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Titlebook: Blood cells in nuclear medicine, part I; Cell kinetics and bi Max R. Hardeman,Yves Najean Book 1984 Martinus Nijhoff Publishers, The Hague

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楼主: mentor
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https://doi.org/10.1007/978-94-007-2663-5 (1). This property has been proposed to determine the platelet production time (PPT) after a single intake of aspirin (2). From a theoretical point of view, this non-isotopic method can constitute an alternative to the routine isotopic techniques for platelet kinetic measurements in stationary states.
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All-Dielectric Nonlinear Meta-OpticsThe recent developments of both culture techniques, determination of differentiation antigens by monoclonal antibodies and cytochemistry has permitted to define several classes of megakaryocytic precursors in murine and human species.
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Workshop in Computational NanophotonicsIn contrast with other myeloid series, and particularly the red cell series, relatively few methods enable to quantify platelet production. So, in clinical practice, only rough (and often questionable) estimation of platelet production can be obtained.
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https://doi.org/10.1007/978-3-319-22942-3In this paper an overview of the “state of the art” of platelet kinetics 1982, will be presented.
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https://doi.org/10.1007/978-94-007-2663-5The labelling of platelets with .In-oxinate was first introduced for imaging procedures. Autologous platelets labelled with this pure γ-emitting agent could be suitable for location of vascular thrombi in humans (1,2). Moreover, .Inoxinate presents clear advantages over currently used sodium (.Cr)-chromate for platelet kinetic studies.
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Methods of Quantification of Platelet Production in Man. A Critical AnalysisIn contrast with other myeloid series, and particularly the red cell series, relatively few methods enable to quantify platelet production. So, in clinical practice, only rough (and often questionable) estimation of platelet production can be obtained.
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Simultaneous Kinetics and External Countings of Autologous 111In-oxine Labelled Platelets and HomoloThe labelling of platelets with .In-oxinate was first introduced for imaging procedures. Autologous platelets labelled with this pure γ-emitting agent could be suitable for location of vascular thrombi in humans (1,2). Moreover, .Inoxinate presents clear advantages over currently used sodium (.Cr)-chromate for platelet kinetic studies.
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Light-Emitting Electrochemical Cellsment of blood-cells. The view that disturbances in structure or functions of individual cells form the basis of disease was first put forth by Rudolph Virchow in 1858 (1). For decades thereafter our understanding of cellular involvement was limited to the data derived from fixed images of cells unde
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