Ki CS - Search Results

1

PSEN1 variants in Korean patients with clinically suspicious early-onset familial Alzheimer's disease.

Kim YE, Cho H, Kim HJ, Na DL, Seo SW, Ki CS. Kim YE, et al. Among authors: ki cs. Sci Rep. 2020 Feb 26;10(1):3480. doi: 10.1038/s41598-020-59829-z. Sci Rep. 2020. PMID: 32103039 Free PMC article.

2

Genetic association of an apolipoprotein C-I (APOC1) gene polymorphism with late-onset Alzheimer's disease.

Ki CS, Na DL, Kim DK, Kim HJ, Kim JW. Ki CS, et al. Neurosci Lett. 2002 Feb 15;319(2):75-8. doi: 10.1016/s0304-3940(01)02559-9. Neurosci Lett. 2002. PMID: 11825674

3

A novel mutation (C67Y)in the NOTCH3 gene in a Korean CADASIL patient.

Moon SY, Kim HY, Seok JI, Kwon JC, Ki CS, Kim JW, Suh YL, Na DL. Moon SY, et al. Among authors: ki cs. J Korean Med Sci. 2003 Feb;18(1):141-4. doi: 10.3346/jkms.2003.18.1.141. J Korean Med Sci. 2003. PMID: 12589106 Free PMC article.

4

Clinical and genetic analysis of HLXB9 gene in Korean patients with Currarino syndrome.

Kim IS, Oh SY, Choi SJ, Kim JH, Park KH, Park HK, Kim JW, Ki CS. Kim IS, et al. Among authors: ki cs. J Hum Genet. 2007;52(8):698-701. doi: 10.1007/s10038-007-0173-y. Epub 2007 Jul 6. J Hum Genet. 2007. PMID: 17612791

5

Identification of PSEN1 and APP gene mutations in Korean patients with early-onset Alzheimer's disease.

Park HK, Na DL, Lee JH, Kim JW, Ki CS. Park HK, et al. Among authors: ki cs. J Korean Med Sci. 2008 Apr;23(2):213-7. doi: 10.3346/jkms.2008.23.2.213. J Korean Med Sci. 2008. PMID: 18437002 Free PMC article.

6

Presenilin 1 gene mutation (M139I) in a patient with an early-onset Alzheimer's disease: clinical characteristics and genetic identification.

Kim HJ, Kim HY, Ki CS, Kim SH. Kim HJ, et al. Among authors: ki cs. Neurol Sci. 2010 Dec;31(6):781-3. doi: 10.1007/s10072-010-0233-5. Epub 2010 Mar 6. Neurol Sci. 2010. PMID: 20213228

7

Heterogeneous spectrum of CFTR gene mutations in Korean patients with cystic fibrosis.

Jung H, Ki CS, Koh WJ, Ahn KM, Lee SI, Kim JH, Ko JS, Seo JK, Cha SI, Lee ES, Kim JW. Jung H, et al. Among authors: ki cs. Korean J Lab Med. 2011 Jul;31(3):219-24. doi: 10.3343/kjlm.2011.31.3.219. Epub 2011 Jun 28. Korean J Lab Med. 2011. PMID: 21779199 Free PMC article.

8

Three Korean patients with maple syrup urine disease: four novel mutations in the BCKDHA gene.

Park HD, Lee DH, Hong YH, Kang DH, Lee YK, Song J, Lee SY, Kim JW, Ki CS, Lee YW. Park HD, et al. Among authors: ki cs. Ann Clin Lab Sci. 2011 Spring;41(2):167-73. Ann Clin Lab Sci. 2011. PMID: 21844576

9

Toll-like receptor 4 gene polymorphisms do not associate with normal tension glaucoma in a Korean population.

Suh W, Kim S, Ki CS, Kee C. Suh W, et al. Among authors: ki cs. Mol Vis. 2011;17:2343-8. Epub 2011 Aug 31. Mol Vis. 2011. PMID: 21921986 Free PMC article.

10

Screening of the SOD1, FUS, TARDBP, ANG, and OPTN mutations in Korean patients with familial and sporadic ALS.

Kwon MJ, Baek W, Ki CS, Kim HY, Koh SH, Kim JW, Kim SH. Kwon MJ, et al. Among authors: ki cs. Neurobiol Aging. 2012 May;33(5):1017.e17-23. doi: 10.1016/j.neurobiolaging.2011.12.003. Epub 2012 Jan 15. Neurobiol Aging. 2012. PMID: 22244934

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