Showing 1 - 20 results of 44 for search 'Jong‐Hee Chae', query time: 0.05s Refine Results
  1. 1
    A brain extraction algorithm for infant T2 weighted magnetic resonance images based on fuzzy c-means thresholding

    A brain extraction algorithm for infant T2 weighted magnetic resonance images based on fuzzy c-means thresholding by Inyoung Bae, Jong-Hee Chae, Yeji Han

    Published 2021-12-01
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  2. 2
    A compound heterozygous mutation in the gene: the first pediatric case causes fish odor syndrome in Korea

    A compound heterozygous mutation in the gene: the first pediatric case causes fish odor syndrome in Korea by Ji Hyun Kim, Sung Min Cho, Jong-Hee Chae

    Published 2017-03-01
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  3. 3
    Whole genomic approach in mutation discovery of infantile spasms patients

    Whole genomic approach in mutation discovery of infantile spasms patients by Seungbok Lee, Seungbok Lee, Sesong Jang, Jong-Il Kim, Jong-Il Kim, Jong Hee Chae, Jong Hee Chae, Ki Joong Kim, Byung Chan Lim

    Published 2022-07-01
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  4. 4
    The extended clinical and genetic spectrum of CTNNB1-related neurodevelopmental disorder

    The extended clinical and genetic spectrum of CTNNB1-related neurodevelopmental disorder by Seungbok Lee, Seungbok Lee, Se Song Jang, Soojin Park, Jihoon G. Yoon, Soo Yeon Kim, Soo Yeon Kim, Byung Chan Lim, Jong Hee Chae, Jong Hee Chae

    Published 2022-07-01
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  5. 5
    Successful Pallidal Deep Brain Stimulation in a Patient with Childhood-Onset Generalized Dystonia with ANO3 Mutation

    Successful Pallidal Deep Brain Stimulation in a Patient with Childhood-Onset Generalized Dystonia with ANO3 Mutation by Dallah Yoo, Han-Joon Kim, Jong-Hee Chae, Sun Ha Paek, Beomseok Jeon

    Published 2019-09-01
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  6. 6
    Neonatal-Onset Encephalopathy: A Rare Korean Case with Hypophosphatasia

    Neonatal-Onset Encephalopathy: A Rare Korean Case with Hypophosphatasia by Min Jun Chun, Yeon Sook Moon, Woo Ri Jang, Jong Hee Chae, Young Se Kwon

    Published 2022-01-01
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  7. 7
    Variable Phenotypes of ZC4H2-Associated Rare Disease in Six Patients

    Variable Phenotypes of ZC4H2-Associated Rare Disease in Six Patients by Ji Ye Ahn, Soo Yeon Kim, Byung Chan Lim, Ki Joong Kim, Jong-Hee Chae

    Published 2022-07-01
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  8. 8
    Nusinersen demonstrates effectiveness in treating spinal muscular atrophy: findings from a three-year nationwide study in Korea

    Nusinersen demonstrates effectiveness in treating spinal muscular atrophy: findings from a three-year nationwide study in Korea by Jaeso Cho, Jiwon Lee, Jihye Kim, Hyunjoo Lee, Min-Jee Kim, Yun Jeong Lee, Mi-Sun Yum, Ji-Hye Byun, Chong Guk Lee, Young-Mock Lee, Jeehun Lee, Jong-Hee Chae, Jong-Hee Chae

    Published 2023-12-01
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  9. 9
    Epilepsy phenotype and gene ontology analysis of the 129 genes in a large neurodevelopmental disorders cohort

    Epilepsy phenotype and gene ontology analysis of the 129 genes in a large neurodevelopmental disorders cohort by Young Jun Ko, Soo Yeon Kim, Soo Yeon Kim, Seungbok Lee, Jihoon G. Yoon, Man Jin Kim, Hyeji Jun, Hunmin Kim, Jong-Hee Chae, Jong-Hee Chae, Ki Joong Kim, Kwangsoo Kim, Byung Chan Lim

    Published 2023-08-01
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  10. 10
    Expanding the Clinical and Genetic Spectrum of Caveolinopathy in Korea

    Expanding the Clinical and Genetic Spectrum of Caveolinopathy in Korea by Seungbok Lee, Soo Yeon Kim, Byung Chan Lim, Ki Joong Kim, Jong Hee Chae, Anna Cho

