Sohn YB - Search Results

1

Choi YJ, Sohn YB, Chung YS. Choi YJ, et al. Among authors: sohn yb. Endocrinol Metab (Seoul). 2022 Oct;37(5):732-743. doi: 10.3803/EnM.2022.1575. Epub 2022 Oct 25. Endocrinol Metab (Seoul). 2022. PMID: 36327984 Free PMC article.

2

An unusual presentation of diabetic ketoacidosis in familial hajdu-cheney syndrome: a case report.

Lee GH, An SY, Sohn YB, Jeong SY, Chung YS. Lee GH, et al. Among authors: sohn yb. J Korean Med Sci. 2013 Nov;28(11):1682-6. doi: 10.3346/jkms.2013.28.11.1682. Epub 2013 Oct 31. J Korean Med Sci. 2013. PMID: 24265536 Free PMC article.

3

A Case of CATCH22 Syndrome Diagnosed in Postmenopausal Woman.

Lee SK, Lee MJ, Lee HJ, Kim BK, Sohn YB, Chung YS. Lee SK, et al. Among authors: sohn yb. J Bone Metab. 2013 May;20(1):57-60. doi: 10.11005/jbm.2013.20.1.57. Epub 2013 May 13. J Bone Metab. 2013. PMID: 24524058 Free PMC article.

4

A case report of pycnodysostosis with atypical femur fracture diagnosed by next-generation sequencing of candidate genes.

Song HK, Sohn YB, Choi YJ, Chung YS, Jang JH. Song HK, et al. Among authors: sohn yb. Medicine (Baltimore). 2017 Mar;96(12):e6367. doi: 10.1097/MD.0000000000006367. Medicine (Baltimore). 2017. PMID: 28328823 Free PMC article.

5

Using low-dose octreotide with diazoxide-resistant congenital hyperinsulinism resulting from compound heterozygous mutations in the ABCC8 gene.

Park K, Lim KI, Sohn YB, Lee HS, Hwang JS. Park K, et al. Among authors: sohn yb. Ann Pediatr Endocrinol Metab. 2023 Dec;28(Suppl 1):S23-S24. doi: 10.6065/apem.2244068.034. Epub 2022 Jun 29. Ann Pediatr Endocrinol Metab. 2023. PMID: 35798301 Free PMC article. No abstract available.

6

Genetic obesity: an update with emerging therapeutic approaches.

Sohn YB. Sohn YB. Ann Pediatr Endocrinol Metab. 2022 Sep;27(3):169-175. doi: 10.6065/apem.2244188.094. Epub 2022 Sep 30. Ann Pediatr Endocrinol Metab. 2022. PMID: 36203267 Free PMC article.

7

Improvement of cardiac function by short-term enzyme replacement therapy in a murine model of cardiomyopathy associated with Hunter syndrome evaluated by serial echocardiography with speckle tracking 2-D strain analysis.

Lee SC, Lee J, Jin DK, Kim JS, Jeon ES, Kwun YH, Chang MS, Ko AR, Yook YJ, Sohn YB. Lee SC, et al. Among authors: sohn yb. Mol Genet Metab. 2014 Jul;112(3):218-23. doi: 10.1016/j.ymgme.2014.04.005. Epub 2014 Apr 30. Mol Genet Metab. 2014. PMID: 24836711

8

AAV8-mediated expression of N-acetylglucosamine-1-phosphate transferase attenuates bone loss in a mouse model of mucolipidosis II.

Ko AR, Jin DK, Cho SY, Park SW, Przybylska M, Yew NS, Cheng SH, Kim JS, Kwak MJ, Kim SJ, Sohn YB. Ko AR, et al. Among authors: sohn yb. Mol Genet Metab. 2016 Apr;117(4):447-55. doi: 10.1016/j.ymgme.2016.02.001. Epub 2016 Feb 3. Mol Genet Metab. 2016. PMID: 26857995

9

Successful switching from insulin to sulfonylurea in a 3-month-old infant with diabetes due to p.G53D mutation in KCNJ11.

Yoon JS, Park KJ, Sohn YB, Lee HS, Hwang JS. Yoon JS, et al. Among authors: sohn yb. Ann Pediatr Endocrinol Metab. 2018 Sep;23(3):154-157. doi: 10.6065/apem.2018.23.3.154. Epub 2018 Sep 28. Ann Pediatr Endocrinol Metab. 2018. PMID: 30286572 Free PMC article.

10

Neuronopathic Gaucher disease presenting with microcytic hypochromic anemia.

Kim EA, Lim YT, Hah JO, Sohn YB, Kim YK, Choi JH, Kim SY, Jang KM, Ahn J, Lee JM. Kim EA, et al. Among authors: sohn yb. Int J Hematol. 2019 Mar;109(3):361-365. doi: 10.1007/s12185-018-2559-3. Epub 2018 Nov 19. Int J Hematol. 2019. PMID: 30456712

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