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

Sun Ah Choi

Showing results (41-50 of 63) with videos related to

Pageof 7
Sort By:
American Journal of Medical Genetics. Part A|July 14, 2016
Atypical presentation of infantile-onset farber disease with novel ASAH1 mutationsSoo Yeon Kim, Sun Ah Choi, Sangmoon Lee, et al.
Brain & Development|December 10, 2019
Change of centrotemporal spikes from onset to remission in self-limited epilepsy with centrotemporal spikes (SLECTS)Ji Yeon Han, Sun Ah Choi, Yoon Gi Chung, et al.
Muscle & Nerve|February 7, 2018
Collagen VI-related myopathy: Expanding the clinical and genetic spectrumSoo Yeon Kim, Woo Joong Kim, Hyuna Kim, et al.
Clinical and Experimental Pediatrics|February 19, 2026
Long-term outcome in children with infantile epileptic spasms syndrome: a multicenter retrospective study in KoreaSun Ah Choi, Minhye Kim, Hye Jin Kim, et al.
Journal of Epilepsy Research|January 28, 2015
Screening Autoimmune Anti-neuronal Antibodies in Pediatric Patients with Suspected Autoimmune EncephalitisSoo Yeon Kim, Sun Ah Choi, Hye Won Ryu, et al.
Journal of Movement Disorders|May 29, 2014
A case of isolated middle cerebral artery stenosis with hemichorea and moyamoya pattern collateralizationSeok Jong Chung, Hyung Seok Lee, Han Soo Yoo, et al.
Brain & Development|April 20, 2021
Early-onset autosomal dominant GTP-cyclohydrolase I deficiency: Diagnostic delay and residual motor signsWooJoong Kim, Jae So Cho, Young Kyu Shim, et al.
Annals of Laboratory Medicine|August 26, 2017
A Unique Mutational Spectrum of MLC1 in Korean Patients With Megalencephalic Leukoencephalopathy With Subcortical Cysts: p.Ala275Asp Founder Mutation and Maternal Uniparental Disomy of Chromosome 22Sun Ah Choi, Soo Yeon Kim, Jihoo Yoon, et al.
Epilepsy Research|December 4, 2017
Surgical outcome and predictive factors of epilepsy surgery in pediatric isolated focal cortical dysplasiaSun Ah Choi, Soo Yeon Kim, Hyuna Kim, et al.
Journal of Clinical Neurology (Seoul, Korea)|July 14, 2020
Clinical Spectrum of Myelin Oligodendrocyte Glycoprotein-Immunoglobulin G-Associated Disease in Korean ChildrenIl Han Yoo, WooJoong Kim, Youngkyu Shim, et al.
Pageof 7

Showing results (41-50 of 63) with videos related to

Sort By:
Pageof 7
American Journal of Medical Genetics. Part A|July 14, 2016
Atypical presentation of infantile-onset farber disease with novel ASAH1 mutationsSoo Yeon Kim, Sun Ah Choi, Sangmoon Lee, et al.
Brain & Development|December 10, 2019
Change of centrotemporal spikes from onset to remission in self-limited epilepsy with centrotemporal spikes (SLECTS)Ji Yeon Han, Sun Ah Choi, Yoon Gi Chung, et al.
Muscle & Nerve|February 7, 2018
Collagen VI-related myopathy: Expanding the clinical and genetic spectrumSoo Yeon Kim, Woo Joong Kim, Hyuna Kim, et al.
Clinical and Experimental Pediatrics|February 19, 2026
Long-term outcome in children with infantile epileptic spasms syndrome: a multicenter retrospective study in KoreaSun Ah Choi, Minhye Kim, Hye Jin Kim, et al.
Journal of Epilepsy Research|January 28, 2015
Screening Autoimmune Anti-neuronal Antibodies in Pediatric Patients with Suspected Autoimmune EncephalitisSoo Yeon Kim, Sun Ah Choi, Hye Won Ryu, et al.
Journal of Movement Disorders|May 29, 2014
A case of isolated middle cerebral artery stenosis with hemichorea and moyamoya pattern collateralizationSeok Jong Chung, Hyung Seok Lee, Han Soo Yoo, et al.
Brain & Development|April 20, 2021
Early-onset autosomal dominant GTP-cyclohydrolase I deficiency: Diagnostic delay and residual motor signsWooJoong Kim, Jae So Cho, Young Kyu Shim, et al.
Annals of Laboratory Medicine|August 26, 2017
A Unique Mutational Spectrum of MLC1 in Korean Patients With Megalencephalic Leukoencephalopathy With Subcortical Cysts: p.Ala275Asp Founder Mutation and Maternal Uniparental Disomy of Chromosome 22Sun Ah Choi, Soo Yeon Kim, Jihoo Yoon, et al.
Epilepsy Research|December 4, 2017
Surgical outcome and predictive factors of epilepsy surgery in pediatric isolated focal cortical dysplasiaSun Ah Choi, Soo Yeon Kim, Hyuna Kim, et al.
Journal of Clinical Neurology (Seoul, Korea)|July 14, 2020
Clinical Spectrum of Myelin Oligodendrocyte Glycoprotein-Immunoglobulin G-Associated Disease in Korean ChildrenIl Han Yoo, WooJoong Kim, Youngkyu Shim, et al.
Pageof 7