Kim DS - Search Results

1

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.

2

Histochemical and molecular genetic study of MELAS and MERRF in Korean patients.

Kim DS, Jung DS, Park KH, Kim IJ, Kim CM, Lee WH, Rho SK. Kim DS, et al. Among authors: kim ij, kim cm. J Korean Med Sci. 2002 Feb;17(1):103-12. doi: 10.3346/jkms.2002.17.1.103. J Korean Med Sci. 2002. PMID: 11850598 Free PMC article.

3

A Korean family with Arg1448Cys mutation of SCN4A channel causing paramyotonia congenita: electrophysiologic, histopathologic, and molecular genetic studies.

Kim DS, Kim EJ, Jung DS, Park KH, Kim IJ, Kwak KY, Kim CM, Ko HY. Kim DS, et al. Among authors: kim ij, kim ej, kim cm. J Korean Med Sci. 2002 Dec;17(6):856-60. doi: 10.3346/jkms.2002.17.6.856. J Korean Med Sci. 2002. PMID: 12483017 Free PMC article.

4

A case of Lambert-Eaton myasthenic syndrome associated with atypical bronchopulmonary carcinoid tumor.

Lee JH, Shin JH, Kim DS, Jung DS, Park KH, Lee MK, Kim JY. Lee JH, et al. Among authors: kim ds, kim jy. J Korean Med Sci. 2004 Oct;19(5):753-5. doi: 10.3346/jkms.2004.19.5.753. J Korean Med Sci. 2004. PMID: 15483357 Free PMC article.

5

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

6

Hemispheric asymmetry of median nerve somatosensory evoked potentials.

Park KH, Kim DS, Park BK. Park KH, et al. Among authors: kim ds. Suppl Clin Neurophysiol. 2006;59:233-8. doi: 10.1016/s1567-424x(09)70036-4. Suppl Clin Neurophysiol. 2006. PMID: 16893117 No abstract available.

7

Two new missense mutations of GAA in late onset glycogen storage disease type II.

Park YE, Park KH, Lee CH, Kim CM, Kim DS. Park YE, et al. Among authors: kim ds, kim cm. J Neurol Sci. 2006 Dec 21;251(1-2):113-7. doi: 10.1016/j.jns.2006.09.012. Epub 2006 Nov 7. J Neurol Sci. 2006. PMID: 17092519

8

Mutations of CAPN3 in Korean patients with limb-girdle muscular dystrophy.

Shin JH, Kim HS, Lee CH, Kim CM, Park KH, Kim DS. Shin JH, et al. Among authors: kim ds, kim cm, kim hs. J Korean Med Sci. 2007 Jun;22(3):463-9. doi: 10.3346/jkms.2007.22.3.463. J Korean Med Sci. 2007. PMID: 17596655 Free PMC article.

9

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

10

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

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