Results 171 to 180 of about 28,502 (229)
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BMJ, 2019
Thrombocytosis is defined as a platelet count elevated more than two standard deviations above the population mean, typically >400-450×10/L, and therefore includes 2.3% of the population.
Abhinav, Mathur +3 more
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Thrombocytosis is defined as a platelet count elevated more than two standard deviations above the population mean, typically >400-450×10/L, and therefore includes 2.3% of the population.
Abhinav, Mathur +3 more
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Ring sideroblasts (RS) are erythroid precursors with abnormal perinuclear mitochondrial iron accumulation. Two myeloid neoplasms defined by the presence of RS, include refractory anemia with ring sideroblasts (RARS), now classified under myelodysplastic ...
M S Patnaik, Ayalew Tefferi
exaly +2 more sources
British Journal of Haematology, 1995
Four cases of thrombocytosis in three successive generations of a family are described. High peripheral platelet count was found incidentally in the proband with cutaneous malignant lymphoma. Bone marrow examination showed megakaryocytic hyperplasia. Neither Philadephia chromosome nor chimaeric bcr/abl junction was detected in marrow cells.
M, Kikuchi +5 more
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Four cases of thrombocytosis in three successive generations of a family are described. High peripheral platelet count was found incidentally in the proband with cutaneous malignant lymphoma. Bone marrow examination showed megakaryocytic hyperplasia. Neither Philadephia chromosome nor chimaeric bcr/abl junction was detected in marrow cells.
M, Kikuchi +5 more
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How useful is thrombocytosis in predicting an underlying cancer in primary care? a systematic review
Sarah E R Bailey +2 more
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Hematology, 2007
Abstract The aim of this review is to discuss current diagnostic approaches to, and classification of, patients presenting with thrombocytosis, in light of novel information derived from the discovery of specific molecular abnormalities in chronic myeloproliferative disorders (CMPD), which represent the most common cause of primary ...
VANNUCCHI, ALESSANDRO MARIA, Barbui T.
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Abstract The aim of this review is to discuss current diagnostic approaches to, and classification of, patients presenting with thrombocytosis, in light of novel information derived from the discovery of specific molecular abnormalities in chronic myeloproliferative disorders (CMPD), which represent the most common cause of primary ...
VANNUCCHI, ALESSANDRO MARIA, Barbui T.
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Hematology, 2009
AbstractMajor progress in understanding the pathogenesis in patients with thrombocytosis has been made by identifying mutations in the key regulators of thrombopoietin: the thrombopoietin receptor MPL and JAK2. Together, these mutations can be found in 50% to 60% of patients with essential thrombocythemia or primary myelofibrosis and in 10% to 20% of ...
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AbstractMajor progress in understanding the pathogenesis in patients with thrombocytosis has been made by identifying mutations in the key regulators of thrombopoietin: the thrombopoietin receptor MPL and JAK2. Together, these mutations can be found in 50% to 60% of patients with essential thrombocythemia or primary myelofibrosis and in 10% to 20% of ...
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Acta Medica Scandinavica, 1973
Abstract The numbers of circulating platelets have been determined in a series comprising 4 003 hospitalized patients. An elevated platelet count (> 400 000/μl) was found in 222 cases. Frequency figures of thrombocytosis in excess of 30% found in myeloproliferative disorders, amyloidosis, ulcerative colitis, rheumatoid arthritis, ankylosing ...
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Abstract The numbers of circulating platelets have been determined in a series comprising 4 003 hospitalized patients. An elevated platelet count (> 400 000/μl) was found in 222 cases. Frequency figures of thrombocytosis in excess of 30% found in myeloproliferative disorders, amyloidosis, ulcerative colitis, rheumatoid arthritis, ankylosing ...
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Reactive thrombocytosis in acute infectious diseases: Prevalence, characteristics and timing.
European journal of internal medicine, 2019BACKGROUND Reactive thrombocytosis is known to occur in infectious, inflammatory and neoplastic diseases. However, the characteristics of its association with acute infections (ID) has not been systematically studied.
A. Schattner, J. Kadi, I. Dubin
semanticscholar +1 more source
2018
Abstract This chapter guides the reader on the diagnosis and management of thrombocytosis in hospitalized patients.
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Abstract This chapter guides the reader on the diagnosis and management of thrombocytosis in hospitalized patients.
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Benign familial thrombocytosis
American Journal of Hematology, 1991AbstractA 13‐year‐old girl was found to have a platelet count in excess of 4 million/μl while being evaluated for a minor bleeding episode. Her father and two sisters also had thrombocytosis. All four affected patients were asymptomatic and had no clinical or laboratory evidence of a myeloproliferative disorder other than an elevated platelet count ...
E C, Williams, N T, Shahidi
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