Nam SO - Search Results

1

Diagnostic mutational analysis of MECP2 in Korean patients with Rett syndrome.

Kim IJ, Kim YJ, Son BH, Nam SO, Kang HC, Kim HD, Yoo MA, Choi OH, Kim CM. Kim IJ, et al. Among authors: nam so. Exp Mol Med. 2006 Apr 30;38(2):119-25. doi: 10.1038/emm.2006.15. Exp Mol Med. 2006. PMID: 16672765 Free article.

2

Epilepsy-related clinical factors and psychosocial functions in pediatric epilepsy.

Eom S, Eun SH, Kang HC, Eun BL, Nam SO, Kim SJ, Chung HJ, Kwon SH, Lee YM, Lee JS, Kim DW, Oh KJ, Kim HD. Eom S, et al. Among authors: nam so. Epilepsy Behav. 2014 Aug;37:43-8. doi: 10.1016/j.yebeh.2014.05.019. Epub 2014 Jun 25. Epilepsy Behav. 2014. PMID: 24972158

3

Perceived stigma in Korean adolescents with epilepsy: Effects of knowledge about epilepsy and maternal perception of stigma.

Ryu HU, Lee SA, Eom S, Kim HD; Korean QoL in Epilepsy Study Group. Ryu HU, et al. Seizure. 2015 Jan;24:38-43. doi: 10.1016/j.seizure.2014.11.010. Epub 2014 Dec 3. Seizure. 2015. PMID: 25564318 Free article.

4

Neuropsychological effects of levetiracetam and carbamazepine in children with focal epilepsy.

Jung DE, Yu R, Yoon JR, Eun BL, Kwon SH, Lee YJ, Eun SH, Lee JS, Kim HD, Nam SO, Kim GH, Hwang SK, Eom S, Kang DR, Kang HC. Jung DE, et al. Among authors: nam so. Neurology. 2015 Jun 9;84(23):2312-9. doi: 10.1212/WNL.0000000000001661. Epub 2015 May 6. Neurology. 2015. PMID: 25948717 Clinical Trial.

5

A Unique Mutational Spectrum of MLC1 in Korean Patients With Megalencephalic Leukoencephalopathy With Subcortical Cysts: p.Ala275Asp Founder Mutation and Maternal Uniparental Disomy of Chromosome 22.

Choi SA, Kim SY, Yoon J, Choi J, Park SS, Seong MW, Kim H, Hwang H, Choi JE, Chae JH, Kim KJ, Kim S, Lee YJ, Nam SO, Lim BC. Choi SA, et al. Among authors: nam so. Ann Lab Med. 2017 Nov;37(6):516-521. doi: 10.3343/alm.2017.37.6.516. Ann Lab Med. 2017. PMID: 28840990 Free PMC article.

6

Clinical characterization of anti-GQ1b antibody syndrome in Korean children.

Yoon L, Kim BR, Kim HY, Kwak MJ, Park KH, Bae MH, Lee Y, Nam SO, Choi HY, Kim YM. Yoon L, et al. Among authors: nam so. J Neuroimmunol. 2019 May 15;330:170-173. doi: 10.1016/j.jneuroim.2019.01.003. Epub 2019 Jan 8. J Neuroimmunol. 2019. PMID: 30642576

7

Myelin oligodendrocyte glycoprotein antibody-associated disorders: clinical spectrum, diagnostic evaluation, and treatment options.

Lee YJ, Nam SO, Ko A, Kong J, Byun SY. Lee YJ, et al. Among authors: nam so. Clin Exp Pediatr. 2021 Mar;64(3):103-110. doi: 10.3345/cep.2019.01305. Epub 2020 May 14. Clin Exp Pediatr. 2021. PMID: 32403899 Free PMC article.

8

Characteristics of Genetic Variations Associated With Lennox-Gastaut Syndrome in Korean Families.

Yang JO, Choi MH, Yoon JY, Lee JJ, Nam SO, Jun SY, Kwon HH, Yun S, Jeon SJ, Byeon I, Halder D, Kong J, Lee B, Lee J, Kang JW, Kim NS. Yang JO, et al. Among authors: nam so. Front Genet. 2021 Jan 20;11:590924. doi: 10.3389/fgene.2020.590924. eCollection 2020. Front Genet. 2021. PMID: 33584793 Free PMC article.

9

Hemophagocytic syndrome associated with Kikuchi's disease.

Kim YM, Lee YJ, Nam SO, Park SE, Kim JY, Lee EY. Kim YM, et al. Among authors: nam so. J Korean Med Sci. 2003 Aug;18(4):592-4. doi: 10.3346/jkms.2003.18.4.592. J Korean Med Sci. 2003. PMID: 12923340 Free PMC article.

10

Optic Neuritis in Korean Children: Low Risk of Subsequent Multiple Sclerosis.

Kim YM, Kim HY, Cho MJ, Kwak MJ, Park KH, Yeon GM, Lee Y, Nam SO. Kim YM, et al. Among authors: nam so. Pediatr Neurol. 2015 Sep;53(3):221-5. doi: 10.1016/j.pediatrneurol.2015.05.010. Epub 2015 May 29. Pediatr Neurol. 2015. PMID: 26183177

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