Kim HJ - 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. Among authors: kim hj, kim sh, kim ws, kim k. 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

MLL/SEPTIN6 chimeric transcript from inv ins(X;11)(q24;q23q13) in acute monocytic leukemia: report of a case and review of the literature.

Kim HJ, Ki CS, Park Q, Koo HH, Yoo KH, Kim EJ, Kim SH. Kim HJ, et al. Among authors: kim ej, kim sh. Genes Chromosomes Cancer. 2003 Sep;38(1):8-12. doi: 10.1002/gcc.10235. Genes Chromosomes Cancer. 2003. PMID: 12874781 Review.

3

ABL oncogene amplification with p16(INK4a) gene deletion in precursor T-cell acute lymphoblastic leukemia/lymphoma: report of the first case.

Kim HJ, Woo HY, Koo HH, Tak EY, Kim SH. Kim HJ, et al. Among authors: kim sh. Am J Hematol. 2004 Aug;76(4):360-3. doi: 10.1002/ajh.20117. Am J Hematol. 2004. PMID: 15282669 Free article.

4

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.

5

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: kim sh, kim jw. Int J Hematol. 2006 Jun;83(5):426-8. doi: 10.1532/IJH97.A30513. Int J Hematol. 2006. PMID: 16787874

6

PML/RARA rearrangement associated with a t(15;19;17) in a case of acute myeloid leukemia with abundant myelocytes with salmon-pink cytoplasm.

Kim IS, Kim HJ, Choung HS, Jung CW, Kim JW, Kim SH. Kim IS, et al. Among authors: kim hj, kim sh, kim jw. Cancer Genet Cytogenet. 2006 Aug;169(1):81-2. doi: 10.1016/j.cancergencyto.2006.02.012. Cancer Genet Cytogenet. 2006. PMID: 16875944 No abstract available.

7

A boy with acute lymphoblastic leukemia acquired clonal and nonclonal cytogenetic abnormalities including del(7q) and del(20q) without clinical evidence of disease after sex-mismatched cord blood transplantation.

Kim IS, Kim HJ, Yoo KH, Sung KW, Kim SH. Kim IS, et al. Among authors: kim hj, kim sh. J Pediatr Hematol Oncol. 2006 Aug;28(8):540-3. doi: 10.1097/01.mph.0000212963.75630.93. J Pediatr Hematol Oncol. 2006. PMID: 16912597

8

Mutations in PRPS1, which encodes the phosphoribosyl pyrophosphate synthetase enzyme critical for nucleotide biosynthesis, cause hereditary peripheral neuropathy with hearing loss and optic neuropathy (cmtx5).

Kim HJ, Sohn KM, Shy ME, Krajewski KM, Hwang M, Park JH, Jang SY, Won HH, Choi BO, Hong SH, Kim BJ, Suh YL, Ki CS, Lee SY, Kim SH, Kim JW. Kim HJ, et al. Among authors: kim sh, kim bj, kim jw. Am J Hum Genet. 2007 Sep;81(3):552-8. doi: 10.1086/519529. Epub 2007 Jun 29. Am J Hum Genet. 2007. PMID: 17701900 Free PMC article.

9

Severe protein C deficiency from compound heterozygous mutations in the PROC gene in two Korean adult patients.

Kim HJ, Kim DK, Koh KC, Kim JY, Kim SH. Kim HJ, et al. Among authors: kim jy, kim sh, kim dk. Thromb Res. 2008;123(2):412-7. doi: 10.1016/j.thromres.2008.04.014. Epub 2008 Jun 24. Thromb Res. 2008. PMID: 18573519 No abstract available.

10

Is International Prognostic Scoring System (IPSS) still standard in predicting prognosis in patients with myelodysplastic syndrome? External validation of the WHO Classification-Based Prognostic Scoring System (WPSS) and comparison with IPSS.

Park MJ, Kim HJ, Kim SH, Kim DH, Kim SJ, Jang JH, Kim K, Kim WS, Jung CW. Park MJ, et al. Among authors: kim hj, kim dh, kim sh, kim sj, kim ws, kim k. Eur J Haematol. 2008 Nov;81(5):364-73. doi: 10.1111/j.1600-0609.2008.01124.x. Epub 2008 Jul 10. Eur J Haematol. 2008. PMID: 18637029

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