Kim JW - Search Results

1

A polymorphism in the growth hormone receptor is associated with height in children with Prader-Willi syndrome.

Park SW, Lee ST, Sohn YB, Kim SH, Cho SY, Ko AR, Ji ST, Kwon JY, Yeau S, Paik KH, Kim JW, Jin DK. Park SW, et al. Among authors: kim sh, kim jw. Am J Med Genet A. 2011 Dec;155A(12):2970-3. doi: 10.1002/ajmg.a.34309. Epub 2011 Nov 3. Am J Med Genet A. 2011. PMID: 22052808

2

Characterization of late-onset citrullinemia 1 in a Korean patient: confirmation by argininosuccinate synthetase gene mutation analysis.

Kim IS, Ki CS, Kim JW, Lee M, Jin DK, Lee SY. Kim IS, et al. Among authors: kim jw. J Biochem Mol Biol. 2006 Jul 31;39(4):400-5. doi: 10.5483/bmbrep.2006.39.4.400. J Biochem Mol Biol. 2006. PMID: 16889683

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: kim jw. 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: kim jw. 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. Among authors: kim jw. 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

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. Among authors: kim ja, kim dk, kim jw. Heart Vessels. 2008 Mar;23(2):144-8. doi: 10.1007/s00380-007-1027-4. Epub 2008 Apr 4. Heart Vessels. 2008. PMID: 18389341

7

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: kim ks, kim jw. 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.

8

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. Among authors: kim ja, kim dk, kim jw. 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.

9

Clinical and genetic analysis of Korean patients with congenital insensitivity to pain with anhidrosis.

Lee ST, Lee J, Lee M, Kim JW, Ki CS. Lee ST, et al. Among authors: kim jw. Muscle Nerve. 2009 Nov;40(5):855-9. doi: 10.1002/mus.21340. Muscle Nerve. 2009. PMID: 19618435

10

Multiplex ligation-dependent probe amplification screening of isolated increased HbF levels revealed three cases of novel rearrangements/deletions in the beta-globin gene cluster.

Lee ST, Yoo EH, Kim JY, Kim JW, Ki CS. Lee ST, et al. Among authors: kim jy, kim jw. Br J Haematol. 2010 Jan;148(1):154-60. doi: 10.1111/j.1365-2141.2009.07927.x. Epub 2009 Oct 5. Br J Haematol. 2010. PMID: 19807730 Free article.

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

8,985 results

Search Page

Filters