Sökresultat - Han-Wook Yoo

Development of orphan drugs for rare diseases av Han-Wook Yoo

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Diverse etiologies, diagnostic approach, and management of primary adrenal insufficiency in pediatric age av Han-Wook Yoo

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Genetic testing in clinical pediatric practice av Han Wook Yoo

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Management issues of congenital adrenal hyperplasia during the transition from pediatric to adult care av Jin-Ho Choi, Han-Wook Yoo

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Growth hormone therapy in patients with Noonan syndrome av Go Hun Seo, Han-Wook Yoo

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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