Kim SY - Search Results

1

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: kim sy, kim gb. 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.

2

Molecular and clinical characteristics of myotonic dystrophy type 1 in koreans.

Kim SY, Kim JY, Kim GP, Sung JJ, Lim KS, Lee KW, Chae JH, Hong YH, Seong MW, Park SS. Kim SY, et al. Among authors: kim jy, kim gp. Korean J Lab Med. 2008 Dec;28(6):483-92. doi: 10.3343/kjlm.2008.28.6.483. Korean J Lab Med. 2008. PMID: 19127114

3

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: kim jy. Mol Vis. 2009;15:833-43. Epub 2009 Apr 23. Mol Vis. 2009. PMID: 19390641 Free PMC article.

4

Infantile vitreous hemorrhage as the initial presentation of X-linked juvenile retinoschisis.

Lee JJ, Kim JH, Kim SY, Park SS, Yu YS. Lee JJ, et al. Among authors: kim sy, kim jh. Korean J Ophthalmol. 2009 Jun;23(2):118-20. doi: 10.3341/kjo.2009.23.2.118. Epub 2009 Jun 9. Korean J Ophthalmol. 2009. PMID: 19568363 Free PMC article.

5

False homozygous deletions of SMN1 exon 7 using Dra I PCR-RFLP caused by a novel mutation in spinal muscular atrophy.

Kang SH, Cho SI, Chae JH, Chung KN, Ra EK, Kim SY, Seong MW, Kim JY, Park SS. Kang SH, et al. Among authors: kim jy, kim sy. Genet Test Mol Biomarkers. 2009 Aug;13(4):511-3. doi: 10.1089/gtmb.2008.0158. Genet Test Mol Biomarkers. 2009. PMID: 19663601

6

Low contribution of BRCA1/2 genomic rearrangement to high-risk breast cancer in the Korean population.

Seong MW, Cho SI, Noh DY, Han W, Kim SW, Park CM, Park HW, Kim SY, Kim JY, Park SS. Seong MW, et al. Among authors: kim jy, kim sw, kim sy. Fam Cancer. 2009;8(4):505-8. doi: 10.1007/s10689-009-9279-z. Epub 2009 Aug 8. Fam Cancer. 2009. PMID: 19669600

7

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: kim jy, kim dg, kim sy, kim sk. 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

8

Jervell and Lange-Nielsen syndrome: novel compound heterozygous mutations in the KCNQ1 in a Korean family.

Baek JS, Bae EJ, Lee SY, Park SS, Kim SY, Jung KN, Noh CI. Baek JS, et al. Among authors: kim sy. J Korean Med Sci. 2010 Oct;25(10):1522-5. doi: 10.3346/jkms.2010.25.10.1522. Epub 2010 Sep 20. J Korean Med Sci. 2010. PMID: 20890437 Free PMC article.

9

Molecular identification of the novel Gγ-β hybrid hemoglobin: Hb Gγ-β Ulsan (Gγ through 13; β from 19).

Kim SY, Lee SH, Cho SI, Song SH, Hattori Y, Park SK, Song J, Choi Y, Yang M, Park H, Kim SR, Seong MW, Kim JY, Cho HI, Park SS. Kim SY, et al. Among authors: kim sr, kim jy. Blood Cells Mol Dis. 2010 Dec 15;45(4):276-9. doi: 10.1016/j.bcmd.2010.10.001. Epub 2010 Oct 29. Blood Cells Mol Dis. 2010. PMID: 21035360

10

A case of brain abscess caused by Propionibacterium acnes 13 months after neurosurgery and confirmed by 16S rRNA gene sequencing.

Chung S, Kim JS, Seo SW, Ra EK, Joo SI, Kim SY, Park SS, Kim EC. Chung S, et al. Among authors: kim sy, kim js, kim ec. Korean J Lab Med. 2011 Apr;31(2):122-6. doi: 10.3343/kjlm.2011.31.2.122. Korean J Lab Med. 2011. PMID: 21474989 Free PMC article.

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