Kim H - Search Results

1

Genome-wide single-nucleotide polymorphism array-based karyotyping in myelodysplastic syndrome and chronic myelomonocytic leukemia and its impact on treatment outcomes following decitabine treatment.

Yi JH, Huh J, Kim HJ, Kim SH, Kim SH, Kim KH, Do YR, Mun YC, Kim H, Kim MK, Kim HJ, Kim T, Kim DD. Yi JH, et al. Among authors: kim dd, kim h, kim hj, kim sh, kim t, kim kh, kim mk. Ann Hematol. 2013 Apr;92(4):459-69. doi: 10.1007/s00277-012-1635-7. Epub 2012 Dec 23. Ann Hematol. 2013. PMID: 23262795

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

6

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. 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

7

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. 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.

8

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. 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.

9

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. 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

10

Screening of subtelomeric rearrangements in 100 Korean Pediatric patients with unexplained mental retardation and anomalies using subtelomeric FISH (fluorescence in situ hybridization).

Park HK, Kim HJ, Kim HJ, Han SH, Kim YJ, Kim SH. Park HK, et al. J Korean Med Sci. 2008 Aug;23(4):573-8. doi: 10.3346/jkms.2008.23.4.573. J Korean Med Sci. 2008. PMID: 18756040 Free PMC article.

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