    Published 2022-07-01
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  11. 11
    Pediatric Miller Fisher Syndrome; Characteristic Presentation and Comparison with Adult Miller Fisher Syndrome

    Pediatric Miller Fisher Syndrome; Characteristic Presentation and Comparison with Adult Miller Fisher Syndrome by Yeonji Jang, Jae-Hwan Choi, Jong Hee Chae, Byung Chan Lim, Seong-Joon Kim, Jae Ho Jung

    Published 2020-12-01
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  12. 12
    Genetic and clinical heterogeneity in Korean patients with Rubinstein–Taybi syndrome

    Genetic and clinical heterogeneity in Korean patients with Rubinstein–Taybi syndrome by Naye Choi, Hwa Young Kim, Byung Chan Lim, Jong‐Hee Chae, Soo Yeon Kim, Jung Min Ko

    Published 2021-10-01
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  13. 13
    Angiography-negative childhood primary angiitis of the central nervous system diagnosed by open brain biopsy: a case report

    Angiography-negative childhood primary angiitis of the central nervous system diagnosed by open brain biopsy: a case report by Dayun Kang, Soo Yeon Kim, Jong Hee Chae, Ki Joong Kim, Sung-Hye Park, Byung Chan Lim

    Published 2022-01-01
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  14. 14
    Short Course and Early Switch of Vigabatrin for Infantile spasms

    Short Course and Early Switch of Vigabatrin for Infantile spasms by Hye Won Ryu, Hunmin Kim, Byung Chan Lim, Hee Hwang, Jong-Hee Chae, Ji Eun Choi, Ki Joong Kim

    Published 2020-07-01
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  15. 15
    Home mechanical ventilation in childhood-onset hereditary neuromuscular diseases: 13 years' experience at a single center in Korea.

    Home mechanical ventilation in childhood-onset hereditary neuromuscular diseases: 13 years' experience at a single center in Korea. by Young Joo Han, June Dong Park, Bongjin Lee, Yu Hyeon Choi, Dong In Suh, Byung Chan Lim, Jong-Hee Chae

    Published 2015-01-01
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  16. 16
    Spectrum of movement disorders in GNAO1 encephalopathy: in-depth phenotyping and case-by-case analysis

    Spectrum of movement disorders in GNAO1 encephalopathy: in-depth phenotyping and case-by-case analysis by Soo Yeon Kim, YoungKyu Shim, Young Joon Ko, Soojin Park, Se Song Jang, Byung Chan Lim, Ki Joong Kim, Jong-Hee Chae

    Published 2020-12-01
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  17. 17
    A case of Becker muscular dystrophy with early manifestation of cardiomyopathy

    A case of Becker muscular dystrophy with early manifestation of cardiomyopathy by Ki Hyun Doo, Hye Won Ryu, Seung Soo Kim, Byung Chan Lim, Hui Hwang, Ki Joong Kim, Yong Seung Hwang, Jong-Hee Chae

    Published 2012-09-01
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  18. 18
    Deep Phenotyping in 1p36 Deletion Syndrome

    Deep Phenotyping in 1p36 Deletion Syndrome by Youngkyu Shim, Young Jun Go, Soo Yeon Kim, Hunmin Kim, Hee Hwang, Jieun Choi, Byung Chan Lim, Ki Joong Kim, Jong-Hee Chae

    Published 2020-10-01
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  19. 19
    Novel HEXA variants in Korean children with Tay–Sachs disease with regression of neurodevelopment from infancy

    Novel HEXA variants in Korean children with Tay–Sachs disease with regression of neurodevelopment from infancy by Ji Hong Park, Jung Min Ko, Min Sun Kim, Man Jin Kim, Moon‐Woo Seong, Taekyeong Yoo, Byung Chan Lim, Jong‐Hee Chae

    Published 2021-06-01
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  20. 20
    Expanding association between BICD2 variants and brain malformations and associated lissencephaly

    Expanding association between BICD2 variants and brain malformations and associated lissencephaly by Jaeso Cho, Haeryung Kim, Seoungbok Lee, Jihoon G Yoon, HyeJin Kim, Minhye Kim, Seoyun Jang, Woojoong Kim, Soo Yeon Kim, Jong Hee Chae

    Published 2024-01-01
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