Choi YC - Search Results

1

Nogo-A Is Critical for Pro-Inflammatory Gene Regulation in Myocytes and Macrophages.

Ullah HMA, Elfadl AK, Park S, Kim YD, Chung MJ, Son JY, Yun HH, Park JM, Yim JH, Jung SJ, Choi YC, Shin JH, Kim DS, Park JK, Jeong KS. Ullah HMA, et al. Among authors: choi yc. Cells. 2021 Jan 31;10(2):282. doi: 10.3390/cells10020282. Cells. 2021. PMID: 33572505 Free PMC article.

2

Phenotypic variability in Kennedy's disease: implication of the early diagnostic features.

Lee JH, Shin JH, Park KP, Kim IJ, Kim CM, Lim JG, Choi YC, Kim DS. Lee JH, et al. Among authors: choi yc. Acta Neurol Scand. 2005 Jul;112(1):57-63. doi: 10.1111/j.1600-0404.2005.00428.x. Acta Neurol Scand. 2005. PMID: 15932358

3

CCR2-64I and CCR5Delta32 Polymorphisms in Korean Patients with Myasthenia Gravis.

Kim HS, Kim DS, Lee EY, Sunwoo IN, Choi YC. Kim HS, et al. Among authors: choi yc. J Clin Neurol. 2007 Sep;3(3):133-8. doi: 10.3988/jcn.2007.3.3.133. Epub 2007 Sep 20. J Clin Neurol. 2007. PMID: 19513280 Free PMC article.

4

Novel CLCN1 mutations and clinical features of Korean patients with myotonia congenita.

Moon IS, Kim HS, Shin JH, Park YE, Park KH, Shin YB, Bae JS, Choi YC, Kim DS. Moon IS, et al. Among authors: choi yc. J Korean Med Sci. 2009 Dec;24(6):1038-44. doi: 10.3346/jkms.2009.24.6.1038. Epub 2009 Nov 9. J Korean Med Sci. 2009. PMID: 19949657 Free PMC article.

5

Clinical Diversity of SCN4A-Mutation-Associated Skeletal Muscle Sodium Channelopathy.

Lee SC, Kim HS, Park YE, Choi YC, Park KH, Kim DS. Lee SC, et al. Among authors: choi yc. J Clin Neurol. 2009 Dec;5(4):186-91. doi: 10.3988/jcn.2009.5.4.186. Epub 2009 Dec 31. J Clin Neurol. 2009. PMID: 20076800 Free PMC article.

6

Two common mutations (p.Gln832X and c.663+1G>C) account for about a third of the DYSF mutations in Korean patients with dysferlinopathy.

Park YE, Kim HS, Lee CH, Nam TS, Choi YC, Kim DS. Park YE, et al. Among authors: choi yc. Neuromuscul Disord. 2012 Jun;22(6):505-10. doi: 10.1016/j.nmd.2011.12.007. Epub 2012 Jan 31. Neuromuscul Disord. 2012. PMID: 22297152

7

Clinical and Pathological Features of Korean Patients with DNM2-Related Centronuclear Myopathy.

Park YE, Choi YC, Bae JS, Lee CH, Kim HS, Shin JH, Kim DS. Park YE, et al. Among authors: choi yc. J Clin Neurol. 2014 Jan;10(1):24-31. doi: 10.3988/jcn.2014.10.1.24. Epub 2014 Jan 6. J Clin Neurol. 2014. PMID: 24465259 Free PMC article.

8

Whole-genome analysis in Korean patients with autoimmune myasthenia gravis.

Na SJ, Lee JH, Kim SW, Kim DS, Shon EH, Park HJ, Shin HY, Kim SM, Choi YC. Na SJ, et al. Among authors: choi yc. Yonsei Med J. 2014 May;55(3):660-8. doi: 10.3349/ymj.2014.55.3.660. Epub 2014 Apr 1. Yonsei Med J. 2014. PMID: 24719132 Free PMC article.

9

Effect of enzyme replacement therapy in late onset Pompe disease: open pilot study of 48 weeks follow-up.

Park JS, Kim HG, Shin JH, Choi YC, Kim DS. Park JS, et al. Among authors: choi yc. Neurol Sci. 2015 Apr;36(4):599-605. doi: 10.1007/s10072-014-2000-5. Epub 2014 Nov 12. Neurol Sci. 2015. PMID: 25388776

10

Targeted population screening of late onset Pompe disease in unspecified myopathy patients for Korean population.

Lee JH, Shin JH, Park HJ, Kim SZ, Jeon YM, Kim HK, Kim DS, Choi YC. Lee JH, et al. Among authors: choi yc. Neuromuscul Disord. 2017 Jun;27(6):550-556. doi: 10.1016/j.nmd.2017.03.005. Epub 2017 Mar 10. Neuromuscul Disord. 2017. PMID: 28433475

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