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Korean Journal of Pediatrics|September 22, 2015
Successful sulfonylurea treatment in a patient with permanent neonatal diabetes mellitus with a novel KCNJ11 mutationSung Yeon Ahn, Gu-Hwan Kim, Han-Wook Yoo
Journal of the Korean Association of Oral and Maxillofacial Surgeons|August 29, 2023
Lesch-Nyhan syndrome: a case reportHan Ick Park, Gu-Hwan Kim, Kang-Min Ahn
Yonsei Medical Journal|December 17, 2014
The first Korean case of HDR syndrome confirmed by clinical and molecular investigationChong Kun Cheon, Gu Hwan Kim, Han Wook Yoo
Annals of Pediatric Endocrinology & Metabolism|April 23, 2016
Recent advances in biochemical and molecular analysis of congenital adrenal hyperplasia due to 21-hydroxylase deficiencyJin-Ho Choi, Gu-Hwan Kim, Han-Wook Yoo
Journal of Korean Medical Science|November 23, 2013
Clinical features of congenital adrenal insufficiency including growth patterns and significance of ACTH stimulation testJi Won Koh, Gu Hwan Kim, Han Wook Yoo, et al.
Jugan Geon-Gang Gwa Jilbyeong|December 3, 2025
[Developmental of a Support System for the Genetic Diagnosis and Counseling of Rare Disease]Gu-Hwan Kim, In-Hee Choi, Beom Hee Lee, et al.
Annals of Pediatric Endocrinology & Metabolism|July 4, 2023
Molecular basis and genetic testing strategies for diagnosing 21-hydroxylase deficiency, including CAH-X syndromeJa Hye Kim, Gu-Hwan Kim, Han-Wook Yoo, et al.
European Journal of Pediatrics|May 25, 2002
Identification of a novel mutation in the GLUT2 gene in a patient with Fanconi-Bickel syndrome presenting with neonatal diabetes mellitus and galactosaemiaHan-Wook Yoo, Young-Lim Shin, Eul-Ju Seo, et al.
Journal of Korean Medical Science|October 2, 2009
Familial glucocorticoid deficiency with a point mutation in the ACTH receptor: a case reportChan Jong Kim, Young Jong Woo, Gu Hwan Kim, et al.
Pediatric Neurology|July 12, 2014
OTC gene in ornithine transcarbamylase deficiency: clinical course and mutational spectrum in seven Korean patientsJung Hyun Lee, Gu-Hwan Kim, Han-Wook Yoo, et al.
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