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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 mutation
Sung 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 report
Han 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 investigation
Chong 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 deficiency
Jin-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 test
Ji 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 syndrome
Ja 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 galactosaemia
Han-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 report
Chan 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 patients
Jung Hyun Lee, Gu-Hwan Kim, Han-Wook Yoo, et al.
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of 18
Search research articles
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Showing results (1-10 of 173) with videos related to
Sort By:
Page
of 18
Korean Journal of Pediatrics
|
September 22, 2015
Successful sulfonylurea treatment in a patient with permanent neonatal diabetes mellitus with a novel KCNJ11 mutation
Sung 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 report
Han 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 investigation
Chong 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 deficiency
Jin-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 test
Ji 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 syndrome
Ja 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 galactosaemia
Han-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 report
Chan 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 patients
Jung Hyun Lee, Gu-Hwan Kim, Han-Wook Yoo, et al.
Page
of 18