Showing results (41-50 of 65) with videos related to

Sort By:
Pageof 7
Annals of Pediatric Endocrinology & Metabolism|April 18, 2015
Clinical, endocrinological, and molecular characterization of Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism: a single center experienceSun-Jeong Shin, Yeonah Sul, Ja Hye Kim, et al.
Korean Journal of Pediatrics|February 20, 2016
Identification of 1p36 deletion syndrome in patients with facial dysmorphism and developmental delayGo Hun Seo, Ja Hye Kim, Ja Hyang Cho, et al.
Endocrine Connections|March 14, 2023
Mutation spectrum and frequency of copy number variations of the ANOS1 gene in patients with Kallmann syndrome or normosmic isolated hypogonadotropic hypogonadismJa Hye Kim, Yunha Choi, Soojin Hwang, et al.
Annals of Pediatric Endocrinology & Metabolism|January 25, 2024
Long-term endocrine sequelae after hematopoietic stem cell transplantation in children and adolescentsSoojin Hwang, Yena Lee, Ji-Hee Yoon, et al.
Endocrine Journal|November 12, 2025
Diagnostic criteria for acquired hypothalamic obesity - international expert guidance documentHermann L Müller, Tomohiro Tanaka, Tomonobu Hasegawa, et al.
Molecular and Cellular Endocrinology|January 29, 2017
Diagnostic yield of targeted gene panel sequencing to identify the genetic etiology of disorders of sex developmentJa Hye Kim, Eungu Kang, Sun Hee Heo, et al.
BMC Medical Genomics|May 16, 2026
Long-term safety and efficacy of triheptanoin in Korean patients with long-chain fatty acid oxidation disorders: a prospective, open-label, single-center, phase II clinical studyJi-Hee Yoon, Jun-Hong Park, Dohyung Kim, et al.
Annals of Neurology|January 26, 2023
Ultra-Low Level Somatic Mutations and Structural Variations in Focal Cortical Dysplasia Type IIJa Hye Kim, Ji-Hyung Park, Junehawk Lee, et al.
Medicine|September 20, 2022
A phase II, multicenter, open-label trial to evaluate the safety and efficacy of ISU303 (Agalsidase beta) in patients with Fabry diseaseSoojin Hwang, Beom Hee Lee, Woo-Shik Kim, et al.
Journal of Human Genetics|May 22, 2015
Clinical outcomes and the mutation spectrum of the OTC gene in patients with ornithine transcarbamylase deficiencyJin-Ho Choi, Beom Hee Lee, Ja Hye Kim, et al.
Pageof 7