Ko JS - Search Results

1

Hereditary Fructose Intolerance Diagnosed in Adulthood.

Kim MS, Moon JS, Kim MJ, Seong MW, Park SS, Ko JS. Kim MS, et al. Among authors: ko js. Gut Liver. 2021 Jan 15;15(1):142-145. doi: 10.5009/gnl20189. Gut Liver. 2021. PMID: 33028743 Free PMC article.

2

Neonatal intrahepatic cholestasis caused by citrin deficiency in Korean infants.

Ko JS, Song JH, Park SS, Seo JK. Ko JS, et al. J Korean Med Sci. 2007 Dec;22(6):952-6. doi: 10.3346/jkms.2007.22.6.952. J Korean Med Sci. 2007. PMID: 18162705 Free PMC article.

3

Tufting Enteropathy with EpCAM Mutations in Two Siblings.

Ko JS, Seo JK, Shim JO, Hwang SH, Park HS, Kang GH. Ko JS, et al. Gut Liver. 2010 Sep;4(3):407-10. doi: 10.5009/gnl.2010.4.3.407. Epub 2010 Sep 24. Gut Liver. 2010. PMID: 20981223 Free PMC article.

4

Changes in pulmonary artery pressures during ethanol sclerotherapy for arteriovenous malformations: identifying the most vulnerable period.

Ko JS, Kim CS, Shin BS, Kim MJ, Lee JH, Kim KH, Do YS. Ko JS, et al. Clin Radiol. 2011 Jul;66(7):639-44. doi: 10.1016/j.crad.2011.03.003. Epub 2011 Apr 21. Clin Radiol. 2011. PMID: 21513926

5

Impedance-pH monitoring and conventional pH monitoring are complementary methods to detect association between gastroesophageal reflux and apnea-related symptoms in preterm infants and neonates.

Shin MS, Shim JO, Moon JS, Kim HS, Ko JS, Choi JH, Seo JK. Shin MS, et al. Among authors: ko js. J Matern Fetal Neonatal Med. 2012 Nov;25(11):2406-10. doi: 10.3109/14767058.2012.697944. Epub 2012 Jun 25. J Matern Fetal Neonatal Med. 2012. PMID: 22694343

6

Interleukin-10 receptor mutations in children with neonatal-onset Crohn's disease and intractable ulcerating enterocolitis.

Shim JO, Hwang S, Yang HR, Moon JS, Chang JY, Ko JS, Park SS, Kang GH, Kim WS, Seo JK. Shim JO, et al. Among authors: ko js. Eur J Gastroenterol Hepatol. 2013 Oct;25(10):1235-40. doi: 10.1097/MEG.0b013e328361a4f9. Eur J Gastroenterol Hepatol. 2013. PMID: 23839161

7

A mutation analysis of the AGL gene in Korean patients with glycogen storage disease type III.

Ko JS, Moon JS, Seo JK, Yang HR, Chang JY, Park SS. Ko JS, et al. J Hum Genet. 2014 Jan;59(1):42-5. doi: 10.1038/jhg.2013.117. Epub 2013 Nov 21. J Hum Genet. 2014. PMID: 24257475

8

Molecular Analysis of the UGT1A1 Gene in Korean Patients with Crigler-Najjar Syndrome Type II.

Ko JS, Chang JY, Moon JS, Yang HR, Seo JK. Ko JS, et al. Pediatr Gastroenterol Hepatol Nutr. 2014 Mar;17(1):37-40. doi: 10.5223/pghn.2014.17.1.37. Epub 2014 Mar 31. Pediatr Gastroenterol Hepatol Nutr. 2014. PMID: 24749086 Free PMC article.

9

Epstein-barr virus infection with acute acalculous cholecystitis.

Kim A, Yang HR, Moon JS, Chang JY, Ko JS. Kim A, et al. Among authors: ko js. Pediatr Gastroenterol Hepatol Nutr. 2014 Mar;17(1):57-60. doi: 10.5223/pghn.2014.17.1.57. Epub 2014 Mar 31. Pediatr Gastroenterol Hepatol Nutr. 2014. PMID: 24749090 Free PMC article.

10

Identification of novel mutations in the VPS33B gene involved in arthrogryposis, renal dysfunction, and cholestasis syndrome.

Seo SH, Hwang SM, Ko JM, Ko JS, Hyun YJ, Cho SI, Park H, Kim SY, Seong MW, Park SS. Seo SH, et al. Among authors: ko js, ko jm. Clin Genet. 2015 Jul;88(1):80-4. doi: 10.1111/cge.12442. Epub 2014 Aug 7. Clin Genet. 2015. PMID: 24917129

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