Hanson CA - Search Results

1

BCR-JAK2 fusion in a myeloproliferative neoplasm with associated eosinophilia.

He R, Greipp PT, Rangan A, Mai M, Chen D, Reichard KK, Nelsen LL, Pardanani A, Hanson CA, Viswanatha DS. He R, et al. Among authors: hanson ca. Cancer Genet. 2016 May;209(5):223-8. doi: 10.1016/j.cancergen.2016.03.002. Epub 2016 Apr 6. Cancer Genet. 2016. PMID: 27134074

2

Clinical correlations of immunophenotypic variations and the presence of trisomy 12 in B-cell chronic lymphocytic leukemia.

Tefferi A, Bartholmai BJ, Witzig TE, Jenkins RB, Li CY, Hanson CA, Mesa RA, Phyliky RL. Tefferi A, et al. Among authors: hanson ca. Cancer Genet Cytogenet. 1997 Jun;95(2):173-7. doi: 10.1016/s0165-4608(96)00249-x. Cancer Genet Cytogenet. 1997. PMID: 9169037 Review.

3

A novel three-color, clone-specific fluorescence in situ hybridization procedure for monoclonal gammopathies.

Ahmann GJ, Jalal SM, Juneau AL, Christensen ER, Hanson CA, Dewald GW, Greipp PR. Ahmann GJ, et al. Among authors: hanson ca. Cancer Genet Cytogenet. 1998 Feb;101(1):7-11. doi: 10.1016/s0165-4608(97)00058-7. Cancer Genet Cytogenet. 1998. PMID: 9460493

4

Detection of RB1 deletions by fluorescence in situ hybridization in malignant hematologic disorders.

Juneau AL, Kaehler M, Christensen ER, Schad CR, Zinsmeister AR, Lust J, Hanson C, Dewald GW. Juneau AL, et al. Cancer Genet Cytogenet. 1998 Jun;103(2):117-23. doi: 10.1016/s0165-4608(97)00408-1. Cancer Genet Cytogenet. 1998. PMID: 9614909

5

Isolated isochromosome 17q: a distinct type of mixed myeloproliferative disorder/myelodysplastic syndrome with an aggressive clinical course.

McClure RF, Dewald GW, Hoyer JD, Hanson CA. McClure RF, et al. Among authors: hanson ca. Br J Haematol. 1999 Aug;106(2):445-54. doi: 10.1046/j.1365-2141.1999.01537.x. Br J Haematol. 1999. PMID: 10460605 Free article.

6

Phase 2 trial of imatinib mesylate in myelofibrosis with myeloid metaplasia.

Tefferi A, Mesa RA, Gray LA, Steensma DP, Camoriano JK, Elliott MA, Pardanani A, Ansell SM, Call TG, Colon-Otero G, Schroeder G, Hanson CA, Dewald GW, Kaufmann SH. Tefferi A, et al. Among authors: hanson ca. Blood. 2002 May 15;99(10):3854-6. doi: 10.1182/blood-2001-12-0154. Blood. 2002. PMID: 11986248 Free article. Clinical Trial.

7

Frequency, hematopathology, and detection of a new isodicentric variant of deletion 20q.

Smoley SA, Fink SR, Paternoster SF, Stockero KJ, Nguyen LP, Nguyen PL, Hanson CA, Dewald GW. Smoley SA, et al. Among authors: hanson ca. Cancer Genet Cytogenet. 2007 Mar;173(2):144-9. doi: 10.1016/j.cancergencyto.2006.11.003. Cancer Genet Cytogenet. 2007. PMID: 17321330

8

Prevalence and clinicopathologic correlates of JAK2 exon 12 mutations in JAK2V617F-negative polycythemia vera.

Pardanani A, Lasho TL, Finke C, Hanson CA, Tefferi A. Pardanani A, et al. Among authors: hanson ca. Leukemia. 2007 Sep;21(9):1960-3. doi: 10.1038/sj.leu.2404810. Epub 2007 Jun 28. Leukemia. 2007. PMID: 17597810

9

Low JAK2V617F allele burden in primary myelofibrosis, compared to either a higher allele burden or unmutated status, is associated with inferior overall and leukemia-free survival.

Tefferi A, Lasho TL, Huang J, Finke C, Mesa RA, Li CY, Wu W, Hanson CA, Pardanani A. Tefferi A, et al. Among authors: hanson ca. Leukemia. 2008 Apr;22(4):756-61. doi: 10.1038/sj.leu.2405097. Epub 2008 Jan 24. Leukemia. 2008. PMID: 18216871

10

20+ yr without leukemic or fibrotic transformation in essential thrombocythemia or polycythemia vera: predictors at diagnosis.

Tefferi A, Gangat N, Wolanskyj AP, Schwager S, Pardanani A, Lasho TL, Mesa R, McClure RF, Li CY, Hanson CA. Tefferi A, et al. Among authors: hanson ca. Eur J Haematol. 2008 May;80(5):386-90. doi: 10.1111/j.1600-0609.2008.01038.x. Epub 2008 Jan 23. Eur J Haematol. 2008. PMID: 18221390

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