نتایج جستجو برای: myeloproliferative disorder

تعداد نتایج: 601334  

Myeloproliferative Neoplasm (MPN) are a clonal disorder in hematopoietic stem cells (HSC). MPN is categorized to 8 subclasses, including chronic myeloid leukemia (CML), polycythemia vera (PV), essential thrombocytopenia (ET), primary myelofibrosis (PMF), systematic mastositosis (SM), chronic eosinophilic leukemia (CEL), chronic neutrophilic leukemia (CNL), and unclassified myelofibrosis disorde...

Journal: :Indian Journal of Pathology and Microbiology 2012

Journal: :Haematologica 2013
Margarita Hurtado-Nedelec Marie-José Csillag-Grange Tarek Boussetta Sahra Amel Belambri Michèle Fay Bruno Cassinat Marie-Anne Gougerot-Pocidalo Pham My-Chan Dang Jamel El-Benna

Myeloproliferative disorders are associated with increased risk of thrombosis and vascular complications. The pathogenesis of these complications is not completely known. Reactive oxygen species produced by the neutrophil NADPH oxidase could have a role in this process. The aim of this study was to evaluate reactive oxygen species production by neutrophils of myeloproliferative disorder patient...

Journal: :The hematology journal : the official journal of the European Haematology Association 2004
José L Vizmanos Roberto Hernández María J Vidal María J Larráyoz María D Odero Julián Marín María T Ardanaz María J Calasanz Nicholas C P Cross

We report two new cases with the t(6;8)(q27;p12) and FGFR1OP-FGFR1 fusion. Case 1 presented with polycythaemia vera (PV) and evolved over 4 years to a myeloproliferative disorder (MPD) resembling the 8p11 myeloproliferative syndrome (EMS). Case 2 presented with B-cell lymphoblastic leukaemia (B-ALL). These cases illustrate the clinical heterogeneity observed in patients with FGFR1 rearrangement...

2018
Chunhong Liu Tao Yu Zhuo Xing Xiaoling Jiang Yichen Li Annie Pao Justin Mu Paul K. Wallace George Stoica Andrei V. Bakin Y. Eugene Yu

Individuals with Down syndrome (DS) frequently have hematopoietic abnormalities, including transient myeloproliferative disorder and acute megakaryoblastic leukemia which are often accompanied by acquired GATA1 mutations that produce a truncated protein, GATA1s. The mouse has been used for modeling DS based on the syntenic conservation between human chromosome 21 (Hsa21) and three regions in th...

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