Lee YW - Search Results

1

Molecular screening of the TSH receptor (TSHR) and thyroid peroxidase (TPO) genes in Korean patients with nonsyndromic congenital hypothyroidism.

Lee ST, Lee DH, Kim JY, Kwon MJ, Kim JW, Hong YH, Lee YW, Ki CS. Lee ST, et al. Among authors: lee dh, lee yw. Clin Endocrinol (Oxf). 2011 Nov;75(5):715-21. doi: 10.1111/j.1365-2265.2011.04156.x. Clin Endocrinol (Oxf). 2011. PMID: 21707688

2

Different spectrum of mutations of isovaleryl-CoA dehydrogenase (IVD) gene in Korean patients with isovaleric acidemia.

Lee YW, Lee DH, Vockley J, Kim ND, Lee YK, Ki CS. Lee YW, et al. Among authors: lee dh, lee yk. Mol Genet Metab. 2007 Sep-Oct;92(1-2):71-7. doi: 10.1016/j.ymgme.2007.05.003. Epub 2007 Jun 18. Mol Genet Metab. 2007. PMID: 17576084 Free PMC article.

3

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

4

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.

5

Mutation of Glu78 of the AVP-NPII gene impairs neurophysin as a carrier protein for arginine vasopressin in a family with neurohypophyseal diabetes insipidus.

Lee YW, Lee KW, Ryu JW, Mok JO, Ki CS, Park HK, Kim YJ, Kim SJ, Byun DW, Suh KI, Yoo MH, Shin HB, Lee YK, Kim CH. Lee YW, et al. Among authors: lee kw, lee yk. Ann Clin Lab Sci. 2008 Winter;38(1):12-4. Ann Clin Lab Sci. 2008. PMID: 18316776

6

Aspirin non-responsiveness in Korean subjects on dual anti-platelet treatment determined by two different platelet function assays.

Lee YW, Cho YH, Kim YH, Na JS, Shin HB, Ki CS, Choi TY, Lee YK. Lee YW, et al. Among authors: lee yk. Ann Clin Lab Sci. 2008 Spring;38(2):126-31. Ann Clin Lab Sci. 2008. PMID: 18469357

7

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.

8

Clinical, biochemical, and genetic analysis of a Korean neonate with hereditary tyrosinemia type 1.

Park HD, Lee DH, Choi TY, Lee YK, Kim JW, Ki CS, Lee YW. Park HD, et al. Among authors: lee dh, lee yw, lee yk. Clin Chem Lab Med. 2009;47(8):930-3. doi: 10.1515/CCLM.2009.223. Clin Chem Lab Med. 2009. PMID: 19569981

9

A novel KRIT1 gene mutation in a patient with cerebral and multiple spinal cavernous malformations.

Lee YW, Lee ST, Cha JG, Park JH, Jeon BR, Lee YK, Kim JW, Ki CS. Lee YW, et al. Among authors: lee st, lee yk. Ann Clin Lab Sci. 2010 Summer;40(3):290-4. Ann Clin Lab Sci. 2010. PMID: 20689144

10

Identification of a novel splicing mutation in the ARSA gene in a patient with late-infantile form of metachromatic leukodystrophy.

Kang DH, Lee DH, Hong YH, Lee ST, Jeon BR, Lee YK, Ki CS, Lee YW. Kang DH, et al. Among authors: lee dh, lee yw, lee st, lee yk. Korean J Lab Med. 2010 Oct;30(5):516-20. doi: 10.3343/kjlm.2010.30.5.516. Korean J Lab Med. 2010. PMID: 20890085

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

1,564 results

Search Page

Filters