pediatric-onset epilepsyJaeso Cho, Hunmin Kim, Jong Hee Chae, et al.
Journal of Movement Disorders|July 17, 2019
Successful Pallidal Deep Brain Stimulation in a Patient with Childhood-Onset Generalized Dystonia with ANO3 MutationDallah Yoo, Han-Joon Kim, Jong-Hee Chae, et al.
European Journal of Medical Genetics|August 9, 2021
Extended phenotypes of PIEZO1-related lymphatic dysplasia caused by two novel compound heterozygous variantsSeungbok Lee, Soojin Park, Hwa Young Kim, et al.
Pediatric Neurology|December 12, 2022
Seizure Evolution and Outcome in Pediatric Autoimmune EncephalitisHyewon Woo, Youngkyu Shim, Jong-Hee Chae, et al.
Brain & Development|January 9, 2025
Analysis of initial seizure characteristics in patients with infantile onset genetic epilepsyYoungkyu Shim, Hunmin Kim, Jong Hee Chae, et al.
Pediatric Neurology|September 10, 2024
Exploring the Clinical Utility of Targeted MECP2 Testing in Real-World PracticeSoo Yeon Kim, Hyewon Woo, Byung Chan Lim, et al.
Journal of Child Neurology|November 6, 2004
Influence of MECP2 gene mutation and X-chromosome inactivation on the Rett syndrome phenotypeJong Hee Chae, Hee Hwang, Yong Seung Hwang, et al.
Pageof 28

Showing results (11-20 of 272) with videos related to

Sort By:
Pageof 28
International Journal of Pediatric Otorhinolaryngology|January 17, 2020
Trajectory of change in the swallowing status in spinal muscular atrophy type IYoung-Ah Choi, Dong In Suh, Jong-Hee Chae, et al.
Brain & Development|March 24, 2006
Mutational analysis of TSC1 and TSC2 in Korean patients with tuberous sclerosis complexJi-Eun Choi, Jong-Hee Chae, Yong-Seung Hwang, et al.
Kidney International|May 15, 2017
The Case | An unusual case of recurrent hypokalemic periodic paralysisJong Hwan Jung, Jong Hee Chae, Ju Hung Song, et al.
Epilepsia|March 28, 2023
Outcomes of the second withdrawal of anti-seizure medication in patients with pediatric-onset epilepsyJaeso Cho, Hunmin Kim, Jong Hee Chae, et al.
Journal of Movement Disorders|July 17, 2019
Successful Pallidal Deep Brain Stimulation in a Patient with Childhood-Onset Generalized Dystonia with ANO3 MutationDallah Yoo, Han-Joon Kim, Jong-Hee Chae, et al.
European Journal of Medical Genetics|August 9, 2021
Extended phenotypes of PIEZO1-related lymphatic dysplasia caused by two novel compound heterozygous variantsSeungbok Lee, Soojin Park, Hwa Young Kim, et al.
Pediatric Neurology|December 12, 2022
Seizure Evolution and Outcome in Pediatric Autoimmune EncephalitisHyewon Woo, Youngkyu Shim, Jong-Hee Chae, et al.
Brain & Development|January 9, 2025
Analysis of initial seizure characteristics in patients with infantile onset genetic epilepsyYoungkyu Shim, Hunmin Kim, Jong Hee Chae, et al.
Pediatric Neurology|September 10, 2024
Exploring the Clinical Utility of Targeted MECP2 Testing in Real-World PracticeSoo Yeon Kim, Hyewon Woo, Byung Chan Lim, et al.
Journal of Child Neurology|November 6, 2004
Influence of MECP2 gene mutation and X-chromosome inactivation on the Rett syndrome phenotypeJong Hee Chae, Hee Hwang, Yong Seung Hwang, et al.
Pageof 28