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Byung Chan Lim

Showing results (61-70 of 173) with videos related to

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Journal of Clinical Neurology (Seoul, Korea)|October 9, 2019
Elevated Serum Uric Acid in Benign Convulsions with Mild Gastroenteritis in ChildrenIl Han Yoo, Woojoong Kim, Jaeso Cho, et al.
Clinical Genetics|December 22, 2020
Genetic diagnosis of infantile-onset epilepsy in the clinic: Application of whole-exome sequencing following epilepsy gene panel testingSoo Yeon Kim, Se Song Jang, Hunmin Kim, et al.
Journal of Clinical Neurology (Seoul, Korea)|January 17, 2020
Erratum to: Elevated Serum Uric Acid in Benign Convulsions with Mild Gastroenteritis in ChildrenIl Han Yoo, Woojoong Kim, Jaeso Cho, et al.
Frontiers in Neurology|October 2, 2019
Diagnostic Yield of Epilepsy Panel Testing in Patients With Seizure Onset Within the First Year of LifeSe Song Jang, Soo Yeon Kim, Hunmin Kim, et al.
Orphanet Journal of Rare Diseases|December 10, 2020
Spectrum of movement disorders in GNAO1 encephalopathy: in-depth phenotyping and case-by-case analysisSoo Yeon Kim, YoungKyu Shim, Young Joon Ko, et al.
Scientific Reports|October 14, 2025
Expanding the clinical and genetic spectrum of GLUL-related developmental and epileptic encephalopathyDong Eon Oh, Se Song Jang, Woo Joong Kim, et al.
Korean Journal of Pediatrics|October 11, 2012
A case of Becker muscular dystrophy with early manifestation of cardiomyopathyKi Hyun Doo, Hye Won Ryu, Seung Soo Kim, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|September 23, 2010
Relapsing demyelinating CNS disease in a Korean pediatric population: multiple sclerosis versus neuromyelitis opticaByung Chan Lim, Hee Hwang, Ki Joong Kim, et al.
Brain Pathology (Zurich, Switzerland)|October 31, 2018
A 3-Month-Old Boy With Progressive WeaknessSoo Yeon Kim, Jung Min Ko, Sun Ah Choi, et al.
Molecular Genetics & Genomic Medicine|April 3, 2021
Novel HEXA variants in Korean children with Tay-Sachs disease with regression of neurodevelopment from infancyJi Hong Park, Jung Min Ko, Min Sun Kim, et al.
Pageof 18

Showing results (61-70 of 173) with videos related to

Sort By:
Pageof 18
Journal of Clinical Neurology (Seoul, Korea)|October 9, 2019
Elevated Serum Uric Acid in Benign Convulsions with Mild Gastroenteritis in ChildrenIl Han Yoo, Woojoong Kim, Jaeso Cho, et al.
Clinical Genetics|December 22, 2020
Genetic diagnosis of infantile-onset epilepsy in the clinic: Application of whole-exome sequencing following epilepsy gene panel testingSoo Yeon Kim, Se Song Jang, Hunmin Kim, et al.
Journal of Clinical Neurology (Seoul, Korea)|January 17, 2020
Erratum to: Elevated Serum Uric Acid in Benign Convulsions with Mild Gastroenteritis in ChildrenIl Han Yoo, Woojoong Kim, Jaeso Cho, et al.
Frontiers in Neurology|October 2, 2019
Diagnostic Yield of Epilepsy Panel Testing in Patients With Seizure Onset Within the First Year of LifeSe Song Jang, Soo Yeon Kim, Hunmin Kim, et al.
Orphanet Journal of Rare Diseases|December 10, 2020
Spectrum of movement disorders in GNAO1 encephalopathy: in-depth phenotyping and case-by-case analysisSoo Yeon Kim, YoungKyu Shim, Young Joon Ko, et al.
Scientific Reports|October 14, 2025
Expanding the clinical and genetic spectrum of GLUL-related developmental and epileptic encephalopathyDong Eon Oh, Se Song Jang, Woo Joong Kim, et al.
Korean Journal of Pediatrics|October 11, 2012
A case of Becker muscular dystrophy with early manifestation of cardiomyopathyKi Hyun Doo, Hye Won Ryu, Seung Soo Kim, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|September 23, 2010
Relapsing demyelinating CNS disease in a Korean pediatric population: multiple sclerosis versus neuromyelitis opticaByung Chan Lim, Hee Hwang, Ki Joong Kim, et al.
Brain Pathology (Zurich, Switzerland)|October 31, 2018
A 3-Month-Old Boy With Progressive WeaknessSoo Yeon Kim, Jung Min Ko, Sun Ah Choi, et al.
Molecular Genetics & Genomic Medicine|April 3, 2021
Novel HEXA variants in Korean children with Tay-Sachs disease with regression of neurodevelopment from infancyJi Hong Park, Jung Min Ko, Min Sun Kim, et al.
Pageof 18