Kim DS - Search Results

1

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.

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: kim ds, kim ij, kim cm. 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

A novel PYGM mutation in a Korean patient with McArdle disease: the role of nonsense-mediated mRNA decay.

Sohn EH, Kim HS, Lee AY, Fukuda T, Sugie H, Kim DS. Sohn EH, et al. Among authors: kim ds, kim hs. Neuromuscul Disord. 2008 Nov;18(11):886-9. doi: 10.1016/j.nmd.2008.06.384. Epub 2008 Jul 29. Neuromuscul Disord. 2008. PMID: 18667317

4

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: kim ds. 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.

5

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.

6

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: kim ds, kim hs. 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.

7

SLC25A4 and C10ORF2 Mutations in Autosomal Dominant Progressive External Ophthalmoplegia.

Park KP, Kim HS, Kim ES, Park YE, Lee CH, Kim DS. Park KP, et al. Among authors: kim ds, kim hs, kim es. J Clin Neurol. 2011 Mar;7(1):25-30. doi: 10.3988/jcn.2011.7.1.25. Epub 2011 Mar 31. J Clin Neurol. 2011. PMID: 21519523 Free PMC article.

8

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

9

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: kim ds, kim hs. 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.

10

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: kim ds, kim sw, kim sm. 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.

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