Lee ST - Search Results

1

Clinical and genetic analysis of a Korean family with hereditary spastic paraplegia type 3.

Kwon MJ, Lee ST, Kim JW, Sung DH, Ki CS. Kwon MJ, et al. Among authors: lee st. Ann Clin Lab Sci. 2010 Fall;40(4):375-9. Ann Clin Lab Sci. 2010. PMID: 20947813

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

Genetic analysis of three Korean patients with clinical features of Ehlers-Danlos syndrome type IV.

Yang JH, Lee ST, Kim JA, Kim SH, Jang SY, Ki CS, Kim DK. Yang JH, et al. Among authors: lee st. J Korean Med Sci. 2007 Aug;22(4):698-705. doi: 10.3346/jkms.2007.22.4.698. J Korean Med Sci. 2007. PMID: 17728513 Free PMC article.

5

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

6

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

7

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.

8

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

9

Mutation analysis of PAH gene and characterization of a recurrent deletion mutation in Korean patients with phenylketonuria.

Lee YW, Lee DH, Kim ND, Lee ST, Ahn JY, Choi TY, Lee YK, Kim SH, Kim JW, Ki CS. Lee YW, et al. Among authors: lee dh, lee st, lee yk. Exp Mol Med. 2008 Oct 31;40(5):533-40. doi: 10.3858/emm.2008.40.5.533. Exp Mol Med. 2008. PMID: 18985011 Free PMC article.

10

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.

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