Hunger SP - Search Results

1

Philadelphia chromosome-negative very high-risk acute lymphoblastic leukemia in children and adolescents: results from Children's Oncology Group Study AALL0031.

Schultz KR, Devidas M, Bowman WP, Aledo A, Slayton WB, Sather H, Zheng HW, Davies SM, Gaynon PS, Trigg M, Rutledge R, Jorstad D, Carroll AJ, Heerema N, Winick N, Borowitz MJ, Hunger SP, Carroll WL, Camitta B; Children’s Oncology Group. Schultz KR, et al. Among authors: hunger sp. Leukemia. 2014 Apr;28(4):964-7. doi: 10.1038/leu.2014.29. Epub 2014 Jan 17. Leukemia. 2014. PMID: 24434862 Free PMC article. No abstract available.

2

The t(1;19)(q23;p13) results in consistent fusion of E2A and PBX1 coding sequences in acute lymphoblastic leukemias.

Hunger SP, Galili N, Carroll AJ, Crist WM, Link MP, Cleary ML. Hunger SP, et al. Blood. 1991 Feb 15;77(4):687-93. Blood. 1991. PMID: 1671560 Free article.

3

Consistent involvement of the bcr gene by 9;22 breakpoints in pediatric acute leukemias.

Suryanarayan K, Hunger SP, Kohler S, Carroll AJ, Crist W, Link MP, Cleary ML. Suryanarayan K, et al. Among authors: hunger sp. Blood. 1991 Jan 15;77(2):324-30. Blood. 1991. PMID: 1985699 Free article.

4

Predictability of the t(1;19)(q23;p13) from surface antigen phenotype: implications for screening cases of childhood acute lymphoblastic leukemia for molecular analysis: a Pediatric Oncology Group study.

Borowitz MJ, Hunger SP, Carroll AJ, Shuster JJ, Pullen DJ, Steuber CP, Cleary ML. Borowitz MJ, et al. Among authors: hunger sp. Blood. 1993 Aug 15;82(4):1086-91. Blood. 1993. PMID: 8353275 Free article.

5

HRX involvement in de novo and secondary leukemias with diverse chromosome 11q23 abnormalities.

Hunger SP, Tkachuk DC, Amylon MD, Link MP, Carroll AJ, Welborn JL, Willman CL, Cleary ML. Hunger SP, et al. Blood. 1993 Jun 15;81(12):3197-203. Blood. 1993. PMID: 8389614 Free article.

6

Lack of ETV6 (TEL) gene rearrangements or p16INK4A/p15INK4B homozygous gene deletions in infant acute lymphoblastic leukemia.

Maloney KW, Rubnitz JE, Cleary ML, Frankel LS, Hakami N, Link MP, Pullen DJ, Hunger SP. Maloney KW, et al. Among authors: hunger sp. Leukemia. 1997 Jul;11(7):979-83. doi: 10.1038/sj.leu.2400687. Leukemia. 1997. PMID: 9204978

7

Hyperdiploidy and E2A-PBX1 fusion in an adult with t(1;19)+ acute lymphoblastic leukemia: case report and review of the literature.

Hunger SP, Sun T, Boswell AF, Carroll AJ, McGavran L. Hunger SP, et al. Genes Chromosomes Cancer. 1997 Dec;20(4):392-8. doi: 10.1002/(sici)1098-2264(199712)20:4<392::aid-gcc11>3.0.co;2-p. Genes Chromosomes Cancer. 1997. PMID: 9408756 Review.

8

E2A-PBX1 chimeric transcript status at end of consolidation is not predictive of treatment outcome in childhood acute lymphoblastic leukemias with a t(1;19)(q23;p13): a Pediatric Oncology Group study.

Hunger SP, Fall MZ, Camitta BM, Carroll AJ, Link MP, Lauer SJ, Mahoney DH, Pullen DJ, Shuster JJ, Steuber CP, Cleary ML. Hunger SP, et al. Blood. 1998 Feb 1;91(3):1021-8. Blood. 1998. PMID: 9446665 Free article. Clinical Trial.

9

Different patterns of homozygous p16INK4A and p15INK4B deletions in childhood acute lymphoblastic leukemias containing distinct E2A translocations.

Maloney KW, McGavran L, Odom LF, Hunger SP. Maloney KW, et al. Among authors: hunger sp. Leukemia. 1998 Sep;12(9):1417-21. doi: 10.1038/sj.leu.2401124. Leukemia. 1998. PMID: 9737691

10

TEL-AML1 fusion identifies a subset of children with standard risk acute lymphoblastic leukemia who have an excellent prognosis when treated with therapy that includes a single delayed intensification.

Maloney K, McGavran L, Murphy J, Odom L, Stork L, Wei Q, Hunger S. Maloney K, et al. Leukemia. 1999 Nov;13(11):1708-12. doi: 10.1038/sj.leu.2401548. Leukemia. 1999. PMID: 10557042

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