Koo HH - Search Results

1

Recurrent somatic mutations and low germline predisposition mutations in Korean ALL patients.

Shin SY, Lee H, Lee ST, Choi JR, Jung CW, Koo HH, Kim SH. Shin SY, et al. Among authors: koo hh. Sci Rep. 2021 Apr 26;11(1):8893. doi: 10.1038/s41598-021-88449-4. Sci Rep. 2021. PMID: 33903686 Free PMC article. 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: koo hh. 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: koo hh. Am J Hematol. 2004 Aug;76(4):360-3. doi: 10.1002/ajh.20117. Am J Hematol. 2004. PMID: 15282669 Free article.

4

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

5

Clinicopathologic features and treatment outcomes in malignant lymphoma of pediatric and young adult patients in Korea: comparison of korean all-ages group and Western younger age group.

Hwang IG, Yoo KH, Lee SH, Park YH, Lim TK, Lee SC, Park S, Park BB, Ko YH, Kim K, Koo HH, Kim WS. Hwang IG, et al. Among authors: koo hh. Clin Lymphoma Myeloma. 2007 Nov;7(9):580-6. doi: 10.3816/clm.2007.n.044. Clin Lymphoma Myeloma. 2007. PMID: 18186966

6

A novel four-way t(6;16;21;8)(p21.3;p11.2;q22;q22) in acute myeloid leukemia with RUNX1/RUNX1T1 rearrangement.

Park KJ, Park HD, Kim HJ, Yoo KH, Koo HH, Kim SH. Park KJ, et al. Among authors: koo hh. Cancer Genet Cytogenet. 2009 Jul 15;192(2):90-2. doi: 10.1016/j.cancergencyto.2009.03.013. Cancer Genet Cytogenet. 2009. PMID: 19596262 No abstract available.

7

UNC13D is the predominant causative gene with recurrent splicing mutations in Korean patients with familial hemophagocytic lymphohistiocytosis.

Yoon HS, Kim HJ, Yoo KH, Sung KW, Koo HH, Kang HJ, Shin HY, Ahn HS, Kim JY, Lim YT, Bae KW, Lee KO, Shin JS, Lee ST, Chung HS, Kim SH, Park CJ, Chi HS, Im HJ, Seo JJ. Yoon HS, et al. Among authors: koo hh. Haematologica. 2010 Apr;95(4):622-6. doi: 10.3324/haematol.2009.016949. Epub 2009 Dec 16. Haematologica. 2010. PMID: 20015888 Free PMC article.

8

Measurement of tyrosine hydroxylase transcripts in bone marrow using biopsied tissue instead of aspirates for neuroblastoma.

Lee ST, Suh YL, Ko YH, Ki CS, Sung KW, Kim HJ, Kim JW, Kim SH, Chueh H, Lee SH, Yoo KH, Koo HH. Lee ST, et al. Among authors: koo hh. Pediatr Blood Cancer. 2010 Aug;55(2):273-8. doi: 10.1002/pbc.22483. Pediatr Blood Cancer. 2010. PMID: 20582938

9

Molecular detection of tyrosine hydroxylase in the peripheral blood of patients with neuroblastoma: useful at diagnosis but not predictive of subsequent relapse during off-therapy follow-up.

Lee ST, Ki CS, Sung KW, Kim HJ, Kim JW, Kim SH, Lee SH, Yoo KH, Koo HH, Kim JY, Cho EJ. Lee ST, et al. Among authors: koo hh. Pediatr Hematol Oncol. 2011 Feb;28(1):16-23. doi: 10.3109/08880018.2010.514694. Epub 2010 Nov 17. Pediatr Hematol Oncol. 2011. PMID: 21083359

10

Acute myeloid leukemia with complex hypodiploidy and loss of heterozygosity of 17p in a boy with Fanconi anemia.

Woo HI, Kim HJ, Lee SH, Yoo KH, Koo HH, Kim SH. Woo HI, et al. Among authors: koo hh. Ann Clin Lab Sci. 2011 Fall;41(1):66-70. Ann Clin Lab Sci. 2011. PMID: 21325258

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