Showing results (41-50 of 90) with videos related to
Sort By:
Pageof 9
Molecular Genetics and Metabolism Reports|March 4, 2022
Timing is everything: Clinical courses of Hunter syndrome associated with age at initiation of therapy in a sibling pairNathan Grant, Young Bae Sohn, N Matthew Ellinwood, et al.Journal of Korean Medical Science|August 2, 2016
Skin Barrier Function Is Not Impaired and Kallikrein 7 Gene Polymorphism Is Frequently Observed in Korean X-linked Ichthyosis Patients Diagnosed by Fluorescence in Situ Hybridization and Array Comparative Genomic HybridizationNoo Ri Lee, Na Young Yoon, Minyoung Jung, et al.Molecular Pharmaceutics|September 16, 2015
Pharmacokinetics, Pharmacodynamics, and Efficacy of a Novel Long-Acting Human Growth Hormone: Fc Fusion ProteinSu Jin Kim, Hyun-Hee Kwak, Sung Yoon Cho, et al.Journal of Korean Medical Science|May 8, 2012
Two novel insulin receptor gene mutations in a patient with Rabson-Mendenhall syndrome: the first Korean case confirmed by biochemical, and molecular evidenceDoosoo Kim, Sung Yoon Cho, Sung-Hee Yeau, et al.Annals of Clinical and Laboratory Science|February 29, 2012
A Korean patient with Morquio B disease with a novel c.13_14insA mutation in the GLB1 geneYoung Bae Sohn, Hyung-Doo Park, Sung Won Park, et al.Molecular Genetics and Metabolism Reports|January 18, 2024
Biomarkers of Glycosaminoglycans (GAG) accumulation in patients with mucopolysaccharidosis type VI-LeukoGAG, Corneal Opacification (COM) and Carotid Intima Media Thickening (CIMT)Young Bae Sohn, Raymond Wang, Jane Ashworth, et al.Yonsei Medical Journal|February 15, 2011
Delayed response of amylin levels after an oral glucose challenge in children with Prader-Willi syndromeHae Jeong Lee, Yon Ho Choe, Jee Hyun Lee, et al.Journal of Sleep Research|November 17, 2009
Plasma adiponectin level and sleep structures in children with Prader-Willi syndromeEun Yeon Joo, Seung Bong Hong, Young Bae Sohn, et al.Journal of Human Genetics|November 30, 2012
Clinical and genetic spectrum of 18 unrelated Korean patients with Sotos syndrome: frequent 5q35 microdeletion and identification of four novel NSD1 mutationsYoung Bae Sohn, Cha Gon Lee, Jung Min Ko, et al.The Journal of Clinical Endocrinology and Metabolism|January 12, 2010
Correlation of adiponectin receptor expression with cytokines and insulin sensitivity in growth hormone (GH)-treated children with Prader-Willi syndrome and in non-GH-treated obese childrenYoung Bae Sohn, Min Jung Kwak, Su Jin Kim, et al.Pageof 9