Park SS - Search Results

1

Investigation of the association between normal-tension glaucoma and single nucleotide polymorphisms in natriuretic peptide gene.

Jeoung JW, Kim DM, Ko HS, Park SS, Kim JY, Kim SY, Yoo TW. Jeoung JW, et al. Among authors: park ss. Korean J Ophthalmol. 2007 Mar;21(1):33-8. doi: 10.3341/kjo.2007.21.1.33. Korean J Ophthalmol. 2007. PMID: 17460430 Free PMC article.

2

Leber's hereditary optic neuropathy with 3460 mitochondrial DNA mutation.

Hwang JM, Chang BL, Koh HJ, Kim JY, Park SS. Hwang JM, et al. Among authors: park ss. J Korean Med Sci. 2002 Apr;17(2):283-6. doi: 10.3346/jkms.2002.17.2.283. J Korean Med Sci. 2002. PMID: 11961321 Free PMC article.

3

Mitochondrial DNA C4171A/ND1 is a novel primary causative mutation of Leber's hereditary optic neuropathy with a good prognosis.

Kim JY, Hwang JM, Park SS. Kim JY, et al. Among authors: park ss. Ann Neurol. 2002 May;51(5):630-4. doi: 10.1002/ana.10177. Ann Neurol. 2002. PMID: 12112111

4

Beta-thalassemia in the Korean population.

Park SS, Lee YJ, Kim JY, Joo SI, Hattori Y, Ohba Y, Cho HI. Park SS, et al. Hemoglobin. 2002 May;26(2):135-45. doi: 10.1081/hem-120005451. Hemoglobin. 2002. PMID: 12144056

5

RFLP haplotypes of beta-globin gene complex of beta-thalassemic chromosomes in Koreans.

Lee YJ, Park SS, Kim JY, Cho HI. Lee YJ, et al. Among authors: park ss. J Korean Med Sci. 2002 Aug;17(4):475-8. doi: 10.3346/jkms.2002.17.4.475. J Korean Med Sci. 2002. PMID: 12172041 Free PMC article.

6

Spectrum of the mitochondrial DNA mutations of Leber's hereditary optic neuropathy in Koreans.

Kim JY, Hwang JM, Chang BL, Park SS. Kim JY, et al. Among authors: park ss. J Neurol. 2003 Mar;250(3):278-81. doi: 10.1007/s00415-003-0985-4. J Neurol. 2003. PMID: 12638016

7

Investigation of the association between OPA1 polymorphisms and normal-tension glaucoma in Korea.

Woo SJ, Kim DM, Kim JY, Park SS, Ko HS, Yoo T. Woo SJ, et al. Among authors: park ss. J Glaucoma. 2004 Dec;13(6):492-5. doi: 10.1097/01.ijg.0000137870.25779.40. J Glaucoma. 2004. PMID: 15534475

8

Molecular characterization of D- Korean persons: development of a diagnostic strategy.

Kim JY, Kim SY, Kim CA, Yon GS, Park SS. Kim JY, et al. Among authors: park ss. Transfusion. 2005 Mar;45(3):345-52. doi: 10.1111/j.1537-2995.2005.04311.x. Transfusion. 2005. PMID: 15752151

9

Investigations on the association between normal tension glaucoma and single nucleotide polymorphisms of the endothelin-1 and endothelin receptor genes.

Kim SH, Kim JY, Kim DM, Ko HS, Kim SY, Yoo T, Hwang SS, Park SS. Kim SH, et al. Among authors: park ss. Mol Vis. 2006 Aug 29;12:1016-21. Mol Vis. 2006. PMID: 16971893 Free article.

10

Molecular characterization of Leber congenital amaurosis in Koreans.

Seong MW, Kim SY, Yu YS, Hwang JM, Kim JY, Park SS. Seong MW, et al. Among authors: park ss. Mol Vis. 2008 Aug 4;14:1429-36. Mol Vis. 2008. PMID: 18682808 Free PMC article.

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