Results 301 to 310 of about 283,642 (353)
[Myeloproliferative disorders and blood platelet function].
Hideaki Uchino
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Treatment of disorders of blood platelets.
Jackson Dp
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American Journal of Clinical Pathology, 1991
In vitro platelet aggregation in platelet-rich plasma (PRP) and in whole blood (WB) was assessed in 31 patients with idiopathic myelofibrosis, 32 with essential thrombocytosis, 23 with polycythemia vera, and 34 with chronic myelogenous leukemia. In PRP most subjects showed normal or reduced platelet aggregation, whereas in WB the majority of patients ...
BALDUINI, CARLO +3 more
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In vitro platelet aggregation in platelet-rich plasma (PRP) and in whole blood (WB) was assessed in 31 patients with idiopathic myelofibrosis, 32 with essential thrombocytosis, 23 with polycythemia vera, and 34 with chronic myelogenous leukemia. In PRP most subjects showed normal or reduced platelet aggregation, whereas in WB the majority of patients ...
BALDUINI, CARLO +3 more
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Blood platelet and "extra-platelet" serotonin in some myeloproliferative disorders.
Biomedicine / [publiee pour l'A.A.I.C.I.G.], 1978Most of the blood serotonin is bound to platelets. However, some authors described plasma "free" serotonin; which is normally very low, and might be increased during some diseases. Usual spectrofluorimetric methods and paired by statistical evaluation "extra-platelet" serotonin (not bound to platelets) in the blood of healthy volunteers and patients ...
J M, Culebras Poza +3 more
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[Blood platelets: neuronal model in psychiatric disorders].
L'Encephale, 1985There are some evidences to propose blood platelets as a model of bioaminergic neurons. Similarities between platelets and neurons are particularly important with respect to serotonin metabolism but now it is possible to extend this model to other neurotransmitters such as dopamine, GABA, glutamate... The reason for these similarities may be due to the
C, Dreux, J M, Launay
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Molecular Disorders of Red Blood Cells, Platelets, and Coagulation System
2017This chapter comprehensively describes not only the molecular origin of disorders of red blood cells, coagulation factors, fibrinolytic proteins, and platelets but also the clinical manifestations, diagnostic procedures, therapeutic approaches, and management of affected patients.
Mayer Jennifer L.R., Root Allen W.
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Circulating tumour DNA — looking beyond the blood
Nature Reviews Clinical Oncology, 2022Ann Tivey, Matt Church, Natalie Cook
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The blood–tumour barrier in cancer biology and therapy
Nature Reviews Clinical Oncology, 2021Patricia S Steeg
exaly
Membrane abnormalities in congenital disorders of human blood platelets.
Progress in clinical and biological research, 1983The information on membrane defects found in inherited disorders of platelet function is very limited. It has been presented here mainly in the form of a catalog of conditions in which membrane defects occur. Precise knowledge concerning the exact nature of the membrane defects is just beginning to appear in the literature.
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