The outcome of allo-HSCT for 92 patients with myelofibrosis in the Nordic countries-Reference-Cited by-同舟云学术

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The outcome of allo-HSCT for 92 patients with myelofibrosis in the Nordic countries

Published:2011-05-09 Issue:3 Volume:47 Page:380-386
ISSN:0268-3369
Container-title:Bone Marrow Transplantation
language:en
Short-container-title:Bone Marrow Transplant

Author:

Abelsson J, ,Merup M,Birgegård G,WeisBjerrum O,Brinch L,Brune M,Johansson P,Kauppila M,Lenhoff S,Liljeholm M,Malm C,Remes K,Vindelöv L,Andréasson B

Publisher

Springer Science and Business Media LLC

Subject

Transplantation,Hematology

Link

http://www.nature.com/articles/bmt201191.pdf

Reference22 articles.

1. Tefferi A, Gangat N, Wolanskyj AP, Schwager S, Pardanani A, Lasho TL et al. 20+ yr without leukemic or fibrotic transformation in essential thrombocythemia or polycythemia vera: predictors at diagnosis. Eur J Haematol 2008; 80: 386–390.

2. Kralovics R, Passamonti F, Buser AS, Teo SS, Tiedt R, Passweg JR et al. A gain-of-function mutation of JAK2 in myeloproliferative disorders. N Engl J Med 2005; 352: 1779–1790.

3. Passamonti F, Rumi E, Pungolino E, Malabarba L, Bertazzoni P, Valentini M et al. Life expectancy and prognostic factors for survival in patients with polycythemia vera and essential thrombocythemia. Am J Med 2004; 117: 755–761.

4. Thiele J, Kvasnicka HM . Clinicopathological criteria for differential diagnosis of thrombocythemias in various myeloproliferative disorders. Semin Thromb Hemost 2006; 32: 219–230.

5. Barosi G . Myelofibrosis with myeloid metaplasia: diagnostic definition and prognostic classification for clinical studies and treatment guidelines. J Clin Oncol 1999; 17: 2954–2970.

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