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American Journal of Medical Genetics. Part A|November 23, 2011
Retrospective analysis of the clinical manifestations and survival of Korean patients with mucopolysaccharidosis type II: emphasis on the cardiovascular complication and mortality casesYoung Bae Sohn, Eun Wha Choi, Su Jin Kim, et al.
Journal of Korean Medical Science|February 20, 2014
Impact of enzyme replacement therapy on linear growth in Korean patients with mucopolysaccharidosis type II (Hunter syndrome)Sung Yoon Cho, Rimm Huh, Mi Sun Chang, et al.
American Journal of Medical Genetics. Part A|November 5, 2011
A polymorphism in the growth hormone receptor is associated with height in children with Prader-Willi syndromeSung Won Park, Seung-Tae Lee, Young Bae Sohn, et al.
Endocrinology|July 9, 2010
Differential effects of insufflated, subcutaneous, and intravenous growth hormone on bone growth, cognitive function, and NMDA receptor subunit expressionSung Won Park, Sooyoung Shin, Chi Hwa Kim, et al.
Annals of Clinical and Laboratory Science|February 18, 2011
Mutations of ACADS gene associated with short-chain acyl-coenzyme A dehydrogenase deficiencySe Hwa Kim, Hyung-Doo Park, Young Bae Sohn, et al.
Yonsei Medical Journal|May 3, 2008
Outcome following surgical closure of patent ductus arteriosus in very low birth weight infants in neonatal intensive care unitGa Yeun Lee, Young Bae Sohn, Myo Jing Kim, et al.
Digestive Surgery|March 12, 2009
Serum obestatin/ghrelin ratio is altered in patients after distal gastrectomySung Kim, Jun Haeng Lee, Jin Seok Heo, et al.
European Journal of Medical Genetics|December 28, 2014
Case of mild Schmid-type metaphyseal chondrodysplasia with novel sequence variation involving an unusual mutational site of the COL10A1 geneHyunwoong Park, Susie Hong, Sung Im Cho, et al.
American Journal of Medical Genetics. Part A|April 13, 2012
Enzyme replacement therapy improves joint motion and outcome of the 12-min walk test in a mucopolysaccharidosis type VI patient previously treated with bone marrow transplantationYoung Bae Sohn, Sung Won Park, Se-Hwa Kim, et al.
Annals of Clinical and Laboratory Science|August 17, 2011
Two novel PEX1 mutations in a patient with Zellweger syndrome: the first Korean case confirmed by biochemical, and molecular evidenceSung Yoon Cho, Young Pyo Chang, Ji Yun Park, et al.
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