Yunha Choi
Seoul, Republic of Korea
Last Updated: 09/26/2026
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Found 18 publications
Clinical Characteristics and Long-Term Outcomes of Adrenal Tumors in Children and Adolescents.
Journal: Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association
Published: July 12, 2023
Mutation spectrum and frequency of copy number variations of the ANOS1 gene in patients with Kallmann syndrome or normosmic isolated hypogonadotropic hypogonadism.
Journal: Endocrine connections
Published: March 01, 2023
A phase II, multicenter, open-label trial to evaluate the safety and efficacy of ISU303 (Agalsidase beta) in patients with Fabry disease.
Journal: Medicine
Published: September 20, 2022
Clinical and genetic analyses of patients with lateralized overgrowth.
Journal: BMC medical genomics
Published: June 01, 2022
Identification of a novel therapeutic target underlying atypical manifestation of Gaucher disease.
Journal: Clinical and translational medicine
Published: January 17, 2022
Metabolic Impacts of Discontinuation and Resumption of Recombinant Human Growth Hormone Treatment during the Transition Period in Patients with Childhood-Onset Growth Hormone Deficiency.
Journal: Endocrinology and metabolism (Seoul, Korea)
Published: December 27, 2021
Diagnostic performance of automated, streamlined, daily updated exome analysis in patients with neurodevelopmental delay.
Journal: Molecular medicine (Cambridge, Mass.)
Published: December 23, 2021
Phenotypic spectrum of patients with mutations in CHD7: clinical implications of endocrinological findings.
Journal: Endocrine connections
Published: December 18, 2021
Unfavorable clinical outcomes in patients with carbamoyl phosphate synthetase 1 deficiency.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: November 08, 2021
Whole-body MRI evaluation in neurofibromatosis type 1 patients younger than 3 years old and the genetic contribution to disease progression.
Journal: Orphanet journal of rare diseases
Published: August 31, 2021
Genotype-phenotype correlations and long-term efficacy of pamidronate therapy in patients with osteogenesis imperfecta.
Journal: Annals of pediatric endocrinology & metabolism
Published: July 19, 2021
Phenotypic and molecular spectra of patients with switch/sucrose nonfermenting complex-related intellectual disability disorders in Korea.
Journal: BMC medical genomics
Published: May 12, 2021
Last Updated: 09/26/2026