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Keywords: Essential thrombocythaemiaClose
Acta Haematol (2021) 144 (3): 337–344.
Published Online: 23 November 2020
...Kyung Chul Moon; Jeong-An Gim; Dae Sik Kim; Chul Won Choi; Jung Yoon; Soo-Young Yoon Differentiating the aetiology of thrombocytosis is limited yet crucial in patients with essential thrombocythaemia (ET). MicroRNAs (miRNAs) regulate haematopoiesis and lineage commitment; aberrant expression...
Elena Tirrò, Stefania Stella, Michele Massimino, Valentina Zammit, Maria Stella Pennisi, Silvia Rita Vitale, Chiara Romano, Sandra Di Gregorio, Adriana Puma, Francesco Di Raimondo, Fabio Stagno, Livia Manzella
Acta Haematol (2019) 141 (4): 261–267.
Published Online: 09 April 2019
.... Essential thrombocythaemia Chronic myeloid leukaemia JAK2 V617F BCR-ABL1 Myeloproliferative disorders (MPDs) are chronic haematological malignancies characterised by the clonal expansion of a transformed haematopoietic stem cell. Detection of a balanced translocation involving the long arms...
Acta Haematol (2018) 140 (4): 234–239.
Published Online: 07 November 2018
...Achille Pich; Ludovica Riera; Paola Francia di Celle; Eloise Beggiato; Giulia Benevolo; Laura Godio Introduction: Mutations in the JAK2 , CALR , and MPL genes have been shown to have prognostic value in essential thrombocythaemia (ET), but no clear association with morphological changes has been...
Acta Haematol (1985) 73 (4): 219–223.
Published Online: 25 February 2009
...F. Waweru; S.M. Lewis Essential thrombocythaemia was diagnosed in a series of 18 patients on the basis of platelet counts greater than 1,000 × 10 9 /1. Radionuclide studies have been carried out to distinguish thrombocythaemia as a primary disease from polycythaemia vera, myelofibrosis and chronic...
Acta Haematol (1989) 82 (3): 150–153.
Published Online: 20 February 2009
...Nicola Lucio Liberato; Giovanni Barosi; Attilia Costa; Paola D’Elia; Piero Boccaccio We report a male patient in whom a diagnosis of essential thrombocythaemia was made at the age of 25. The clinical course was characterised by recurrent thrombotic episodes during the first few years of the disease...
Acta Haematol (1990) 83 (4): 203–205.
Published Online: 20 February 2009
...P.J. Browett; H.E. Heslop; A.B. Mehta; J.D. Norton A 42-year-old woman presented with clinical and haematological features of essential thrombocythaemia (ET). Cytogenetic investigation revealed a standard t(9;22) Philadelphia translocation in all evaluable metaphases which persisted throughout...
Acta Haematol (1994) 91 (3): 126–129.
Published Online: 18 February 2009
...V. Rametta; F. Ferrara; V. Marottoli; C. Matera; V. Mettivier; R. Cimino We report the disease characteristics and therapeutic results for 25 patient suffering from essential thrombocythaemia (ET), treated with recombinant in terferon-alpha-2b (IFN-α2b). ET was diagnosed according...
Acta Haematol (1996) 96 (4): 227–231.
Published Online: 17 February 2009
...Riitta Jantunen; Eeva Juvonen; Ari Aimolahti; Tapani Ruutu Bone marrow samples of 8 patients with essential thrombocythaemia and three patients with polycythaemia vera were cultured in long-term bone marrow cultures. The production of non-adherent cells and colony-forming unit-granulocyte...
Acta Haematol (2001) 106 (3): 122–125.
Published Online: 16 November 2001
... at the level of the colony-forming unit granulocytes, erythrocytes, macrophages, megakaryocytes. No cytogenetic abnormalities were observed. The criteria which have been proposed to differentiate essential thrombocythaemia from pre-fibrotic thrombocythaemia, as an early phase of idiopathic myelofibrosis...