Chong-kun Cheon
Yangsan, Republic of Korea
Last Updated: 09/26/2026
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Found 9 publications
Clinical, endocrinological, and molecular features of four Korean cases of cytochrome P450 oxidoreductase deficiency.
Journal: Annals of pediatric endocrinology & metabolism
Published: September 11, 2019
A rare case of multiple pituitary adenomas in an adolescent Cushing disease presenting as a vertebral compression fracture.
Journal: Annals of pediatric endocrinology & metabolism
Published: February 06, 2017
Novel and Recurrent ACADS Mutations and Clinical Manifestations Observed in Korean Patients with Short-chain Acyl-coenzyme a Dehydrogenase Deficiency.
Journal: Annals of clinical and laboratory science
Published: July 29, 2016
Unravelling the mechanism of action of enzyme replacement therapy in Fabry disease.
Journal: Journal of human genetics
Published: July 28, 2015
Kabuki syndrome: clinical and molecular characteristics.
Journal: Korean journal of pediatrics
Published: March 25, 2015
Clinical outcomes and the mutation spectrum of the OTC gene in patients with ornithine transcarbamylase deficiency.
Journal: Journal of human genetics
Published: March 14, 2015
Vitamin D receptor gene polymorphisms and type 1 diabetes mellitus in a Korean population.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: July 26, 2014
NEU1 mutation in a Korean infant with type 2 sialidosis presenting as isolated fetal ascites.
Journal: Pediatrics and neonatology
Published: March 13, 2014
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Last Updated: 09/26/2026