Kim JW - Search Results

1

Clinical, biochemical, and genetic analysis of korean patients with pseudohypoparathyroidism type Ia.

Park CH, Park HD, Lee SY, Kim JW, Sohn YB, Park SW, Jin DK. Park CH, et al. Among authors: kim jw. Ann Clin Lab Sci. 2010 Summer;40(3):261-6. Ann Clin Lab Sci. 2010. PMID: 20689139

2

Complete sequencing of a genetic polymorphism in NAT2 in the Korean population.

Lee SY, Lee KA, Ki CS, Kwon OJ, Kim HJ, Chung MP, Suh GY, Kim JW. Lee SY, et al. Among authors: kim hj, kim jw. Clin Chem. 2002 May;48(5):775-7. Clin Chem. 2002. PMID: 11978608 No abstract available.

3

Haplotype structure of the UDP-glucuronosyltransferase 1A1 (UGT1A1) gene and its relationship to serum total bilirubin concentration in a male Korean population.

Ki CS, Lee KA, Lee SY, Kim HJ, Cho SS, Park JH, Cho S, Sohn KM, Kim JW. Ki CS, et al. Among authors: kim hj, kim jw. Clin Chem. 2003 Dec;49(12):2078-81. doi: 10.1373/clinchem.2003.024174. Clin Chem. 2003. PMID: 14633881 No abstract available.

4

A novel mutation (A148V) in the glucose 6-phosphate translocase (SLC37A4) gene in a Korean patient with glycogen storage disease type 1b.

Han SH, Ki CS, Lee JE, Hong YJ, Son BK, Lee KH, Choe YH, Lee SY, Kim JW. Han SH, et al. Among authors: kim jw. J Korean Med Sci. 2005 Jun;20(3):499-501. doi: 10.3346/jkms.2005.20.3.499. J Korean Med Sci. 2005. PMID: 15953877 Free PMC article.

5

Mutation analysis of SPG4 and SPG3A genes and its implication in molecular diagnosis of Korean patients with hereditary spastic paraplegia.

Park SY, Ki CS, Kim HJ, Kim JW, Sung DH, Kim BJ, Lee WY. Park SY, et al. Among authors: kim hj, kim bj, kim jw. Arch Neurol. 2005 Jul;62(7):1118-21. doi: 10.1001/archneur.62.7.1118. Arch Neurol. 2005. PMID: 16009769

6

GSTM1, GSTT1 and GSTP1 polymorphisms in the Korean population.

Cho HJ, Lee SY, Ki CS, Kim JW. Cho HJ, et al. Among authors: kim jw. J Korean Med Sci. 2005 Dec;20(6):1089-92. doi: 10.3346/jkms.2005.20.6.1089. J Korean Med Sci. 2005. PMID: 16361831 Free PMC article.

7

A case of intolerance to warfarin dosing in an intermediate metabolizer of CYP2C9.

Lee SY, Kim JS, Kim JW. Lee SY, et al. Among authors: kim js, kim jw. Yonsei Med J. 2005 Dec 31;46(6):843-6. doi: 10.3349/ymj.2005.46.6.843. Yonsei Med J. 2005. PMID: 16385662 Free PMC article.

8

Sequence-based CYP2D6 genotyping in the Korean population.

Lee SY, Sohn KM, Ryu JY, Yoon YR, Shin JG, Kim JW. Lee SY, et al. Among authors: kim jw. Ther Drug Monit. 2006 Jun;28(3):382-7. doi: 10.1097/01.ftd.0000211823.80854.db. Ther Drug Monit. 2006. PMID: 16778723

9

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

10

Clinical and genetic analysis of Korean patients with Miyoshi myopathy: identification of three novel mutations in the DYSF gene.

Cho HJ, Sung DH, Kim EJ, Yoon CH, Ki CS, Kim JW. Cho HJ, et al. Among authors: kim ej, kim jw. J Korean Med Sci. 2006 Aug;21(4):724-7. doi: 10.3346/jkms.2006.21.4.724. J Korean Med Sci. 2006. PMID: 16891820 Free PMC article.

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