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本文引用的文献

1
Application of current prognostic models for primary myelofibrosis in the setting of post-polycythemia vera or post-essential thrombocythemia myelofibrosis.当前原发性骨髓纤维化预后模型在真性红细胞增多症后或原发性血小板增多症后骨髓纤维化中的应用。
Leukemia. 2017 Dec;31(12):2851-2852. doi: 10.1038/leu.2017.268. Epub 2017 Aug 18.
2
Cytogenetic findings in WHO-defined polycythaemia vera and their prognostic relevance.世界卫生组织定义的真性红细胞增多症的细胞遗传学发现及其预后相关性。
Br J Haematol. 2018 Aug;182(3):437-440. doi: 10.1111/bjh.14798. Epub 2017 Jun 9.
3
Patients with post-essential thrombocythemia and post-polycythemia vera differ from patients with primary myelofibrosis.原发性血小板增多症后和真性红细胞增多症后的患者与原发性骨髓纤维化患者有所不同。
Leuk Res. 2017 Aug;59:110-116. doi: 10.1016/j.leukres.2017.06.001. Epub 2017 Jun 2.
4
A clinical-molecular prognostic model to predict survival in patients with post polycythemia vera and post essential thrombocythemia myelofibrosis.一个临床-分子预后模型,用于预测真性红细胞增多症后和特发性血小板增多症后骨髓纤维化患者的生存情况。
Leukemia. 2017 Dec;31(12):2726-2731. doi: 10.1038/leu.2017.169. Epub 2017 May 31.
5
Characteristics and clinical significance of cytogenetic abnormalities in polycythemia vera.原发性骨髓纤维化中细胞遗传学异常的特征和临床意义。
Haematologica. 2017 Sep;102(9):1511-1518. doi: 10.3324/haematol.2017.165795. Epub 2017 May 4.
6
Update from the latest WHO classification of MPNs: a user's manual.世界卫生组织髓系增殖性肿瘤最新分类更新:用户指南。
Hematology Am Soc Hematol Educ Program. 2016 Dec 2;2016(1):534-542. doi: 10.1182/asheducation-2016.1.534.
7
Driver mutations' effect in secondary myelofibrosis: an international multicenter study based on 781 patients.驱动突变在继发性骨髓纤维化中的作用:一项基于781例患者的国际多中心研究。
Leukemia. 2017 Apr;31(4):970-973. doi: 10.1038/leu.2016.351. Epub 2016 Nov 25.
8
A compendium of cytogenetic abnormalities in myelofibrosis: molecular and phenotypic correlates in 826 patients.骨髓纤维化细胞遗传学异常简编:826例患者的分子与表型相关性
Br J Haematol. 2015 Apr;169(1):71-6. doi: 10.1111/bjh.13260. Epub 2014 Dec 17.
9
Initial bone marrow reticulin fibrosis in polycythemia vera exerts an impact on clinical outcome.原发性骨髓纤维化在真性红细胞增多症中产生影响。
Blood. 2012 Mar 8;119(10):2239-41. doi: 10.1182/blood-2011-11-393819. Epub 2012 Jan 13.
10
The role of the JAK2 GGCC haplotype and the TET2 gene in familial myeloproliferative neoplasms.JAK2 GGCC 单倍型和 TET2 基因在家族性骨髓增殖性肿瘤中的作用。
Haematologica. 2011 Mar;96(3):367-74. doi: 10.3324/haematol.2010.034488. Epub 2010 Dec 20.

Value of cytogenetic abnormalities in post-polycythemia vera and post-essential thrombocythemia myelofibrosis: a study of the MYSEC project.

作者信息

Mora Barbara, Giorgino Toni, Guglielmelli Paola, Rumi Elisa, Maffioli Margherita, Rambaldi Alessandro, Caramella Marianna, Komrokji Rami, Gotlib Jason, Kiladjian Jean Jacques, Cervantes Francisco, Devos Timothy, Palandri Francesca, De Stefano Valerio, Ruggeri Marco, Silver Richard T, Benevolo Giulia, Albano Francesco, Cavalloni Chiara, Barraco Daniela, Merli Michele, Pietra Daniela, Casalone Rosario, Barbui Tiziano, Rotunno Giada, Cazzola Mario, Vannucchi Alessandro Maria, Passamonti Francesco

机构信息

Hematology, Department of Medicine and Surgery, University of Insubria, Ospedale di Circolo, ASST Sette Laghi, Varese, Italy.

Biophysics Institute, National Research Council of Italy, Milano, Italy.

出版信息

Haematologica. 2018 Sep;103(9):e392-e394. doi: 10.3324/haematol.2017.185751. Epub 2018 Apr 5.

DOI:10.3324/haematol.2017.185751
PMID:
29622658
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6119135/
Abstract
摘要