Lee ST - Search Results

1

BRAF V600E and MAP2K1 mutations in hairy cell leukemia and splenic marginal zone lymphoma cases.

Shin SY, Lee ST, Kim HJ, Ki CS, Jung CW, Kim JW, Kim SH. Shin SY, et al. Among authors: lee st. Ann Lab Med. 2015 Mar;35(2):257-9. doi: 10.3343/alm.2015.35.2.257. Epub 2015 Feb 12. Ann Lab Med. 2015. PMID: 25729732 Free PMC article. No abstract available.

2

Incidence of variant hemoglobin (Hb) and increased fetal Hb concentrations and their effect on Hb A1c measurement in a Korean population.

Lee ST, Kim MS, Choi DY, Kim SK, Ki CS. Lee ST, et al. Clin Chem. 2006 Jul;52(7):1445-6. doi: 10.1373/clinchem.2006.069617. Clin Chem. 2006. PMID: 16798979 No abstract available.

3

Contributions of CYP2C9/CYP2C19 genotypes and drug interaction to the phenytoin treatment in the Korean epileptic patients in the clinical setting.

Lee SY, Lee ST, Kim JW. Lee SY, et al. Among authors: lee st. J Biochem Mol Biol. 2007 May 31;40(3):448-52. doi: 10.5483/bmbrep.2007.40.3.448. J Biochem Mol Biol. 2007. PMID: 17562299

4

Effects of 7 hemoglobin variants on the measurement of glycohemoglobin by 14 analytical methods.

Lee ST, Weykamp CW, Lee YW, Kim JW, Ki CS. Lee ST, et al. Among authors: lee yw. Clin Chem. 2007 Dec;53(12):2202-5. doi: 10.1373/clinchem.2007.093963. Epub 2007 Oct 5. Clin Chem. 2007. PMID: 17921258

5

Identification of an Arg35X mutation in the PDCD10 gene in a patient with cerebral and multiple spinal cavernous malformations.

Lee ST, Choi KW, Yeo HT, Kim JW, Ki CS, Cho YD. Lee ST, et al. J Neurol Sci. 2008 Apr 15;267(1-2):177-81. doi: 10.1016/j.jns.2007.10.018. Epub 2007 Nov 26. J Neurol Sci. 2008. PMID: 18035376

6

High oxygen-affinity hemoglobin variant associated with high-level venous oxygen saturation.

Lee YW, Ki CS, Kim HJ, Lee ST, Kim CK, Shin HB, Hong DS, Lee YK. Lee YW, et al. Among authors: lee st, lee yk. Clin Chem Lab Med. 2008;46(3):417-8. doi: 10.1515/CCLM.2008.066. Clin Chem Lab Med. 2008. PMID: 18254704 No abstract available.

7

A novel COL3A1 gene mutation in patient with aortic dissected aneurysm and cervical artery dissections.

Lee ST, Kim JA, Jang SY, Kim DK, Kim JW, Ki CS. Lee ST, et al. Heart Vessels. 2008 Mar;23(2):144-8. doi: 10.1007/s00380-007-1027-4. Epub 2008 Apr 4. Heart Vessels. 2008. PMID: 18389341

8

A novel mutation Ala57Val of the ELA2 gene in a Korean boy with severe congenital neutropenia.

Lee ST, Yoon HS, Kim HJ, Lee JH, Park JH, Kim SH, Seo JJ, Im HJ. Lee ST, et al. Among authors: lee jh. Ann Hematol. 2009 Jun;88(6):593-5. doi: 10.1007/s00277-008-0629-y. Epub 2008 Oct 23. Ann Hematol. 2009. PMID: 18946670 No abstract available.

9

Clinical and genetic analysis of Korean patients with facioscapulohumeral muscular dystrophy.

Ki CS, Lee ST, Kim KS, Kim JW, Hong YH, Sung JJ, Park KS, Lee KW. Ki CS, et al. Among authors: lee kw, lee st. J Korean Med Sci. 2008 Dec;23(6):959-63. doi: 10.3346/jkms.2008.23.6.959. Epub 2008 Dec 23. J Korean Med Sci. 2008. PMID: 19119436 Free PMC article.

10

Clinical features and mutations in the ENG, ACVRL1, and SMAD4 genes in Korean patients with hereditary hemorrhagic telangiectasia.

Lee ST, Kim JA, Jang SY, Kim DK, Do YS, Suh GY, Kim JW, Ki CS. Lee ST, et al. J Korean Med Sci. 2009 Feb;24(1):69-76. doi: 10.3346/jkms.2009.24.1.69. Epub 2009 Feb 28. J Korean Med Sci. 2009. PMID: 19270816 Free PMC article.

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