Sohn YB - Search Results

1

Correction to: 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):369-370. doi: 10.1007/s12185-018-02590-x. Int J Hematol. 2019. PMID: 30632057

2

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

3

NF1 deficiency causes Bcl-xL upregulation in Schwann cells derived from neurofibromatosis type 1-associated malignant peripheral nerve sheath tumors.

Park HJ, Lee SJ, Sohn YB, Jin HS, Han JH, Kim YB, Yim H, Jeong SY. Park HJ, et al. Among authors: sohn yb. Int J Oncol. 2013 Feb;42(2):657-66. doi: 10.3892/ijo.2012.1751. Epub 2012 Dec 24. Int J Oncol. 2013. PMID: 23292448

4

The GBA p.G85E mutation in Korean patients with non-neuronopathic Gaucher disease: founder and neuroprotective effects.

Kim YM, Choi JH, Kim GH, Sohn YB, Ko JM, Lee BH, Cheon CK, Lim HH, Heo SH, Yoo HW. Kim YM, et al. Among authors: sohn yb. Orphanet J Rare Dis. 2020 Nov 11;15(1):318. doi: 10.1186/s13023-020-01597-0. Orphanet J Rare Dis. 2020. PMID: 33176831 Free PMC article.

5

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: sohn yb. 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.

6

Updates on Paget's Disease of Bone.

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.

7

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.

8

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.

9

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.

10

TAGLN expression is upregulated in NF1-associated malignant peripheral nerve sheath tumors by hypomethylation in its promoter and subpromoter regions.

Park GH, Lee SJ, Yim H, Han JH, Kim HJ, Sohn YB, Ko JM, Jeong SY. Park GH, et al. Among authors: sohn yb. Oncol Rep. 2014 Oct;32(4):1347-54. doi: 10.3892/or.2014.3379. Epub 2014 Aug 4. Oncol Rep. 2014. PMID: 25109740 Free PMC article.

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