Kim JW - Search Results

1

Fukutin mutations in congenital muscular dystrophies with defective glycosylation of dystroglycan in Korea.

Lim BC, Ki CS, Kim JW, Cho A, Kim MJ, Hwang H, Kim KJ, Hwang YS, Park WY, Lim YJ, Kim IO, Lee JS, Chae JH. Lim BC, et al. Among authors: kim kj, kim io, kim jw, kim mj. Neuromuscul Disord. 2010 Aug;20(8):524-30. doi: 10.1016/j.nmd.2010.06.005. Neuromuscul Disord. 2010. PMID: 20620061

2

Genetic association of an apolipoprotein C-I (APOC1) gene polymorphism with late-onset Alzheimer's disease.

Ki CS, Na DL, Kim DK, Kim HJ, Kim JW. Ki CS, et al. Among authors: kim hj, kim dk, kim jw. Neurosci Lett. 2002 Feb 15;319(2):75-8. doi: 10.1016/s0304-3940(01)02559-9. Neurosci Lett. 2002. PMID: 11825674

3

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.

4

A novel missense mutation (I344K) in the SPG4gene in a Korean family with autosomal-dominant hereditary spastic paraplegia.

Ki CS, Lee WY, Han DH, Sung DH, Lee KB, Lee KA, Cho SS, Cho S, Hwang H, Sohn KM, Choi YJ, Kim JW. Ki CS, et al. Among authors: kim jw. J Hum Genet. 2002;47(9):473-7. doi: 10.1007/s100380200068. J Hum Genet. 2002. PMID: 12202986

5

A novel mutation (C67Y)in the NOTCH3 gene in a Korean CADASIL patient.

Moon SY, Kim HY, Seok JI, Kwon JC, Ki CS, Kim JW, Suh YL, Na DL. Moon SY, et al. Among authors: kim hy, kim jw. J Korean Med Sci. 2003 Feb;18(1):141-4. doi: 10.3346/jkms.2003.18.1.141. J Korean Med Sci. 2003. PMID: 12589106 Free PMC article.

6

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.

7

A novel point mutation in PMP22 gene associated with a familial case of Charcot-Marie-Tooth disease type 1A with sensorineural deafness.

Joo IS, Ki CS, Joo SY, Huh K, Kim JW. Joo IS, et al. Among authors: kim jw. Neuromuscul Disord. 2004 May;14(5):325-8. doi: 10.1016/j.nmd.2004.02.009. Neuromuscul Disord. 2004. PMID: 15099592

8

Novel interleukin 1beta polymorphism increased the risk of gastric cancer in a Korean population.

Lee KA, Ki CS, Kim HJ, Sohn KM, Kim JW, Kang WK, Rhee JC, Song SY, Sohn TS. Lee KA, et al. Among authors: kim hj, kim jw. J Gastroenterol. 2004;39(5):429-33. doi: 10.1007/s00535-003-1315-4. J Gastroenterol. 2004. PMID: 15175940

9

Evaluation of imprecision for analysis of short tandem repeats by use of mixed blood cells in variable concentrations.

Kong SY, Ki CS, Kim HJ, Lee KO, Bae JC, Kim SH, Kim JW. Kong SY, et al. Among authors: kim hj, kim sh, kim jw. Clin Chem. 2004 Nov;50(11):2193-5. doi: 10.1373/clinchem.2004.036103. Clin Chem. 2004. PMID: 15502099 No abstract available.

10

RET proto-oncogene mutations are restricted to codon 634 and 618 in Korean families with multiple endocrine neoplasia 2A.

Chung YJ, Kim HH, Kim HJ, Min YK, Lee MS, Lee MK, Kim KW, Ki CS, Kim JW, Chung JH. Chung YJ, et al. Among authors: kim hh, kim hj, kim kw, kim jw. Thyroid. 2004 Oct;14(10):813-8. doi: 10.1089/thy.2004.14.813. Thyroid. 2004. PMID: 15588376

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