血小板

The splenectomy also removes a suppressant of bone marrow platelet production or release.

脾切除术还消除了抑制骨髓生产或释放血小板的作用。

Results］In 108 patients (93.1%) routinely took antiplatelet drug orally;75 patients (64.7%) common took ACEI orally; 82 patients (70.7%) usually took beta-blocker orally; only 39 patients (33.6%) insisted on taking lipid-lowering drug orally;26 symptomless patients long-term took orally nitrate;24 symptomless patients long-term took Calcium antagonists.

结果］ 108例（93.1％）患者常规口服抗血小板药物，存在主要问题是部分患者用量偏低；75例（64.7％）患者服用ACEI；82例（70.7％）患者常规口服β-受体阻滞剂，心率达标率为39％；只有39例（33.6％）患者坚持服用调脂药；26例患者无症状长期口服硝酸酯类药物；24例患者长期口服钙通道阻滞剂。

"Further research is warranted to assess the benefit of specific interventions against stroke in elderly patients with epilepsy," Dr. Tallis says."We believe that these findings are an important contribution to current stroke-prevention strategies."

不过，她强调，进行预防治疗，如降低胆固醇药、抗高血压药、或抗血小板药是否对每个病患都合适，主要是要看他们中风与其他血管疾病的绝对风险，而不是其他特殊的风险因子。

He maximum amplitude of TEG measuresthe maximum clot strength, which is dependent on both fibrinogen leveland platelet function.

EG参数最大振幅反映正在形成的血凝块的最大强度或硬度及血凝块形成的稳定性，主要受纤维蛋白原和血小板两要素的影响。

Gene diagnosis and functional study were conducted in different pedigrees of inherited hemorrhagic and thrombotic diseases including 21 of rare coagulation factor deficiencies, 2 of Glanzmann thrombasthenia, 2 of hereditary hemorrhagic telangiectasis, 13 of AT deficiency, 16 of PC deficiency, 3 of PS deficiency and 2 of combined PC/PS deficiency.

遗传性出血病方面，对21个少见的遗传性凝血因子缺陷症家系、2个血小板无力症家系、2个出血性毛细血管扩张症家系进行了相关基因与功能的研究。遗传性血栓病方面，对13个AT缺陷家系、16个PC缺陷家系、3个PS缺陷家系和2个PC/PS联合缺陷家系进行了相关基因诊断与功能的研究。

Generally speaking, most causes the blood disease which the skin hemorrhage, the menstruation increase, through inspections and so on routine blood test, marrow may be clear about the diagnosis basically, but to minority difficult case, then must through the special examination method, like the chromosome inspection, the gene order analysis, the blood platelet accumulation function determination be able to diagnose (my branch to apply the above method to diagnose rare May-Hegglin successively recently exceptionally with heredity telangiectasis sickness pedigree each example).

一般而言，多数导致皮肤出血、月经增多的血液疾病，通过血常规、骨髓等检查可基本明确诊断，但对少数疑难病例，则需通过特殊的检测方法，如染色体检查、基因序列分析、血小板聚集功能测定才能确诊（最近我科应用上述方法先后诊断了罕见的May－Hegglin异常和遗传性毛细血管扩张症家系各一例）。

To investigate thrombocyte and erythrocyte CD35、CD44 and CD62P expression discrepancy and its biological significance of tumor metastasis.

研究血小板以及红细胞CD35、CD44和CD62P分子的表达变化与肿瘤转移的生物学意义。

The samples of thrombocyte and lymphocyte were inspected with FCM.

用流式细胞仪对制备好的血小板和淋巴细胞膜样本进行测定。

At 24 hours after transplantation, the presence of donor cells were analyzed by flow cytometry. Blood was obtained from the mouse caudal vein after transplantation to analyze the changes in number of leukocytes, erythrocytes and thrombocyte in peripheral blood.

移植后24 h，应用流式细胞仪分析骨髓中供体细胞的含量，或在移植后定期从小鼠的尾静脉取血，分析外周血中白细胞、红细胞及血小板的数量变化。

Using flow cytometry to measure expression of CD35、CD44 and CD62P on thrombocyte and erythrocyte of blood donors and patients with malignant tumors.

通过流式细胞仪测定正常人和恶性肿瘤患者血小板和红细胞CD35、CD44和CD62P的表达情况。

However, as the name（read－only memory）implies, CD disks cannot be written onorchanged in any way.

然而，正如其名字所指出的那样，CD盘不能写，也不能用任何方式改变其内容。

Galvanizes steel pallet is mainly export which suits standard packing of European Union, the North America. galvanizes steel pallet is suitable to heavy rack. Pallet surface can design plate type, corrugated and the gap form, satisfies the different requirements.

镀锌钢托盘多用于出口，替代木托盘，免薰蒸，符合欧盟、北美各国对出口货物包装材料的法令要求；喷涂钢托盘适用于重载上货架之用，托盘表面根据需要制作成平板状、波纹状及间隔形式，满足不同的使用要求。