Yoo EH - Search Results

1

A novel mutation W252X in the WAS gene in a Korean patient with Wiskott-Aldrich syndrome.

Kim HJ, Yoo EH, Ki CS, Yoo GH, Koo HH, Kim JW, Kim SH. Kim HJ, et al. Among authors: yoo gh, yoo eh. Int J Hematol. 2006 Jun;83(5):426-8. doi: 10.1532/IJH97.A30513. Int J Hematol. 2006. PMID: 16787874

2

JAK2 V617F and MPL W515L/K mutations in Korean patients with essential thrombocythemia.

Kim HJ, Jang JH, Yoo EH, Kim HJ, Ki CS, Kim JW, Kim SH. Kim HJ, et al. Among authors: yoo eh. Korean J Lab Med. 2010 Oct;30(5):474-6. doi: 10.3343/kjlm.2010.30.5.474. Korean J Lab Med. 2010. PMID: 20890078

3

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. Among authors: yoo eh. 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.

4

Isobutyryl-CoA dehydrogenase deficiency with a novel ACAD8 gene mutation detected by tandem mass spectrometry newborn screening.

Yoo EH, Cho HJ, Ki CS, Lee SY. Yoo EH, et al. Clin Chem Lab Med. 2007;45(11):1495-7. doi: 10.1515/CCLM.2007.317. Clin Chem Lab Med. 2007. PMID: 17924841

5

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: yoo eh. 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.

6

A novel initiation codon mutation in the ribosomal protein S17 gene (RPS17) in a patient with Diamond-Blackfan anemia.

Song MJ, Yoo EH, Lee KO, Kim GN, Kim HJ, Kim SY, Kim SH. Song MJ, et al. Among authors: yoo eh. Pediatr Blood Cancer. 2010 Apr;54(4):629-31. doi: 10.1002/pbc.22316. Pediatr Blood Cancer. 2010. PMID: 19953637

7

Acute myeloid leukemia with del(X)(p21) and cryptic RUNX1/RUNX1T1 from ins(8;21)(q22;q22q22) revealed by atypical FISH signals.

Jang JH, Yoo EH, Kim HJ, Kim DH, Jung CW, Kim SH. Jang JH, et al. Among authors: yoo eh. Ann Clin Lab Sci. 2010 Winter;40(1):80-4. Ann Clin Lab Sci. 2010. PMID: 20124335

8

Clinical, pathological, and genetic analysis of a Korean family with thoracic aortic aneurysms and dissections carrying a novel Asp26Tyr mutation.

Yoo EH, Choi SH, Jang SY, Suh YL, Lee I, Song JK, Choe YH, Kim JW, Ki CS, Kim DK. Yoo EH, et al. Ann Clin Lab Sci. 2010 Summer;40(3):278-84. Ann Clin Lab Sci. 2010. PMID: 20689142

9

Frequent CD7 antigen loss in aggressive natural killer-cell leukemia: a useful diagnostic marker.

Yoo EH, Kim HJ, Lee ST, Kim WS, Kim SH. Yoo EH, et al. Korean J Lab Med. 2009 Dec;29(6):491-6. doi: 10.3343/kjlm.2009.29.6.491. Korean J Lab Med. 2009. PMID: 20046078

10

Genetic Characteristics of Polycythemia Vera and Essential Thrombocythemia in Korean Patients.

Yoo EH, Park KJ, Won HH, Park JH, Park JH, Lee ST, Kim HJ, Bang SM, Chi HS, Jung CW, Kim SH, Yun H, Sun CH, Park I, Lee S, Lee C, Merriman B, Luo R, Tan EH, Park KJ, Yoo NK, Kang JJ, Kim JW. Yoo EH, et al. Among authors: yoo nk. J Clin Lab Anal. 2016 Nov;30(6):1061-1070. doi: 10.1002/jcla.21981. Epub 2016 May 2. J Clin Lab Anal. 2016. PMID: 27132877 Free PMC article.

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