Search Results - Han-Wook Yoo

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  1. 1
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    Development of orphan drugs for rare diseases by Han-Wook Yoo

    Published 2024
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  2. 2
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    Diverse etiologies, diagnostic approach, and management of primary adrenal insufficiency in pediatric age by Han-Wook Yoo

    Published 2021
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  3. 3
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    Genetic testing in clinical pediatric practice by Han Wook Yoo

    Published 2010
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  4. 4
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    Management issues of congenital adrenal hyperplasia during the transition from pediatric to adult care by Jin-Ho Choi, Han-Wook Yoo

    Published 2017
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  5. 5
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    Growth hormone therapy in patients with Noonan syndrome by Go Hun Seo, Han-Wook Yoo

    Published 2018
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  6. 6
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    Successful sulfonylurea treatment in a patient with permanent neonatal diabetes mellitus with a novel mutation by Sung Yeon Ahn, Gu-Hwan Kim, Han-Wook Yoo

    Published 2015
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  7. 7
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    Recent advances in biochemical and molecular analysis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency by Jin-Ho Choi, Gu-Hwan Kim, Han-Wook Yoo

    Published 2016
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  8. 8
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    Three pediatric patients with primary hyperparathyroidism caused by parathyroid adenoma by Arum Oh, Yena Lee, Han-Wook Yoo, Jin-Ho Choi

    Published 2021
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  9. 9
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    Etiology and therapeutic outcomes of children with gonadotropin-independent precocious puberty by Eungu Kang, Ja Hyang Cho, Jin-Ho Choi, Han-Wook Yoo

    Published 2016
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  10. 10
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    Transient neonatal diabetes mellitus with macroglossia diagnosed by methylation specific PCR (MS-PCR) by Hye Young Jin, Jin-Ho Choi, Gu-Hwan Kim, Han-Wook Yoo

    Published 2010
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  11. 11
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    A case of thanatophoric dysplasia type I with an R248C mutation in the gene by Eun Jung Noe, Han Wook Yoo, Kwang Nam Kim, So Yeon Lee

    Published 2010
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  12. 12
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    Efficacy of growth hormone therapy in adults with childhood-onset growth hormone deficiency by Ja Hye Kim, Ja Hyang Cho, Han-Wook Yoo, Jin-Ho Choi

    Published 2014
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  13. 13
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    Molecular basis and genetic testing strategies for diagnosing 21-hydroxylase deficiency, including CAH-X syndrome by Ja Hye Kim, Gu-Hwan Kim, Han-Wook Yoo, Jin-Ho Choi

    Published 2023
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  14. 14
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    A family with Townes-Brocks syndrome with congenital hypothyroidism and a novel mutation of the gene by Won Ik Choi, Ji Hye Kim, Han Wook Yoo, Sung Hee Oh

    Published 2010
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  15. 15
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    Efficacy and safety of intravenous pamidronate infusion for treating osteoporosis in children and adolescents by Ji-Hee Yoon, Yunha Choi, Yena Lee, Han-Wook Yoo, Jin-Ho Choi

    Published 2021
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  16. 16
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    Efficacy and safety of parenteral vitamin D therapy in infants and children with vitamin D deficiency caused by intestinal malabsorption by Sae Bit Yu, Yena Lee, Arum Oh, Han-Wook Yoo, Jin-Ho Choi

    Published 2020
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  17. 17
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    Familial male-limited precocious puberty due to an activating mutation of the LHCGR: a case report and literature review by Jihyun Ha, Yunha Choi, Mo Kyung Jung, Eun-Gyong Yoo, Han-Wook Yoo

    Published 2024
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  18. 18
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    Pubertal outcomes and sex of rearing of patients with ovotesticular disorder of sex development and mixed gonadal dysgenesis by Yoon Myung Kim, Arum Oh, Kun-Suk Kim, Han-Wook Yoo, Jin-Ho Choi

    Published 2019
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  19. 19
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    p.R182C mutation in Korean twin with congenital lipoid adrenal hyperplasia by Hye Won Park, Byung Ok Kwak, Gu-Hwan Kim, Han-Wook Yoo, Sochung Chung

    Published 2013
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  20. 20
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    Compound heterozygous mutations of gene in newborn with short chain acyl-CoA dehydrogenase deficiency: case report and literatures review by Se Jin An, Sook Za Kim, Gu Hwan Kim, Han Wook Yoo, Han Hyuk Lim

    Published 2016
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