Dong-kyu K. Jin

Suwon, Republic of Korea

Last Updated: 09/26/2026

Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 112 publications

Systemic AAV-hGCDH Gene Therapy Alleviates Glutaric Acid Accumulation and Attenuates Chronic Brain Vacuolation in a Novel Mouse Model of Glutaric Aciduria Type I.

Systemic AAV-hGCDH Gene Therapy Alleviates Glutaric Acid Accumulation and Attenuates Chronic Brain Vacuolation in a Novel Mouse Model of Glutaric Aciduria Type I.

Journal: International journal of molecular sciences
Published: May 13, 2026

Efficacy and safety of idursulfase beta in the treatment of mucopolysaccharidosis II: A phase-3, 2-part study compared with a historical placebo cohort.

Efficacy and safety of idursulfase beta in the treatment of mucopolysaccharidosis II: A phase-3, 2-part study compared with a historical placebo cohort.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: October 22, 2024

The Youngest Infant to Be Diagnosed with Autosomal Dominant Hypocalcemia Type 2 Harboring a Novel Variant of GNA11: A Case Study and Literature Review.

The Youngest Infant to Be Diagnosed with Autosomal Dominant Hypocalcemia Type 2 Harboring a Novel Variant of GNA11: A Case Study and Literature Review.

Journal: Annals of clinical and laboratory science
Published: July 01, 2022

The longitudinal effect of oxcarbazepine on thyroid function in children and adolescents with epilepsy.

The longitudinal effect of oxcarbazepine on thyroid function in children and adolescents with epilepsy.

Journal: Epilepsia
Published: April 21, 2022

Natural History and Molecular Characteristics of Korean Patients with Mucopolysaccharidosis Type III.

Natural History and Molecular Characteristics of Korean Patients with Mucopolysaccharidosis Type III.

Journal: Journal of personalized medicine
Published: March 27, 2022

Endocrine and Metabolic Illnesses in Young Adults with Prader-Willi Syndrome.

Endocrine and Metabolic Illnesses in Young Adults with Prader-Willi Syndrome.

Journal: Journal of personalized medicine
Published: March 26, 2022

Late-infantile GM1 gangliosidosis: A case report.

Late-infantile GM1 gangliosidosis: A case report.

Journal: Medicine
Published: November 25, 2021

Development and validation of the Pediatric-Youth Hyperphagia Assessment for Prader-Willi syndrome.

Development and validation of the Pediatric-Youth Hyperphagia Assessment for Prader-Willi syndrome.

Journal: Epidemiology and health
Published: November 19, 2021

Prader-Willi syndrome: an update on obesity and endocrine problems.

Prader-Willi syndrome: an update on obesity and endocrine problems.

Journal: Annals of pediatric endocrinology & metabolism
Published: August 16, 2021

Recombinant growth hormone therapy in children with Turner Syndrome in Korea: a phase III Randomized Trial.

Recombinant growth hormone therapy in children with Turner Syndrome in Korea: a phase III Randomized Trial.

Journal: BMC endocrine disorders
Published: July 31, 2021

First female Korean child with Coffin-Lowry syndrome: a novel variant in RPS6KA3 diagnosed by exome sequencing and a literature review.

First female Korean child with Coffin-Lowry syndrome: a novel variant in RPS6KA3 diagnosed by exome sequencing and a literature review.

Journal: Annals of pediatric endocrinology & metabolism
Published: June 28, 2021

Appropriate Age for Height Control Treatment in Patients With Marfan Syndrome.

Appropriate Age for Height Control Treatment in Patients With Marfan Syndrome.

Journal: Frontiers in endocrinology
Published: May 12, 2021
Showing 1-12 of 112

Last Updated: 09/26/2026