Park SS - Search Results

1

Viral RNA Load in Mildly Symptomatic and Asymptomatic Children with COVID-19, Seoul, South Korea.

Han MS, Seong MW, Kim N, Shin S, Cho SI, Park H, Kim TS, Park SS, Choi EH. Han MS, et al. Among authors: park ss, park h. Emerg Infect Dis. 2020 Oct;26(10):2497-2499. doi: 10.3201/eid2610.202449. Epub 2020 Jun 4. Emerg Infect Dis. 2020. PMID: 32497001 Free PMC article.

2

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.

3

LCA5, a rare genetic cause 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. Ophthalmic Genet. 2009 Mar;30(1):54-5. doi: 10.1080/13816810802592567. Ophthalmic Genet. 2009. PMID: 19172513

4

Ophthalmoplegia diagnosis.

Hwang JM, Choung HK, Ko HS, Seong MW, Kim JY, Park SS. Hwang JM, et al. Among authors: park ss. Ophthalmology. 2009 Apr;116(4):813-4, 814.e1-2. doi: 10.1016/j.ophtha.2008.12.006. Ophthalmology. 2009. PMID: 19344829 No abstract available.

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: park ss. 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: park ss, park hw, park cm. Fam Cancer. 2009;8(4):505-8. doi: 10.1007/s10689-009-9279-z. Epub 2009 Aug 8. Fam Cancer. 2009. PMID: 19669600

7

Screening for MAPT and PGRN mutations in Korean patients with PSP/CBS/FTD.

Kim HJ, Jeon BS, Yun JY, Seong MW, Park SS, Lee JY. Kim HJ, et al. Among authors: park ss. Parkinsonism Relat Disord. 2010 May;16(4):305-6. doi: 10.1016/j.parkreldis.2010.01.004. Epub 2010 Feb 19. Parkinsonism Relat Disord. 2010. PMID: 20171924 No abstract available.

8

Predicted pathogenic missense mutation of PGRN found in a normal control.

Kim HJ, Seong MW, Yun JY, Park SS, Lee JY, Jeon BS. Kim HJ, et al. Among authors: park ss. Ann Neurol. 2010 Mar;67(3):415-6. doi: 10.1002/ana.21892. Ann Neurol. 2010. PMID: 20373362 No abstract available.

9

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

10

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: park ss, park sk, park h. 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

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