Chong K. Cheon

Yangsan, Republic of Korea

Last Updated: 09/26/2026

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Found 72 publications

Ocular manifestations in DYRK1A mutation: a five-case series from South Korea.

Ocular manifestations in DYRK1A mutation: a five-case series from South Korea.

Journal: Ophthalmic genetics

Published: March 10, 2026

Genetic characteristics and clinical features of pediatric congenital adrenal hyperplasia in Korea.

Genetic characteristics and clinical features of pediatric congenital adrenal hyperplasia in Korea.

Journal: Endocrine

Published: March 04, 2026

Gomisin N Improves Insulin Secretion by Alleviating Endoplasmic Reticulum and Oxidative Stress in Pancreatic Beta Cells.

Gomisin N Improves Insulin Secretion by Alleviating Endoplasmic Reticulum and Oxidative Stress in Pancreatic Beta Cells.

Journal: International journal of endocrinology

Published: February 13, 2026

PRPS1 (p.V42L) Mutation in Arts Syndrome Induces Aberrant Neural Stem Cell Development and Neuronal Senescence-Like Phenotype: Rescue by Nicotinamide Mononucleotide Supplementation.

PRPS1 (p.V42L) Mutation in Arts Syndrome Induces Aberrant Neural Stem Cell Development and Neuronal Senescence-Like Phenotype: Rescue by Nicotinamide Mononucleotide Supplementation.

Journal: International journal of stem cells

Published: December 04, 2025

Clinical Characteristics and Follow-up Course of 17α-Hydroxylase/17,20-Lyase Deficiency in Korea: the OUTSPREAD Multicenter Study.

Clinical Characteristics and Follow-up Course of 17α-Hydroxylase/17,20-Lyase Deficiency in Korea: the OUTSPREAD Multicenter Study.

Journal: Endocrinology and metabolism (Seoul, Korea)

Published: October 10, 2025

Exploring the Impact of RNU4-2 Defects on Neurodevelopmental Disorders in a Korean Population.

Exploring the Impact of RNU4-2 Defects on Neurodevelopmental Disorders in a Korean Population.

Journal: Clinical genetics

Published: September 23, 2025

Unmasking delayed recovery in severe diabetic ketoacidosis: clinical and biochemical clues from early resuscitation.

Unmasking delayed recovery in severe diabetic ketoacidosis: clinical and biochemical clues from early resuscitation.

Journal: Annals of pediatric endocrinology & metabolism

Published: August 29, 2025

Perivascular spaces and basilar artery remodeling in Fabry disease-a dual vascular pathology.

Perivascular spaces and basilar artery remodeling in Fabry disease-a dual vascular pathology.

Journal: Frontiers in neurology

Published: August 20, 2025

Clinical Characteristics and Outcomes of Korean Patients with Lipoid Congenital Adrenal Hyperplasia: An Analysis of Data from the Multicenter Networks for Ideal Outcomes of Pediatric Rare Endocrine and Metabolic Disease (OUTSPREAD) Cohort Study.

Clinical Characteristics and Outcomes of Korean Patients with Lipoid Congenital Adrenal Hyperplasia: An Analysis of Data from the Multicenter Networks for Ideal Outcomes of Pediatric Rare Endocrine and Metabolic Disease (OUTSPREAD) Cohort Study.

Journal: Endocrinology and metabolism (Seoul, Korea)

Published: August 19, 2025

Achievements and Expectations of the Rare Disease Diagnostic Support Program in the Republic of Korea

Achievements and Expectations of the Rare Disease Diagnostic Support Program in the Republic of Korea

Journal: Jugan geon-gang gwa jilbyeong

Published: June 16, 2025

Multidisciplinary Care Model as a Center of Excellence for Fabry Disease: A Practical Guide to Diagnosis and Management by Clinical Specialty in South Korea.

Multidisciplinary Care Model as a Center of Excellence for Fabry Disease: A Practical Guide to Diagnosis and Management by Clinical Specialty in South Korea.

Journal: Journal of clinical medicine

Published: May 11, 2025

Congenital hyperinsulinism due to NEUROD1 gene mutation.

Congenital hyperinsulinism due to NEUROD1 gene mutation.

Journal: Annals of pediatric endocrinology & metabolism

Published: February 01, 2025

Showing 1-12 of 72

Last Updated: 09/26/2026