Indeed, HIV infection is often associated with increased levels of platelet activators.
2
However, the molecular mechanism governing platelet aggregation is not yet fully understood.
3
Results: Eleven of 156 patients had δ-SPD based on platelet ADP content.
4
Conclusion: Hemorrheological parameters and platelet aggregation showed specific changes following carotid stenting.
5
Conclusion: Hemorheological parameters and platelet aggregation showed specific changes following carotid stenting.
1
Conclusions: Abnormal thrombocyte and hemoglobin levels at diagnosis were associated with poorer survival.
2
The thrombocyte lineage appeared the most sensitive to irradiation.
3
Our five patients were undergoing evaluation for thrombocyte when the bone marrow biopsy revealed the presence of mastocytosis.
4
The total body Cl of ultrafilterable platinum correlated well with the creatinine Cl and the thrombocyte surviving fraction.
5
We found increased thrombocyte GPX activity at the two highest dosage levels in women only, but not in men.
1
ITP is an autoimmune disease which results in low bloodplatelet counts.
2
The present investigation has studied the influence of A23187 on bloodplatelet aggregation and secretion.
3
Heparin-induced thrombocytopenia refers to the decrease in bloodplatelet count following the administration of heparin, which is an anticoagulant.
4
However, a low dose of cyclosporine A resulted in a sustained normal range of bloodplatelet count and negative proteinuria.
5
Whole bloodplatelet aggregometry and clot signature analyzer parameters did not show any sign of activation of platelets or the coagulation system.
6
Results: During treatment the leukocyte count decreased remarkably, and the patient developed lymphopenia together with a paradoxical increase in her bloodplatelet count.
7
The low peripheral bloodplatelet count is caused by premature platelet destruction by self-reacting antibodies in addition to an impairment of platelet production.
8
The discoid form of bloodplatelets is important to their function in hemostasis.
9
Bloodplatelets are notoriously difficult to preserve in vitro for long periods of time.
10
The hemophiliac, or H gene, produces male issue with a lack of bloodplatelets.
11
One of these compounds is thromboxane, which encourages bloodplatelets to aggregate into clots.
12
Photoreceptor rod cells and bloodplatelets are remarkably different, yet both illustrate a similar phenomenon.
13
Both medicines help stimulate the production of bloodplatelets.
14
Unstimulated bloodplatelets have a characteristic discoid form supported by a circumferential band of microtubules.
15
Nanomolar concentrations of cerastocytin induce aggregation of bloodplatelets.
16
Bloodplatelets and fibrinolytic activity may play an important role in the development of these complications.