Jang MA - Search Results

1

Chronic lymphocytic leukemia in Korean patients: frequent atypical immunophenotype and relatively aggressive clinical behavior.

Jang MA, Yoo EH, Kim K, Kim WS, Jung CW, Kim SH, Kim HJ. Jang MA, et al. Int J Hematol. 2013 Mar;97(3):403-8. doi: 10.1007/s12185-013-1286-z. Epub 2013 Feb 12. Int J Hematol. 2013. PMID: 23400412 Clinical Trial.

2

A novel splice-site mutation c.42-2A>T (IVS1-2A>T) of SERPINC1 in a Korean family with inherited antithrombin deficiency.

Jang MJ, Lee JG, Chong SY, Huh JY, Jang MA, Kim HJ, Oh D. Jang MJ, et al. Among authors: jang ma. Blood Coagul Fibrinolysis. 2011 Dec;22(8):742-5. doi: 10.1097/MBC.0b013e32834a7e17. Blood Coagul Fibrinolysis. 2011. PMID: 21885952

3

Novel mutations in CEBPA in Korean Patients with acute myeloid leukemia with a normal karyotype.

Kim S, Kim DH, Jang JH, Jung CW, Jang MA, Ki CS, Kim JW, Kim SH, Kim HJ. Kim S, et al. Among authors: jang jh, jang ma. Ann Lab Med. 2012 Mar;32(2):153-7. doi: 10.3343/alm.2012.32.2.153. Epub 2012 Feb 23. Ann Lab Med. 2012. PMID: 22389883 Free PMC article.

4

Extra X chromosome in mosaic Klinefelter syndrome is associated with a hematologic malignancy.

Jang MA, Jung CW, Jung CW. Jang MA, et al. Ann Lab Med. 2013 Jul;33(4):297-9. doi: 10.3343/alm.2013.33.4.297. Epub 2013 Jun 24. Ann Lab Med. 2013. PMID: 23826569 Free PMC article. No abstract available.

5

A unique case of dendritic cell neoplasm from monocyte-derived myeloid origin with distinct immunophenotype and cytomorphology.

Jang MA, Lee ST, Jung CW, Kim SH. Jang MA, et al. Ann Hematol. 2014 May;93(5):877-8. doi: 10.1007/s00277-013-1903-1. Epub 2013 Sep 17. Ann Hematol. 2014. PMID: 24043117 No abstract available.

6

Sequence variation data of F8 and F9 genes in functionally validated control individuals: implications on the molecular diagnosis of hemophilia.

Seo JY, Jang MA, Kim HJ, Lee KO, Kim SH, Kim HJ. Seo JY, et al. Among authors: jang ma. Blood Res. 2013 Sep;48(3):206-10. doi: 10.5045/br.2013.48.3.206. Epub 2013 Sep 25. Blood Res. 2013. PMID: 24086941 Free PMC article.

7

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. Blood Coagul Fibrinolysis. 2015 Jan;26(1):46-9. doi: 10.1097/MBC.0000000000000171. Blood Coagul Fibrinolysis. 2015. PMID: 25004025

8

A novel nonsense mutation Tyr301* of PROS1 causing protein S deficiency.

Jang MA, Kim SH, Kim DK, Kim HJ. Jang MA, et al. Blood Coagul Fibrinolysis. 2015 Mar;26(2):223-4. doi: 10.1097/MBC.0000000000000217. Blood Coagul Fibrinolysis. 2015. PMID: 25255242

9

The first Korean case of childhood acute myeloid leukemia with inv(11)(p15q22)/NUP98-DDX10 rearrangement: a rare but recurrent genetic abnormality.

Choi R, Jang MA, Yoo KH, Lee ST, Kim HJ, Kim SH. Choi R, et al. Among authors: jang ma. Ann Lab Med. 2014 Nov;34(6):478-80. doi: 10.3343/alm.2014.34.6.478. Epub 2014 Oct 28. Ann Lab Med. 2014. PMID: 25368827 Free PMC article. No abstract available.

10

Simultaneous occurrence of angioimmunoblastic T-cell lymphoma and plasma cell leukemia.

Jang MA, Lee ST, Kim HJ, Kim S, Kim SH. Jang MA, et al. Ann Lab Med. 2015 Jan;35(1):149-51. doi: 10.3343/alm.2015.35.1.149. Epub 2014 Dec 8. Ann Lab Med. 2015. PMID: 25553298 Free PMC article. No abstract available.

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