MDS/MPN With SF3B1 Mutation and Thrombocytosis but Without Ring Sideroblasts
American Journal of Hematology, Volume 101, Issue 1, Page 129-130, January 2026.
Biswadip Hazarika, Barbara J. Bain
wiley +1 more source
Practical application and clinical impact of the WHO histopathological criteria on bone marrow biopsy for the diagnosis of essential thrombocythemia versus prefibrotic primary myelofibrosis [PDF]
, 2010 Aims: To evaluate the feasibility of the histopathological diagnosis of prefibrotic–early primary myelofibrosis (PM) as described in the World Health Organization (WHO) classification and to evaluate the clinical implications of prefibrotic–early PM in a
E. Parot-Schinkel +5 more
core +3 more sources
Comparison of Clinical and Hematological Parameters of Janus Kinase 2, Calreticulin or Myeloproliferative Leukemia Virus Oncogene Mutant Essential Thrombocythemia and Triple-Negative Essential Thrombocythemia [PDF]
, 2022 Jale Yıldız, Hikmettullah Batgi
openalex +1 more source
Blastic transformation of essential thrombocythemia: dual expression of myelomonoblastic/megakaryoblastic phenotypes [PDF]
, 1984 D Frei-Lahr +4 more
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Haematologica, 2009 To observe the effect of the new World Health Organization (WHO) criteria on the incidence of myeloproliferative neoplasms, we performed a retrospective study of a population-based registry in the Côte d’Or area, France, from 1980 to 2007. A total of 524
François Girodon +9 more
doaj +1 more source
Incidence of venous thromboembolism and use of anticoagulation in hematological malignancies: Critical review of the literature [PDF]
, 2018 Venous Thromboembolism (VTE) frequently complicates the course of hematologic malignancies (HM) and its incidence is similar to that observed in high-risk solid tumors.
Annibali, Ombretta +3 more
core +2 more sources
Moyamoya syndrome in an adult with essential thrombocythemia
Neurology International, 2011 Moyamoya syndrome is a rare cerebrovascular disorder characterized by progressive occlusion of the supraclinoid internal carotid artery and proximal portions of the anterior and middle cerebral arteries resulting in an extensive network of collateralized
Marc Lazzaro +3 more
doaj +1 more source
Cytogenetics, JAK2 and MPL mutations in polycythemia vera, primary myelofibrosis and essential thrombocythemia [PDF]
, 2011 BACKGROUND: The detection of molecular and cytogenetic alterations is important for the diagnosis, prognosis and classification of myeloproliferative neoplasms. OBJECTIVE: The aim of this study was to detect the following mutations: JAK2 V617F, JAK2 exon
Cerutti, Janete Maria +5 more
core +3 more sources
Haematologica, 2010 Primary myelofibrosis shows histological and pathogenetic overlap with essential thrombocythemia and polycythemia vera. Several diagnostic classifications have been proposed for primary myelofibrosis, although little is known about their clinical utility.
Philip A. Beer +2 more
doaj +1 more source