Kim DS - Search Results

1

Clinical pitfalls and serological diagnostics of MuSK myasthenia gravis.

Kwon YN, Woodhall M, Sung JJ, Kim KK, Lim YM, Kim H, Kim JE, Baek SH, Kim BJ, Park JS, Seok HY, Kim DS, Kwon O, Park KH, Sohn E, Bae JS, Yoon BN, Kim NH, Ahn SW, Choi K, Oh J, Park HJ, Shin KJ, Lee S, Park J, Kim SH, Seok JI, Bae DW, An JY, Joo IS, Choi SJ, Nam TS, Kim S, Park KJ, Kwon KH, Waters P, Hong YH. Kwon YN, et al. Among authors: kim ds, kim kk, kim h, kim sh, kim s, kim bj, kim nh, kim je. J Neurol. 2023 Mar;270(3):1478-1486. doi: 10.1007/s00415-022-11458-4. Epub 2022 Nov 17. J Neurol. 2023. PMID: 36396811 Free PMC article.

2

Long-term therapy with clevudine for chronic hepatitis B can be associated with myopathy characterized by depletion of mitochondrial DNA.

Seok JI, Lee DK, Lee CH, Park MS, Kim SY, Kim HS, Jo HY, Lee CH, Kim DS. Seok JI, et al. Among authors: kim ds, kim sy, kim hs. Hepatology. 2009 Jun;49(6):2080-6. doi: 10.1002/hep.22959. Hepatology. 2009. PMID: 19333909

3

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: kim ds, kim hs. 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.

4

Nemaline myopathy and non-fatal hypertrophic cardiomyopathy caused by a novel ACTA1 E239K mutation.

Kim SY, Park YE, Kim HS, Lee CH, Yang DH, Kim DS. Kim SY, et al. Among authors: kim ds, kim hs. J Neurol Sci. 2011 Aug 15;307(1-2):171-3. doi: 10.1016/j.jns.2011.04.022. Epub 2011 May 13. J Neurol Sci. 2011. PMID: 21570694

5

Exome sequencing identifies KIAA1377 and C5orf42 as susceptibility genes for monomelic amyotrophy.

Lim YM, Koh I, Park YM, Kim JJ, Kim DS, Kim HJ, Baik KH, Choi HY, Yang GS, Also-Rallo E, Tizzano EF, Gamez J, Park K, Yoo HW, Lee JK, Kim KK. Lim YM, et al. Among authors: kim ds, kim jj, kim kk, kim hj. Neuromuscul Disord. 2012 May;22(5):394-400. doi: 10.1016/j.nmd.2011.11.006. Epub 2012 Jan 20. Neuromuscul Disord. 2012. PMID: 22264561

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: kim ds, kim hs. 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

Comparison between clinical disabilities and electrophysiological values in Charcot-Marie-Tooth 1A patients with PMP22 duplication.

Kim YH, Chung HK, Park KD, Choi KG, Kim SM, Sunwoo IN, Choi YC, Lim JG, Lee KW, Kim KK, Lee DK, Joo IS, Kwon KH, Gwon SB, Park JH, Kim DS, Kim SH, Kim WK, Suh BC, Kim SB, Kim NH, Sohn EH, Kim OJ, Kim HS, Cho JH, Kang SY, Park CI, Oh J, Shin JH, Chung KW, Choi BO. Kim YH, et al. Among authors: kim ds, kim sb, kim kk, kim wk, kim sh, kim sm, kim nh, kim oj, kim hs. J Clin Neurol. 2012 Jun;8(2):139-45. doi: 10.3988/jcn.2012.8.2.139. Epub 2012 Jun 29. J Clin Neurol. 2012. PMID: 22787498 Free PMC article.

8

Limb-girdle phenotype is frequent in patients with myopathy associated with GNE mutations.

Park YE, Kim HS, Choi ES, Shin JH, Kim SY, Son EH, Lee CH, Kim DS. Park YE, et al. Among authors: kim ds, kim sy, kim hs. J Neurol Sci. 2012 Oct 15;321(1-2):77-81. doi: 10.1016/j.jns.2012.07.061. Epub 2012 Aug 9. J Neurol Sci. 2012. PMID: 22883483

9

Autonomic dysfunction in SCN9A-associated primary erythromelalgia.

Kim MK, Yuk JW, Kim HS, Park KJ, Kim DS. Kim MK, et al. Among authors: kim ds, kim hs. Clin Auton Res. 2013 Apr;23(2):105-7. doi: 10.1007/s10286-012-0181-7. Epub 2012 Nov 15. Clin Auton Res. 2013. PMID: 23152140

10

A recurrent longitudinally extensive transverse myelitis with Aquaporin-4(AQP4) antibody after herpes zoster.

Park JS, Hwang SJ, Shin JH, Kim DS. Park JS, et al. Among authors: kim ds. J Neurol Sci. 2013 Nov 15;334(1-2):69-71. doi: 10.1016/j.jns.2013.07.2510. Epub 2013 Jul 31. J Neurol Sci. 2013. PMID: 23953947

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