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1)  Glanzmann thrombasthenia
血小板无力症
1.
Novel frame-shift mutation of 540 A deletion in GPⅡb gene from a patient with Glanzmann thrombasthenia;
一种新的GPⅡb基因540A缺失移码突变引起的血小板无力症
2.
Glanzmann thrombasthenia caused by a novel Pro126His mutation in the integrin α_(Ⅱb);
一种新的整合素α_(Ⅱb)Pro126His突变导致的遗传性血小板无力症
3.
Phenotype and genotype diagnosis in five Chinese pedigrees with Glanzmann thrombasthenia
五个遗传性血小板无力症家系的表型和基因型诊断
2)  Thrombasthenia [,θrɔmbəs'θi:niə]
血小板无力症
1.
ObjectiveTo elucidate the genetic defects in patients with Glanzmann thrombasthenia (GT) and set up the experimental basis for further exploring the pathogenesis of GT.
【目的】明确血小板无力症患者的基因缺陷 ,为进一步探讨其发病机理奠定实验基础。
3)  Glanzmann's thrombasthenia
血小板无力症
1.
Objective To investigate the significance of flow cytometry in the diagnosis of Glanzmann′s Thrombasthenia (GT).
目的 探讨流式细胞术 (flowcytometry ,FCM)对诊断血小板无力症 (Glanzmann′sThrombasthenia ,GT)的意义。
4)  Thrombasthenia/genetics
血小板无力症/遗传学
5)  Thrombocytopenia [英][,θrɔmbəusaitəu'pi:niə]  [美][,θrɑmbə,saɪtə'piniə]
血小板减少症
1.
Progress in heparin-induced thrombocytopenia:pathogenesis,diagnosis and therapy;
肝素诱导的血小板减少症的病因、诊断和治疗研究进展
2.
Clinical analysis of 387 cases of pregnancy with thrombocytopenia;
妊娠合并血小板减少症387例临床分析
3.
Efficacy of rhlL-11 in management of consolidation chemotherapy-induced thrombocytopenia in acute myeloid leukemia;
rhIL-11防治急性髓细胞白血病强化治疗所致血小板减少症的作用及其机制
6)  thrombocytosis [,θrɔmbəusai'təusis]
血小板增多症
1.
Analysis of hemogram,iron staining in bone marrow and iron metabolism in 98 patients with thrombocytosis;
98例血小板增多症患者血象、骨髓铁染色及铁代谢分析
2.
Secondary thrombocytosis due to imipenem-cilastatin sodium
亚胺培南-西司他丁钠致继发性血小板增多症
补充资料:血小板衰弱症


血小板衰弱症


  即"血小板无力症"。
  
说明:补充资料仅用于学习参考,请勿用于其它任何用途。
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