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5. Molecular correlates of anemia in primary myelofibrosis: a significant and independent association with U2AF1 mutations. Barraco D; Elala YC; Lasho TL; Begna KH; Gangat N; Finke C; Hanson CA; Ketterling RP; Pardanani A; Tefferi A Blood Cancer J; 2016 Apr; 6(4):e415. PubMed ID: 27058230 [No Abstract] [Full Text] [Related]
6. An unusual long-term outcome of a child with primary myelofibrosis harboring a JAK2 mutation. Maia RC; Bonamino MH; Robaina MC; Amaral N; Bonecker S; Zalcberg IR; Klumb CE Blood Cells Mol Dis; 2015 Dec; 55(4):347-50. PubMed ID: 26460258 [TBL] [Abstract][Full Text] [Related]
7. Co-existence of JAK2 V617F and CALR mutations in primary myelofibrosis. Zamora L; Xicoy B; Cabezón M; Fernandez C; Marcé S; Velez P; Xandri M; Gallardo D; Millá F; Feliu E; Boqué C Leuk Lymphoma; 2015; 56(10):2973-4. PubMed ID: 25686645 [No Abstract] [Full Text] [Related]
8. Prognosis and survivorship in primary myelofibrosis. Reilly JT Am J Hematol; 2010 Jan; 85(1):4-5. PubMed ID: 20029947 [No Abstract] [Full Text] [Related]
9. The lack of association between JAK2 V617F mutation and myelodysplastic syndrome with or without myelofibrosis. Yip SF; So CC; Chan AY; Liu HY; Wan TsK; Chan LC Leukemia; 2006 Jun; 20(6):1165. PubMed ID: 16572200 [No Abstract] [Full Text] [Related]
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11. CALR-mutated primary myelofibrosis evolving to chronic myeloid leukemia with both CALR mutation and BCR-ABL1 fusion gene. Diamond JM; de Almeida AM; Belo HJ; da Costa MP; Cabeçadas JM; Abecasis MM Ann Hematol; 2016 Dec; 95(12):2101-2104. PubMed ID: 27699446 [No Abstract] [Full Text] [Related]
12. The impact of cytogenetic abnormalities on the prognosis of primary myelofibrosis: a prospective survey of 202 cases in Japan. Hidaka T; Shide K; Shimoda H; Kameda T; Toyama K; Katayose K; Kubuki Y; Nagata K; Takenaka K; Akashi K; Okamura T; Niho Y; Mizoguchi H; Omine M; Ozawa K; Harada M; Shimoda K Eur J Haematol; 2009 Oct; 83(4):328-33. PubMed ID: 19549278 [TBL] [Abstract][Full Text] [Related]
13. Prognostic relevance of cytogenetic abnormalities in primary myelofibrosis: comparison of recent reports from Japan, the Mayo Clinic and MD Anderson Cancer Center. Tefferi A Eur J Haematol; 2009 Oct; 83(4):290-1. PubMed ID: 19558507 [No Abstract] [Full Text] [Related]
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15. Prognosis of Primary Myelofibrosis in the Genomic Era. Bose P; Verstovsek S Clin Lymphoma Myeloma Leuk; 2016 Aug; 16 Suppl():S105-13. PubMed ID: 27521306 [TBL] [Abstract][Full Text] [Related]
16. MPL mutations and palpable splenomegaly are independent risk factors for fibrotic progression in essential thrombocythemia. Haider M; Elala YC; Gangat N; Hanson CA; Tefferi A Blood Cancer J; 2016 Oct; 6(10):e487. PubMed ID: 27768091 [No Abstract] [Full Text] [Related]
17. Improved survival in patients with CALR1 compared to CALR2 mutated primary myelofibrosis: a meta-analysis. Kourie HR; Ameye L; Paesmans M; Bron D Br J Haematol; 2017 Dec; 179(5):846-848. PubMed ID: 27434541 [No Abstract] [Full Text] [Related]
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20. MIPSS70+ Version 2.0: Mutation and Karyotype-Enhanced International Prognostic Scoring System for Primary Myelofibrosis. Tefferi A; Guglielmelli P; Lasho TL; Gangat N; Ketterling RP; Pardanani A; Vannucchi AM J Clin Oncol; 2018 Jun; 36(17):1769-1770. PubMed ID: 29708808 [No Abstract] [Full Text] [Related] [Next] [New Search]