Han SJ - Search Results

1

A study of the relationship between clinical phenotypes and plasma iduronate-2-sulfatase enzyme activities in Hunter syndrome patients.

Lee OJ, Kim SJ, Sohn YB, Park HD, Lee SY, Kim CH, Ko AR, Yook YJ, Lee SJ, Park SW, Kim SH, Cho SY, Kwon EK, Han SJ, Jin DK. Lee OJ, et al. Among authors: han sj. Korean J Pediatr. 2012 Mar;55(3):88-92. doi: 10.3345/kjp.2012.55.3.88. Epub 2012 Mar 16. Korean J Pediatr. 2012. PMID: 22474463 Free PMC article.

2

Clinical and molecular characterization of Korean children with infantile and late-onset Pompe disease: 10 years of experience with enzyme replacement therapy at a single center.

Kim MS, Song A, Im M, Huh J, Kang IS, Song J, Yang A, Kim J, Kwon EK, Choi EJ, Han SJ, Park HD, Cho SY, Jin DK. Kim MS, et al. Among authors: han sj. Korean J Pediatr. 2019 Jun;62(6):224-234. doi: 10.3345/kjp.2018.06968. Epub 2018 Oct 4. Korean J Pediatr. 2019. PMID: 30360039 Free PMC article.

3

Impact of enzyme replacement therapy on linear growth in Korean patients with mucopolysaccharidosis type II (Hunter syndrome).

Cho SY, Huh R, Chang MS, Lee J, Kwun Y, Maeng SH, Kim SJ, Sohn YB, Park SW, Kwon EK, Han SJ, Jung J, Jin DK. Cho SY, et al. Among authors: han sj. J Korean Med Sci. 2014 Feb;29(2):254-60. doi: 10.3346/jkms.2014.29.2.254. Epub 2014 Jan 28. J Korean Med Sci. 2014. PMID: 24550654 Free PMC article.

4

Phase I/II clinical trial of enzyme replacement therapy with idursulfase beta in patients with mucopolysaccharidosis II (Hunter syndrome).

Sohn YB, Cho SY, Park SW, Kim SJ, Ko AR, Kwon EK, Han SJ, Jin DK. Sohn YB, et al. Among authors: han sj. Orphanet J Rare Dis. 2013 Mar 18;8:42. doi: 10.1186/1750-1172-8-42. Orphanet J Rare Dis. 2013. PMID: 23497636 Free PMC article. Clinical Trial.

5

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 transplantation.

Sohn YB, Park SW, Kim SH, Cho SY, Ji ST, Kwon EK, Han SJ, Oh SJ, Park YJ, Ko AR, Paik KH, Lee J, Lee DH, Jin DK. Sohn YB, et al. Among authors: han sj. Am J Med Genet A. 2012 May;158A(5):1158-63. doi: 10.1002/ajmg.a.35263. Epub 2012 Apr 11. Am J Med Genet A. 2012. PMID: 22495825

6

Suppression of acylated ghrelin during oral glucose tolerance test is correlated with whole-body insulin sensitivity in children with Prader-Willi syndrome.

Paik KH, Choe YH, Park WH, Oh YJ, Kim AH, Chu SH, Kim SW, Kwon EK, Han SJ, Shon WY, Jin DK. Paik KH, et al. Among authors: han sj. J Clin Endocrinol Metab. 2006 May;91(5):1876-81. doi: 10.1210/jc.2005-2168. Epub 2006 Feb 28. J Clin Endocrinol Metab. 2006. PMID: 16507634

7

Obestatin is not elevated or correlated with insulin in children with Prader-Willi syndrome.

Park WH, Oh YJ, Kim GY, Kim SE, Paik KH, Han SJ, Kim AH, Chu SH, Kwon EK, Kim SW, Jin DK. Park WH, et al. Among authors: han sj. J Clin Endocrinol Metab. 2007 Jan;92(1):229-34. doi: 10.1210/jc.2006-0754. Epub 2006 Oct 17. J Clin Endocrinol Metab. 2007. PMID: 17047025

8

Development and validation of the Pediatric-Youth Hyperphagia Assessment for Prader-Willi syndrome.

Cho SY, Kang D, Im M, Yang A, Kim MS, Kim J, Noh ES, Kwon EK, Choi E, Han S, Park YA, Kwak MJ, Kim Y, Cho J, Jin DK. Cho SY, et al. Epidemiol Health. 2022;44:e2022014. doi: 10.4178/epih.e2022014. Epub 2022 Jan 10. Epidemiol Health. 2022. PMID: 35038830 Free PMC article.

9

Next-generation Sequencing of MicroRNA in Acquired Middle Ear Cholesteatoma.

Han SJ, Kim SK, Hong SM. Han SJ, et al. Laryngoscope. 2024 May 22. doi: 10.1002/lary.31507. Online ahead of print. Laryngoscope. 2024. PMID: 38775212

10

N-Myc and STAT Interactor is an endometriosis suppressor.

Park Y, Guan X, Han SJ. Park Y, et al. Among authors: han sj. bioRxiv [Preprint]. 2024 May 10:2024.05.08.593227. doi: 10.1101/2024.05.08.593227. bioRxiv. 2024. PMID: 38766020 Free PMC article. Preprint.

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