Showing results (1-10 of 118) with videos related to
Sort By:
Pageof 12
Ewha Medical Journal|July 24, 2025
Management of Hyperphagia and Obesity in Prader-Willi SyndromeJiHoon Hwang, Sung Yoon ChoOsteoporosis and Sarcopenia|July 18, 2025
Hypophosphatasia in childhood: Diagnosis to managementMinji Im, Sung Yoon ChoAnnals of Pediatric Endocrinology & Metabolism|January 28, 2016
Guidelines for genetic skeletal dysplasias for pediatriciansSung Yoon Cho, Dong-Kyu JinIntractable & Rare Diseases Research|November 4, 2014
An overview of Korean patients with mucopolysaccharidosis and collaboration through the Asia Pacific MPS NetworkSung Yoon Cho, Young Bae Sohn, Dong-Kyu JinAnnals of Pediatric Endocrinology & Metabolism|January 7, 2022
Prader-Willi syndrome: an update on obesity and endocrine problemsSu Jin Kim, Sung Yoon Cho, Dong-Kyu JinOrphanet Journal of Rare Diseases|September 1, 2017
Prevalence and risk factors for type 2 diabetes mellitus with Prader-Willi syndrome: a single center experienceAram Yang, Jinsup Kim, Sung Yoon Cho, et al.Journal of Glaucoma|January 11, 2019
Clinical Characteristics of Autosomal Dominant GJA1 Missense Mutation Linked to Oculodentodigital Dysplasia in a Korean FamilyDo Young Park, Sung Yoon Cho, Dong-Kyu Jin, et al.Annals of Pediatric Endocrinology & Metabolism|July 21, 2015
Elevation of serum creatine kinase during methimazole treatment of Graves disease in a 13-year-old girl and a literature review of similar casesHyeseon Kim, Jinsup Kim, Rimm Huh, et al.Annals of Pediatric Endocrinology & Metabolism|July 5, 2018
Etiological trends in male central precocious pubertyJisun Lee, Jinsup Kim, Aram Yang, et al.Annals of Clinical and Laboratory Science|August 16, 2015
Letter to the Editor: A Novel Mutation in the CREBBP Gene of a Korean Girl with Rubinstein-Taybi syndromeRimm Huh, Sung Yoon Cho, Jinsup Kim, et al.Pageof 12