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Journal of Clinical Neurology (Seoul, Korea)
|
October 9, 2019
Elevated Serum Uric Acid in Benign Convulsions with Mild Gastroenteritis in Children
Il Han Yoo, Woojoong Kim, Jaeso Cho, et al.
Lab on a Chip
|
September 3, 2019
Dynamics of driftless preconcentration using ion concentration polarization leveraged by convection and diffusion
Seongho Baek, Jihye Choi, Seok Young Son, et al.
Orphanet Journal of Rare Diseases
|
December 10, 2020
Spectrum of movement disorders in GNAO1 encephalopathy: in-depth phenotyping and case-by-case analysis
Soo Yeon Kim, YoungKyu Shim, Young Joon Ko, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)
|
September 23, 2010
Relapsing demyelinating CNS disease in a Korean pediatric population: multiple sclerosis versus neuromyelitis optica
Byung Chan Lim, Hee Hwang, Ki Joong Kim, et al.
Orphanet Journal of Rare Diseases
|
September 7, 2024
Genetic profiling and diagnostic strategies for patients with ectodermal dysplasias in Korea
Man Jin Kim, Jee-Soo Lee, Seung Won Chae, et al.
Molecular Genetics & Genomic Medicine
|
April 3, 2021
Novel HEXA variants in Korean children with Tay-Sachs disease with regression of neurodevelopment from infancy
Ji Hong Park, Jung Min Ko, Min Sun Kim, et al.
Journal of Rheumatic Diseases
|
July 21, 2023
A Patient With Late-onset Limb-girdle Muscular Dystrophy Type 2B Mimicking Dermatomyositis: A Case Report and Review
Min Jung Kim, Yoon-Jeong Oh, Yoon Ho Hong, et al.
Annals of Laboratory Medicine
|
January 2, 2015
Non-homologous end joining repair mechanism-mediated deletion of CHD7 gene in a patient with typical CHARGE syndrome
Seung Jun Lee, Jong Hee Chae, Jung Ae Lee, et al.
Journal of Clinical Neurology (Seoul, Korea)
|
September 11, 2018
Paroxysmal Dyskinesia in Children: from Genes to the Clinic
Soo Yeon Kim, Jin Sook Lee, Woo Joong Kim, et al.
BMC Ophthalmology
|
November 4, 2025
Ophthalmologic manifestations associated with Fukutin (FKTN) variant subtypes in Korean patients with Fukuyama congenital muscular dystrophy: a single-center retrospective case series
Seok Jae Lee, Hye Jun Joo, Dong Hyun Jo, et al.
Page
of 26
Search research articles
Search
Showing results (81-90 of 256) with videos related to
Sort By:
Page
of 26
Journal of Clinical Neurology (Seoul, Korea)
|
October 9, 2019
Elevated Serum Uric Acid in Benign Convulsions with Mild Gastroenteritis in Children
Il Han Yoo, Woojoong Kim, Jaeso Cho, et al.
Lab on a Chip
|
September 3, 2019
Dynamics of driftless preconcentration using ion concentration polarization leveraged by convection and diffusion
Seongho Baek, Jihye Choi, Seok Young Son, et al.
Orphanet Journal of Rare Diseases
|
December 10, 2020
Spectrum of movement disorders in GNAO1 encephalopathy: in-depth phenotyping and case-by-case analysis
Soo Yeon Kim, YoungKyu Shim, Young Joon Ko, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)
|
September 23, 2010
Relapsing demyelinating CNS disease in a Korean pediatric population: multiple sclerosis versus neuromyelitis optica
Byung Chan Lim, Hee Hwang, Ki Joong Kim, et al.
Orphanet Journal of Rare Diseases
|
September 7, 2024
Genetic profiling and diagnostic strategies for patients with ectodermal dysplasias in Korea
Man Jin Kim, Jee-Soo Lee, Seung Won Chae, et al.
Molecular Genetics & Genomic Medicine
|
April 3, 2021
Novel HEXA variants in Korean children with Tay-Sachs disease with regression of neurodevelopment from infancy
Ji Hong Park, Jung Min Ko, Min Sun Kim, et al.
Journal of Rheumatic Diseases
|
July 21, 2023
A Patient With Late-onset Limb-girdle Muscular Dystrophy Type 2B Mimicking Dermatomyositis: A Case Report and Review
Min Jung Kim, Yoon-Jeong Oh, Yoon Ho Hong, et al.
Annals of Laboratory Medicine
|
January 2, 2015
Non-homologous end joining repair mechanism-mediated deletion of CHD7 gene in a patient with typical CHARGE syndrome
Seung Jun Lee, Jong Hee Chae, Jung Ae Lee, et al.
Journal of Clinical Neurology (Seoul, Korea)
|
September 11, 2018
Paroxysmal Dyskinesia in Children: from Genes to the Clinic
Soo Yeon Kim, Jin Sook Lee, Woo Joong Kim, et al.
BMC Ophthalmology
|
November 4, 2025
Ophthalmologic manifestations associated with Fukutin (FKTN) variant subtypes in Korean patients with Fukuyama congenital muscular dystrophy: a single-center retrospective case series
Seok Jae Lee, Hye Jun Joo, Dong Hyun Jo, et al.
Page
of 26