Lee KO - Search Results

1

Novel and recurrent mutations in the F13A1 gene in unrelated Korean patients with congenital factor XIII deficiency.

Jang MA, Park YS, Lee KO, Kim HJ. Jang MA, et al. Among authors: lee ko. Blood Coagul Fibrinolysis. 2015 Jan;26(1):46-9. doi: 10.1097/MBC.0000000000000171. Blood Coagul Fibrinolysis. 2015. PMID: 25004025

2

Molecular genetic analysis of Korean patients with coagulation factor XII deficiency.

Kwon MJ, Kim HJ, Lee KO, Jung CW, Kim SH. Kwon MJ, et al. Among authors: lee ko. Blood Coagul Fibrinolysis. 2010 Jun;21(4):308-12. doi: 10.1097/MBC.0b013e32833449df. Blood Coagul Fibrinolysis. 2010. PMID: 20386432

3

Novel deleterious mutation in the F12 gene in a Korean family with severe coagulation factor XII deficiency.

Kim HJ, Kim HJ, Kwon EH, Lee KO, Park IA, Kim SH. Kim HJ, et al. Among authors: lee ko. Blood Coagul Fibrinolysis. 2010 Oct;21(7):683-6. doi: 10.1097/MBC.0b013e32833e429c. Blood Coagul Fibrinolysis. 2010. PMID: 20729721

4

Recurrent mutations and genotype-phenotype correlations in hereditary factor VII deficiency in Korea.

Kwon MJ, Yoo KY, Lee KO, Kim SH, Kim HJ. Kwon MJ, et al. Among authors: lee ko. Blood Coagul Fibrinolysis. 2011 Mar;22(2):102-5. doi: 10.1097/MBC.0b013e328343641a. Blood Coagul Fibrinolysis. 2011. PMID: 21206266

5

Molecular characterization of female hemophilia A by multiplex ligation-dependent probe amplification analysis and X-chromosome inactivation study.

Song MJ, Kim HJ, Yoo KY, Park IA, Lee KO, Ki CS, Kim SH. Song MJ, et al. Among authors: lee ko. Blood Coagul Fibrinolysis. 2011 Apr;22(3):211-4. doi: 10.1097/MBC.0b013e328343f873. Blood Coagul Fibrinolysis. 2011. PMID: 21297454

6

Novel and recurrent mutations of ITGA2B and ITGB3 genes in Korean patients with Glanzmann thrombasthenia.

Park KJ, Chung HS, Lee KO, Park IA, Kim SH, Kim HJ. Park KJ, et al. Among authors: lee ko. Pediatr Blood Cancer. 2012 Aug;59(2):335-8. doi: 10.1002/pbc.24041. Epub 2011 Dec 20. Pediatr Blood Cancer. 2012. PMID: 22190468

7

Combined congenital dysfibrinogenemia and factor VII deficiency from mutations in the FGB and F7 genes.

Woo HI, Park IA, Lee KO, Kim SH, Kim HJ. Woo HI, et al. Among authors: lee ko. Blood Coagul Fibrinolysis. 2012 Jul;23(5):355-8. doi: 10.1097/MBC.0b013e32834fa81e. Blood Coagul Fibrinolysis. 2012. PMID: 22576285

8

Maternal low-level somatic mosaicism of Cys155Tyr of F9 in severe hemophilia B.

Kim HJ, Lee KO, Yoo KY, Kim SH, Kim HJ. Kim HJ, et al. Among authors: lee ko. Blood Coagul Fibrinolysis. 2015 Dec;26(8):866-8. doi: 10.1097/MBC.0000000000000234. Blood Coagul Fibrinolysis. 2015. PMID: 25402191

9

A Novel de novo Mutation in the G6PD Gene in a Korean Boy with Glucose-6-phosphate Dehydrogenase Deficiency: Case Report.

Jang MA, Kim JY, Lee KO, Kim SH, Koo HH, Kim HJ. Jang MA, et al. Among authors: lee ko. Ann Clin Lab Sci. 2015 Summer;45(4):446-8. Ann Clin Lab Sci. 2015. PMID: 26275698

10

Genetic Confirmation of Congenital Factor V Deficiency in Korean Patients.

Park CH, Yoo K, Lee KO, Kim SH, Sung KW, Kim HJ. Park CH, et al. Among authors: lee ko. Ann Lab Med. 2016 Mar;36(2):182-4. doi: 10.3343/alm.2016.36.2.182. Ann Lab Med. 2016. PMID: 26709270 Free PMC article. No abstract available.

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