Kim HJ - Search Results

1

A case of CD5-positive mature B-cell neoplasm with t(10;14)(q24;q11.2) and trisomy 12.

Shin SY, Lee ST, Kim HJ, Jang JH, Jung CW, Kim SH. Shin SY, et al. Among authors: kim hj, kim sh. Leuk Lymphoma. 2015 May;56(5):1550-1. doi: 10.3109/10428194.2014.971408. Epub 2014 Nov 3. Leuk Lymphoma. 2015. PMID: 25284493 No abstract available.

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

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.

5

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

6

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.

7

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.

8

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

9

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. Among authors: kim yj, kim hj, kim sh. 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.

10

Severe factor XI deficiency in a Korean woman with a novel missense mutation (Val498Met) and duplication G mutation in exon 13 of the F11 gene.

Kwon MJ, Kim HJ, Bang SH, Kim SH. Kwon MJ, et al. Among authors: kim hj, kim sh. Blood Coagul Fibrinolysis. 2008 Oct;19(7):679-83. doi: 10.1097/MBC.0b013e32830ef8f9. Blood Coagul Fibrinolysis. 2008. PMID: 18832909

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