Kim SH - Search Results

1

Clinical and genetic analysis of MAPT, GRN, and C9orf72 genes in Korean patients with frontotemporal dementia.

Kim EJ, Kwon JC, Park KH, Park KW, Lee JH, Choi SH, Jeong JH, Kim BC, Yoon SJ, Yoon YC, Kim S, Park KC, Choi BO, Na DL, Ki CS, Kim SH. Kim EJ, et al. Among authors: kim bc, kim sh, kim s. Neurobiol Aging. 2014 May;35(5):1213.e13-7. doi: 10.1016/j.neurobiolaging.2013.11.033. Epub 2013 Dec 4. Neurobiol Aging. 2014. PMID: 24387985

2

Mutation analysis of the GNE gene in Korean patients with distal myopathy with rimmed vacuoles.

Kim BJ, Ki CS, Kim JW, Sung DH, Choi YC, Kim SH. Kim BJ, et al. Among authors: kim sh, kim jw. J Hum Genet. 2006;51(2):137-140. doi: 10.1007/s10038-005-0338-5. Epub 2005 Dec 22. J Hum Genet. 2006. PMID: 16372135

3

Clinical characteristics of familial amyotrophic lateral sclerosis with a Phe20Cys mutation in the SOD1 gene in a Korean family.

Kim HY, Ki CS, Koh SH, Park KH, Sunwoo IN, Kim SH. Kim HY, et al. Among authors: kim sh. Amyotroph Lateral Scler. 2007 Apr;8(2):73-8. doi: 10.1080/17482960701223154. Amyotroph Lateral Scler. 2007. PMID: 17453632

4

Prognosis of ocular myasthenia in Korea: a retrospective multicenter analysis of 202 patients.

Hong YH, Kwon SB, Kim BJ, Kim BJ, Kim SH, Kim JK, Park KS, Park KJ, Sung JJ, Sohn EH, Lee YB, Jeong D, Joo IS, Choi BO, Choi YC; Korean Research Group for Neuromuscular Diseases. Hong YH, et al. Among authors: kim jk, kim sh, kim bj. J Neurol Sci. 2008 Oct 15;273(1-2):10-4. doi: 10.1016/j.jns.2008.05.023. Epub 2008 Jul 3. J Neurol Sci. 2008. PMID: 18602121

5

A novel LMNA gene mutation Leu162Pro and the associated clinical characteristics in a family with autosomal-dominant emery-dreifuss muscular dystrophy.

Kim HY, Ki CS, Kang SJ, Khang SK, Koh SH, Kim DW, Kim SH, Sung IH. Kim HY, et al. Among authors: kim dw, kim sh. Muscle Nerve. 2008 Oct;38(4):1336-9. doi: 10.1002/mus.21066. Muscle Nerve. 2008. PMID: 18816602

6

Cilnidipine mediates a neuroprotective effect by scavenging free radicals and activating the phosphatidylinositol 3-kinase pathway.

Lee YJ, Park KH, Park HH, Kim YJ, Lee KY, Kim SH, Koh SH. Lee YJ, et al. Among authors: kim yj, kim sh. J Neurochem. 2009 Oct;111(1):90-100. doi: 10.1111/j.1471-4159.2009.06297.x. Epub 2009 Jul 23. J Neurochem. 2009. PMID: 19650875 Free article.

7

Presenilin 1 gene mutation (M139I) in a patient with an early-onset Alzheimer's disease: clinical characteristics and genetic identification.

Kim HJ, Kim HY, Ki CS, Kim SH. Kim HJ, et al. Among authors: kim hy, kim sh. Neurol Sci. 2010 Dec;31(6):781-3. doi: 10.1007/s10072-010-0233-5. Epub 2010 Mar 6. Neurol Sci. 2010. PMID: 20213228

8

A novel codon4 mutation (A4F) in the SOD1gene in familial amyotrophic lateral sclerosis.

Baek W, Koh SH, Park JS, Kim YS, Kim HY, Kwon MJ, Ki CS, Kim SH. Baek W, et al. Among authors: kim hy, kim sh, kim ys. J Neurol Sci. 2011 Jul 15;306(1-2):157-9. doi: 10.1016/j.jns.2011.03.041. Epub 2011 Apr 14. J Neurol Sci. 2011. PMID: 21496827

9

Screening of the SOD1, FUS, TARDBP, ANG, and OPTN mutations in Korean patients with familial and sporadic ALS.

Kwon MJ, Baek W, Ki CS, Kim HY, Koh SH, Kim JW, Kim SH. Kwon MJ, et al. Among authors: kim hy, kim sh, kim jw. Neurobiol Aging. 2012 May;33(5):1017.e17-23. doi: 10.1016/j.neurobiolaging.2011.12.003. Epub 2012 Jan 15. Neurobiol Aging. 2012. PMID: 22244934

10

A novel exon 3 mutation (P66S) in the SOD1 gene in familial ALS.

Baek W, Koh SH, Kim YS, Kim HY, Kwon MJ, Ki CS, Kim SH. Baek W, et al. Among authors: kim hy, kim sh, kim ys. Can J Neurol Sci. 2012 Mar;39(2):245-6. doi: 10.1017/s0317167100013329. Can J Neurol Sci. 2012. PMID: 22343163 No abstract available.

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