Search Results - Woo Yeong Chung

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  1. 1
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    A 10-year-old Boy with Microscopic Hematuria and Renal Biopsy Findings Mimicking Fabry Disease by Woo Yeong Chung, Mi Seon Kang

    Published 2016
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  2. 2
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    Changes in the thyroid hormone profiles in children with nephrotic syndrome by Sun Hee Jung, Jeong Eun Lee, Woo Yeong Chung

    Published 2019
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  3. 3
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    Insulin autoimmune syndrome induced by methimazole in a Korean girl with Graves' disease by Sun Hee Lee, Seung Hwan Oh, Woo Yeong Chung

    Published 2013
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  4. 4
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    Novel Mutations and Genetic Characterization in Korean Patients with Familial Renal Glucosuria by Weon Kyung Lee, Seung Hwan Oh, Woo Yeong Chung

    Published 2018
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  5. 5
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    Renal Problems in Early Adult Patients with Turner Syndrome by Dong Uk Yu, Jae Kyun Ku, Woo Yeong Chung

    Published 2015
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  6. 6
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    A Novel Nonsense Variant in the BCL11A Gene in a Male Patient with Intellectual Disability and Epilepsy by Seung Ho Kim, Go Hun Seo, Seung Hwan Oh, Woo Yeong Chung, Jeesuk Yu

    Published 2023
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  7. 7
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    A Mutation Underlying Mega-Corpus Callosum Syndrome with Extended Phenotypes: The First Case in Korea by Yun Jung Hur, Woo Yeong Chung, Yun-Jung Lim, Sooyoung Park, Kyung Ran Jun

    Published 2021
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  8. 8
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    Effects of long-term growth hormone therapy in a girl with Floating-Harbor syndrome by Hyun Woo Son, Jeong Eun Lee, Seung Hwan Oh, Changwon Keum, Woo Yeong Chung

    Published 2020
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  9. 9
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    Identification of a heterozygous ACAN mutation in a 15-year-old boy with short stature who presented with advanced bone age: a case report and review of the literature by Tae Youp Kim, Kyung Mi Jang, Chang Won Keum, Seung Hwan Oh, Woo Yeong Chung

    Published 2020
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  10. 10
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    A Rare Case of Hyponatremia Caused by Reset Osmostat in a Neonate with Cleft Lip, Cleft Palate, and Imperforate Anus by Jung Gu Ahn, Jeong Eun Lee, Woo Yeong Chung, Soo Hyun Koo, Jaeho Shin, Ga Won Jeon

    Published 2018
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  11. 11
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    Morning Glory Syndrome associated with Autosomal Dominant Alport Syndrome with a Heterozygous Mutation by So Jeong Kim, Jeong Eun Lee, Hyun Duck Kwak, Mi Seon Kang, Seong Ah Yu, Go Hun Seo, Seung Hwan Oh, Woo Yeong Chung

    Published 2021
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  12. 12
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    An A627V-activating mutation in the thyroid-stimulating hormone receptor gene in familial non-autoimmune hyperthyroidism by Jung Hyun Shin, Go Hun Seo, Seung Hwan Oh, Woo Yeong Chung, Hye Young Kim, Young Mi Kim, Mi Hye Bae, Kyung Hee Park, Min Jung Kwak

    Published 2020
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  13. 13
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    The influence of gonadotropin releasing hormone agonist treatment on the body weight and body mass index in girls with idiopathic precocious puberty and early puberty by Sung Woo Kim, Young Bae Kim, Jeong Eun Lee, Na Ri Kim, Weon Kyung Lee, Jae Kyun Ku, Eun Jeong Kim, Sun Hee Jung, Woo Yeong Chung

    Published 2017
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  14. 14
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    Response to growth hormone according to provocation test results in idiopathic short stature and idiopathic growth hormone deficiency by Ju Young Yoon, Chong Kun Cheon, Jung Hyun Lee, Min Jung Kwak, Hyun-Ji Kim, Ye Jin Kim, Jeong Eun Lee, Woo Yeong Chung, Jeongyun Kim, Jae-Ho Yoo

    Published 2022
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  15. 15
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    Incidence trends and associated factors of diabetes mellitus in Korean children and adolescents: a retrospective cohort study in Busan and Gyeongnam by Jung Hyun Lee, Yu-Mi Kim, Min Jung Kwak, Su Yung Kim, Hyun-Ji Kim, Chong Kun Cheon, Woo Yeong Chung, Im-Jeong Choi, Su Young Hong, Hee Won Chueh, Jae-Ho Yoo

    Published 2015
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  16. 16
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    Clinical use of whole exome sequencing in children with developmental delay/intellectual disability by Yoon Hee Jo, Soo Han Choi, Hye Won Yoo, Min Jung Kwak, Kyung Hee Park, Juhyun Kong, Yun-Jin Lee, Sang Ook Nam, Bo Lyun Lee, Woo Yeong Chung, Seung Hwan Oh, Young Mi Kim

    Published 2024
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