Park SS - Search Results

1

Genetic Mutation Profiles in Korean Patients with Inherited Retinal Diseases.

Kim MS, Joo K, Seong MW, Kim MJ, Park KH, Park SS, Woo SJ. Kim MS, et al. Among authors: park ss, park kh. J Korean Med Sci. 2019 Jun 2;34(21):e161. doi: 10.3346/jkms.2019.34.e161. J Korean Med Sci. 2019. PMID: 31144483 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

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.

4

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

5

Neonatal intrahepatic cholestasis caused by citrin deficiency in Korean infants.

Ko JS, Song JH, Park SS, Seo JK. Ko JS, et al. Among authors: park ss. J Korean Med Sci. 2007 Dec;22(6):952-6. doi: 10.3346/jkms.2007.22.6.952. J Korean Med Sci. 2007. PMID: 18162705 Free PMC article.

6

Molecular genetic characteristics of X-linked retinoschisis in Koreans.

Kim SY, Ko HS, Yu YS, Hwang JM, Lee JJ, Kim SY, Kim JY, Seong MW, Park KH, Park SS. Kim SY, et al. Among authors: park ss, park kh. Mol Vis. 2009;15:833-43. Epub 2009 Apr 23. Mol Vis. 2009. PMID: 19390641 Free PMC article.

7

Childhood brugada syndrome in two korean families.

Lee YS, Baek JS, Kim SY, Seo SW, Kwon BS, Kim GB, Bae EJ, Park SS, Noh CI. Lee YS, et al. Among authors: park ss. Korean Circ J. 2010 Mar;40(3):143-7. doi: 10.4070/kcj.2010.40.3.143. Epub 2010 Mar 24. Korean Circ J. 2010. PMID: 20339501 Free PMC article.

8

Molecular characterization of the NF2 gene in Korean patients with neurofibromatosis type 2: a report of four novel mutations.

Seong MW, Yeo IK, Cho SI, Park CK, Kim SK, Paek SH, Kim DG, Jung HW, Park H, Kim SY, Kim JY, Park SS. Seong MW, et al. Among authors: park ss, park ck, park h. Korean J Lab Med. 2010 Apr;30(2):190-4. doi: 10.3343/kjlm.2010.30.2.190. Korean J Lab Med. 2010. PMID: 20445339

9

Glutaric aciduria type 1 in Korea: report of two novel mutations.

Park JD, Lim B, Kim KJ, Hwang YS, Kim SK, Kang SH, Cho SI, Park SS, Lee JS, Chae JH. Park JD, et al. Among authors: park ss. J Korean Med Sci. 2010 Jun;25(6):957-60. doi: 10.3346/jkms.2010.25.6.957. Epub 2010 May 24. J Korean Med Sci. 2010. PMID: 20514322 Free PMC article.

10

Autosomal recessive multiple epiphyseal dysplasia in a Korean girl caused by novel compound heterozygous mutations in the DTDST (SLC26A2) gene.

Cho TJ, Kim OH, Lee HR, Shin SJ, Yoo WJ, Park WY, Park SS, Cho SI, Choi IH. Cho TJ, et al. Among authors: park ss, park wy. J Korean Med Sci. 2010 Jul;25(7):1105-8. doi: 10.3346/jkms.2010.25.7.1105. Epub 2010 Jun 16. J Korean Med Sci. 2010. PMID: 20592910 Free PMC article.

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