Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Byung Chan Lim

Showing results (21-30 of 173) with videos related to

Pageof 18
Sort By:
Pediatric Research|September 11, 2024
Developmental screening of neurodevelopmental disorders before age 6: a nationwide health screening programJong Ho Cha, Soorack Ryu, Minjung Park, et al.
Frontiers in Neurology|August 8, 2022
Whole genomic approach in mutation discovery of infantile spasms patientsSeungbok Lee, Sesong Jang, Jong-Il Kim, et al.
Journal of Child Neurology|January 30, 2010
Ischemic stroke in a 7-month-old infant with antiphospholipid antibody and homozygous C677T methylenetetrahydrofolate reductase (MTHFR) polymorphismSe Hee Kim, Hee Hwang, Jong Hee Chae, et al.
Brain & Development|September 8, 2004
Clinical features of A3243G mitochondrial tRNA mutationJong Hee Chae, Hee Hwang, Byung Chan Lim, et al.
Journal of Clinical Medicine|December 8, 2020
Pediatric Miller Fisher Syndrome; Characteristic Presentation and Comparison with Adult Miller Fisher SyndromeYeonji Jang, Jae-Hwan Choi, Jong Hee Chae, et al.
Epilepsy Research|August 7, 2013
Low incidence of SCN1A genetic mutation in patients with hemiconvulsion-hemiplegia-epilepsy syndromeDong Wook Kim, Byung Chan Lim, Ki Joong Kim, et al.
Journal of the Neurological Sciences|March 16, 2010
A single large-scale deletion of mtDNA in a child with recurrent encephalopathy and tubulopathyJong-Hee Chae, Byung Chan Lim, Hae Il Cheong, et al.
Brain & Development|March 1, 2023
A case of pediatric anti-leucine-rich glioma inactivated 1 encephalitis with faciobrachial dystonic seizureSeoyun Jang, Soo Yeon Kim, Woo Joong Kim, et al.
Molecular Genetics & Genomic Medicine|August 24, 2021
Genetic and clinical heterogeneity in Korean patients with Rubinstein-Taybi syndromeNaye Choi, Hwa Young Kim, Byung Chan Lim, et al.
Encephalitis (Seoul, Korea)|July 20, 2023
Angiography-negative childhood primary angiitis of the central nervous system diagnosed by open brain biopsy: a case reportDayun Kang, Soo Yeon Kim, Jong Hee Chae, et al.
Pageof 18

Showing results (21-30 of 173) with videos related to

Sort By:
Pageof 18
Pediatric Research|September 11, 2024
Developmental screening of neurodevelopmental disorders before age 6: a nationwide health screening programJong Ho Cha, Soorack Ryu, Minjung Park, et al.
Frontiers in Neurology|August 8, 2022
Whole genomic approach in mutation discovery of infantile spasms patientsSeungbok Lee, Sesong Jang, Jong-Il Kim, et al.
Journal of Child Neurology|January 30, 2010
Ischemic stroke in a 7-month-old infant with antiphospholipid antibody and homozygous C677T methylenetetrahydrofolate reductase (MTHFR) polymorphismSe Hee Kim, Hee Hwang, Jong Hee Chae, et al.
Brain & Development|September 8, 2004
Clinical features of A3243G mitochondrial tRNA mutationJong Hee Chae, Hee Hwang, Byung Chan Lim, et al.
Journal of Clinical Medicine|December 8, 2020
Pediatric Miller Fisher Syndrome; Characteristic Presentation and Comparison with Adult Miller Fisher SyndromeYeonji Jang, Jae-Hwan Choi, Jong Hee Chae, et al.
Epilepsy Research|August 7, 2013
Low incidence of SCN1A genetic mutation in patients with hemiconvulsion-hemiplegia-epilepsy syndromeDong Wook Kim, Byung Chan Lim, Ki Joong Kim, et al.
Journal of the Neurological Sciences|March 16, 2010
A single large-scale deletion of mtDNA in a child with recurrent encephalopathy and tubulopathyJong-Hee Chae, Byung Chan Lim, Hae Il Cheong, et al.
Brain & Development|March 1, 2023
A case of pediatric anti-leucine-rich glioma inactivated 1 encephalitis with faciobrachial dystonic seizureSeoyun Jang, Soo Yeon Kim, Woo Joong Kim, et al.
Molecular Genetics & Genomic Medicine|August 24, 2021
Genetic and clinical heterogeneity in Korean patients with Rubinstein-Taybi syndromeNaye Choi, Hwa Young Kim, Byung Chan Lim, et al.
Encephalitis (Seoul, Korea)|July 20, 2023
Angiography-negative childhood primary angiitis of the central nervous system diagnosed by open brain biopsy: a case reportDayun Kang, Soo Yeon Kim, Jong Hee Chae, et al.
Pageof 18