Oh SH - Search Results

1

Severe form of neuroblastoma amplified sequence deficiency in an infant with recurrent acute liver failure.

Sunwoo Y, Kim YM, Kim EN, Oh SH, Lee BH. Sunwoo Y, et al. Among authors: oh sh. Pediatr Int. 2018 Mar;60(3):302-304. doi: 10.1111/ped.13476. Pediatr Int. 2018. PMID: 29575310 No abstract available.

2

Lack of common NOD2 mutations in Korean pediatric patients with inflammatory bowel disease.

Jang JY, Song SM, Kim KM, Oh SH, Lee YJ, Rhee KW. Jang JY, et al. Among authors: oh sh. Pediatr Int. 2010 Dec;52(6):888-9. doi: 10.1111/j.1442-200X.2010.03269.x. Pediatr Int. 2010. PMID: 21040192 No abstract available.

3

A Novel Frameshift Mutation of the ALDOB Gene in a Korean Girl Presenting with Recurrent Hepatitis Diagnosed as Hereditary Fructose Intolerance.

Choi HW, Lee YJ, Oh SH, Kim KM, Ryu JM, Lee BH, Kim GH, Yoo HW. Choi HW, et al. Among authors: oh sh. Gut Liver. 2012 Jan;6(1):126-8. doi: 10.5009/gnl.2012.6.1.126. Epub 2012 Jan 12. Gut Liver. 2012. PMID: 22375183 Free PMC article.

4

Differential clinical characteristics of acute liver failure caused by hemophagocytic lymphohistiocytosis in children.

Ryu JM, Kim KM, Oh SH, Koh KN, Im HJ, Park CJ, Chi HS, Seo JJ. Ryu JM, et al. Among authors: oh sh. Pediatr Int. 2013 Dec;55(6):748-52. doi: 10.1111/ped.12181. Epub 2013 Sep 18. Pediatr Int. 2013. PMID: 23848458

5

Improved outcomes in liver transplantation in children with acute liver failure.

Oh SH, Kim KM, Kim DY, Kim Y, Song SM, Lee YJ, Park SJ, Yoon CH, Ko GY, Sung KB, Hwang GS, Choi KT, Yu E, Song GW, Ha TY, Moon DB, Ahn CS, Kim KH, Hwang S, Park KM, Lee YJ, Lee SG. Oh SH, et al. J Pediatr Gastroenterol Nutr. 2014 Jan;58(1):68-73. doi: 10.1097/MPG.0b013e3182a80362. J Pediatr Gastroenterol Nutr. 2014. PMID: 23942007

6

Clinical features, outcomes, and genetic analysis in Korean children with Alagille syndrome.

Cho JM, Oh SH, Kim HJ, Kim JS, Kim KM, Kim GH, Yu E, Lee BH, Yoo HW. Cho JM, et al. Among authors: oh sh. Pediatr Int. 2015 Aug;57(4):552-7. doi: 10.1111/ped.12602. Epub 2015 May 6. Pediatr Int. 2015. PMID: 25676721

7

Diagnostic Value of Ceruloplasmin in the Diagnosis of Pediatric Wilson's Disease.

Kim JA, Kim HJ, Cho JM, Oh SH, Lee BH, Kim GH, Choi JH, Kim KM, Yoo HW. Kim JA, et al. Among authors: oh sh. Pediatr Gastroenterol Hepatol Nutr. 2015 Sep;18(3):187-92. doi: 10.5223/pghn.2015.18.3.187. Epub 2015 Sep 25. Pediatr Gastroenterol Hepatol Nutr. 2015. PMID: 26473139 Free PMC article.

8

Biochemical and molecular characteristics of citrin deficiency in Korean children.

Oh SH, Lee BH, Kim GH, Choi JH, Kim KM, Yoo HW. Oh SH, et al. J Hum Genet. 2017 Feb;62(2):305-307. doi: 10.1038/jhg.2016.131. Epub 2016 Nov 10. J Hum Genet. 2017. PMID: 27829683

9

Biochemical and molecular characterisation of neurological Wilson disease.

Seo GH, Kim YM, Oh SH, Chung SJ, Choi IH, Kim GH, Yum MS, Choi JH, Kim KM, Ko TS, Lee BH, Yoo HW. Seo GH, et al. Among authors: oh sh. J Med Genet. 2018 Sep;55(9):587-593. doi: 10.1136/jmedgenet-2017-105214. Epub 2018 Apr 4. J Med Genet. 2018. PMID: 29618506

10

Novel ATP8B1 Gene Mutations in a Child with Progressive Familial Intrahepatic Cholestasis Type 1.

Rhee ES, Kim YB, Lee S, Oh SH, Lee BH, Kim KM, Yoo HW. Rhee ES, et al. Among authors: oh sh. Pediatr Gastroenterol Hepatol Nutr. 2019 Sep;22(5):479-486. doi: 10.5223/pghn.2019.22.5.479. Epub 2019 Sep 11. Pediatr Gastroenterol Hepatol Nutr. 2019. PMID: 31555573 Free PMC article.

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