Heo SH - Search Results

1

The early molecular processes underlying the neurological manifestations of an animal model of Wilson's disease.

Lee BH, Kim JH, Kim JM, Heo SH, Kang M, Kim GH, Choi JH, Yoo HW. Lee BH, et al. Among authors: heo sh. Metallomics. 2013 May;5(5):532-40. doi: 10.1039/c3mt20243g. Epub 2013 Mar 21. Metallomics. 2013. PMID: 23519153

2

Mutations of the GLA gene in Korean patients with Fabry disease and frequency of the E66Q allele as a functional variant in Korean newborns.

Lee BH, Heo SH, Kim GH, Park JY, Kim WS, Kang DH, Choe KH, Kim WH, Yang SH, Yoo HW. Lee BH, et al. Among authors: heo sh. J Hum Genet. 2010 Aug;55(8):512-7. doi: 10.1038/jhg.2010.58. Epub 2010 May 27. J Hum Genet. 2010. PMID: 20505683

3

Proteomic analysis of sera of asymptomatic, early-stage patients with Wilson's disease.

Park JY, Mun JH, Lee BH, Heo SH, Kim GH, Yoo HW. Park JY, et al. Among authors: heo sh. Proteomics Clin Appl. 2009 Oct;3(10):1185-1190. doi: 10.1002/prca.200800057. Proteomics Clin Appl. 2009. PMID: 20556197 Free PMC article.

4

Proteomic analysis of the hepatic tissue of Long-Evans Cinnamon (LEC) rats according to the natural course of Wilson disease.

Lee BH, Kim JM, Heo SH, Mun JH, Kim J, Kim JH, Jin HY, Kim GH, Choi JH, Yoo HW. Lee BH, et al. Among authors: heo sh. Proteomics. 2011 Sep;11(18):3698-705. doi: 10.1002/pmic.201100122. Epub 2011 Aug 9. Proteomics. 2011. PMID: 21751376

5

High prevalence of neonatal presentation in Korean patients with citrullinemia type 1, and their shared mutations.

Lee BH, Kim YM, Heo SH, Kim GH, Choi IH, Lee BS, Kim EA, Kim KS, Jhang WK, Park SJ, Yoo HW. Lee BH, et al. Among authors: heo sh. Mol Genet Metab. 2013 Jan;108(1):18-24. doi: 10.1016/j.ymgme.2012.11.011. Epub 2012 Nov 28. Mol Genet Metab. 2013. PMID: 23246278

6

Comparative proteomic analysis in children with idiopathic short stature (ISS) before and after short-term recombinant human growth hormone (rhGH) therapy.

Heo SH, Choi JH, Kim YM, Jung CW, Lee J, Jin HY, Kim GH, Lee BH, Shin CH, Yoo HW. Heo SH, et al. Proteomics. 2013 Apr;13(7):1211-9. doi: 10.1002/pmic.201200131. Epub 2013 Mar 4. Proteomics. 2013. PMID: 23436750 Clinical Trial.

7

Allele frequency of a 24 bp duplication in exon 10 of the CHIT1 gene in the general Korean population and in Korean patients with Gaucher disease.

Woo KH, Lee BH, Heo SH, Kim JM, Kim GH, Kim YM, Kim JH, Choi IH, Yang SH, Yoo HW. Woo KH, et al. Among authors: heo sh. J Hum Genet. 2014 May;59(5):276-9. doi: 10.1038/jhg.2014.16. Epub 2014 Mar 13. J Hum Genet. 2014. PMID: 24621582

8

High frequency of DUOX2 mutations in transient or permanent congenital hypothyroidism with eutopic thyroid glands.

Jin HY, Heo SH, Kim YM, Kim GH, Choi JH, Lee BH, Yoo HW. Jin HY, et al. Among authors: heo sh. Horm Res Paediatr. 2014;82(4):252-60. doi: 10.1159/000362235. Epub 2014 Sep 20. Horm Res Paediatr. 2014. PMID: 25248169

9

A phase 2 multi-center, open-label, switch-over trial to evaluate the safety and efficacy of Abcertin® in patients with type 1 Gaucher disease.

Choi JH, Lee BH, Ko JM, Sohn YB, Lee JS, Kim GH, Heo SH, Park JY, Kim YM, Kim JH, Yoo HW. Choi JH, et al. Among authors: heo sh. J Korean Med Sci. 2015 Apr;30(4):378-84. doi: 10.3346/jkms.2015.30.4.378. Epub 2015 Mar 19. J Korean Med Sci. 2015. PMID: 25829804 Free PMC article. Clinical Trial.

10

Erratum: A Phase 2 Multi-center, Open-label, Switch-over Trial to Evaluate the Safety and Efficacy of Abcertin® in Patients with Type 1 Gaucher Disease.

Choi JH, Lee BH, Ko JM, Sohn YB, Lee JS, Kim GH, Heo SH, Park JY, Kim YM, Kim JH, Yoo HW. Choi JH, et al. Among authors: heo sh. J Korean Med Sci. 2015 Sep;30(9):1373. doi: 10.3346/jkms.2015.30.9.1373. J Korean Med Sci. 2015. PMID: 26339182 Free PMC article. No abstract available.

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