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Platelet function in the neonate.

作者信息

Stuart M J

出版信息

Am J Pediatr Hematol Oncol. 1979 Fall;1(3):227-34. doi: 10.1097/00043426-197923000-00006.

DOI:10.1097/00043426-197923000-00006
PMID:543516
Abstract

Impairment of platelet function is well recognized in the neonate. The abnormalities include a reduction in platelet factor 3 activity and availability, a reduction in the release of nonmetabolic storage pool ADP and ATP, and platelet factor 4 following stimulation, decreased adhesiveness, and impaired aggregation with ADP, epinephrine, collagen, and thrombin. Whether the cause of the platelet abnormality and the impairment in platelet secretion is due to a "storage pool deficiency" or an "aspirin-like defect" has been unclear. However, recent data suggests that the neonatal platelet possesses neither a significant deficiency in prostaglandin synthesis nor a significant decrease in storage pool adenine nucleotides. The abnormalities noted appear most likely to be due to a membrane-related phenomenon.

摘要

相似文献

1
Platelet function in the neonate.
Am J Pediatr Hematol Oncol. 1979 Fall;1(3):227-34. doi: 10.1097/00043426-197923000-00006.
2
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3
Prostaglandins in platelet function.血小板功能中的前列腺素
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Platelet secretion defect associated with impaired liberation of arachidonic acid and normal myosin light chain phosphorylation.
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Malondialdehyde formation as an indicator of prostaglandin production by human platelets.丙二醛的形成作为人类血小板产生前列腺素的指标。
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Influence of epinephrine on the aggregation response of aspirin-treated platelets.肾上腺素对阿司匹林处理过的血小板聚集反应的影响。
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Platelet aggregation independent of ADP release or prostaglandin synthesis in patients with hermansky-Pudlak syndrome.Hermansky-Pudlak综合征患者中不依赖于ADP释放或前列腺素合成的血小板聚集
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[Aspirin-like defect - a hereditary thrombocytopathy due to impaired release of platelet adenosine diphosphate].[阿司匹林样缺陷——一种因血小板二磷酸腺苷释放受损导致的遗传性血小板病]
Bilt Hematol Transfuz. 1979;7(2-3):165-74.

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