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Hyojin Chae

Showing results (21-30 of 89) with videos related to

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Scientific Reports|October 18, 2024
Dysbiosis of the initial stool microbiota increases the risk of developing necrotizing enterocolitis or feeding intolerance in newbornsHyojin Chae, Sae Yun Kim, Hyun Mi Kang, et al.
Journal of Pediatric and Adolescent Gynecology|January 22, 2013
Genotype and phenotype heterogeneity in perrault syndromeMin Jeong Kim, Sa Jin Kim, Jiyeon Kim, et al.
Clinical Biochemistry|May 14, 2021
Body fluid matrix effect evaluation on the Hitachi Labospect 008 systemHanwool Cho, Jin Jung, Jeong Joong Lee, et al.
Medicine|September 10, 2022
Laboratory characteristics of IgG4-related disease: A retrospective study from a single tertiary medical centerHanwool Cho, Jeong Joong Lee, Myungshin Kim, et al.
Annals of Pediatric Endocrinology & Metabolism|January 3, 2019
Nonautoimmune congenital hyperthyroidism due to p.Asp633Glu mutation in the TSHR geneWon Kyoung Cho, Moon-Bae Ahn, Woori Jang, et al.
Molecular Vision|November 26, 2015
Molecular analysis of the CHST6 gene in Korean patients with macular corneal dystrophy: Identification of three novel mutationsShin Hae Park, Ye Jin Ahn, Hyojin Chae, et al.
Journal of Clinical Laboratory Analysis|January 31, 2014
The analytical performance evaluation of Freelite™ Human Kappa Free and Human Lambda Free on the SPAPLUS™ immunoturbidimetric analyzerKyong-Ho Cha, Yang Bo Sim, Hyojin Chae, et al.
Annals of Laboratory Medicine|May 12, 2025
Diagnostic Performance of Eight Blood-based Biomarkers in a Well-characterized Korean Cohort of Preclinical Alzheimer's DiseaseHyojin Chae, Hyejeong Kim, Yoon-Joo Kim, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|June 8, 2020
Genotypic and phenotypic characteristics of Korean children with childhood-onset Leber's hereditary optic neuropathyYe Jin Ahn, Yooyeon Park, Sun Young Shin, et al.
The Journal of Obstetrics and Gynaecology Research|July 28, 2011
Prenatal diagnosis of autosomal recessive polycystic kidney disease by molecular genetic analysisDong Gyu Jang, Hyojin Chae, Jong Chul Shin, et al.
Pageof 9

Showing results (21-30 of 89) with videos related to

Sort By:
Pageof 9
Scientific Reports|October 18, 2024
Dysbiosis of the initial stool microbiota increases the risk of developing necrotizing enterocolitis or feeding intolerance in newbornsHyojin Chae, Sae Yun Kim, Hyun Mi Kang, et al.
Journal of Pediatric and Adolescent Gynecology|January 22, 2013
Genotype and phenotype heterogeneity in perrault syndromeMin Jeong Kim, Sa Jin Kim, Jiyeon Kim, et al.
Clinical Biochemistry|May 14, 2021
Body fluid matrix effect evaluation on the Hitachi Labospect 008 systemHanwool Cho, Jin Jung, Jeong Joong Lee, et al.
Medicine|September 10, 2022
Laboratory characteristics of IgG4-related disease: A retrospective study from a single tertiary medical centerHanwool Cho, Jeong Joong Lee, Myungshin Kim, et al.
Annals of Pediatric Endocrinology & Metabolism|January 3, 2019
Nonautoimmune congenital hyperthyroidism due to p.Asp633Glu mutation in the TSHR geneWon Kyoung Cho, Moon-Bae Ahn, Woori Jang, et al.
Molecular Vision|November 26, 2015
Molecular analysis of the CHST6 gene in Korean patients with macular corneal dystrophy: Identification of three novel mutationsShin Hae Park, Ye Jin Ahn, Hyojin Chae, et al.
Journal of Clinical Laboratory Analysis|January 31, 2014
The analytical performance evaluation of Freelite™ Human Kappa Free and Human Lambda Free on the SPAPLUS™ immunoturbidimetric analyzerKyong-Ho Cha, Yang Bo Sim, Hyojin Chae, et al.
Annals of Laboratory Medicine|May 12, 2025
Diagnostic Performance of Eight Blood-based Biomarkers in a Well-characterized Korean Cohort of Preclinical Alzheimer's DiseaseHyojin Chae, Hyejeong Kim, Yoon-Joo Kim, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|June 8, 2020
Genotypic and phenotypic characteristics of Korean children with childhood-onset Leber's hereditary optic neuropathyYe Jin Ahn, Yooyeon Park, Sun Young Shin, et al.
The Journal of Obstetrics and Gynaecology Research|July 28, 2011
Prenatal diagnosis of autosomal recessive polycystic kidney disease by molecular genetic analysisDong Gyu Jang, Hyojin Chae, Jong Chul Shin, et al.
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