Ha Y. Jo
Busan, Republic of Korea
Last Updated: 09/26/2026
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Found 11 publications
X-linked spondyloepiphyseal dysplasia tarda misdiagnosed as growth hormone deficiency: identification of a novel intronic TRAPPC2 variant by whole-genome sequencing.
Journal: BMC pediatrics
Published: February 09, 2026
Extracellular vesicles for macrophage reprogramming: an emerging paradigm in immunomodulatory therapeutics.
Journal: Journal of biological engineering
Published: September 29, 2025
Comparison of growth hormone therapy response according to the presence of growth hormone deficiency in children born small for gestational age with short stature in Korea: a retrospective cohort study.
Journal: BMC pediatrics
Published: September 10, 2024
Pontocerebellar Hypoplasia 7 with Novel Compound Heterozygous Variants of TOE1 in a Boy with Micropenis, Developmental Delay, and Ataxia: The First Korean Case Report.
Journal: Annals of clinical and laboratory science
Published: November 09, 2023
Adult height in girls with central precocious puberty without gonadotropin-releasing hormone agonist treatment: a retrospective case-control study.
Journal: Journal of Yeungnam medical science
Published: July 13, 2023
Orbital apex syndrome in pediatric thyroid eye disease: a case report and literature review.
Journal: Annals of pediatric endocrinology & metabolism
Published: May 24, 2023
Turner syndrome due to Xp22.33 deletion combined with 7p22.3 duplication.
Journal: Annals of pediatric endocrinology & metabolism
Published: May 17, 2022
Incidence of congenital hypothyroidism by gestational age: a retrospective observational study.
Journal: Journal of Yeungnam medical science
Published: January 25, 2022
Effect of gonadotropin-releasing hormone agonist treatment on near final height in girls with central precocious puberty and early puberty.
Journal: Annals of pediatric endocrinology & metabolism
Published: December 05, 2021
Clinical and Laboratory Characteristics of Kikuchi-Fujimoto Disease According to Age.
Journal: Frontiers in pediatrics
Published: July 22, 2021
Identification of a novel variant in the PHEX gene using targeted gene panel sequencing in a 24-month-old boy with hypophosphatemic rickets.
Journal: Annals of pediatric endocrinology & metabolism
Published: March 29, 2019
Showing 1-11 of 11
Last Updated: 09/26/2026