中华医学杂志
2015年 · 第95卷第18期
中华医学杂志
应重视真性红细胞增多症的基础和临床研究
polycythemia vera (PV) is a clonal and chronic myeloproliferative tumor mainly caused by abnormal proliferation of red blood cells leading to increased red blood cell volume. Determining that JAK2 and MPL are the initiating mutant genes that cause PV will be negative throughout the Philadelphia chromosome (Ph–) The study of myeloproliferative tumors has brought into the era of molecular targeting.
真性红细胞增多症70例临床特点及疗效分析
老年真性红细胞增多症患者临床特征及预后分析
BCR-ABL阴性MPN患者CALR、JAK2及MPL基因突变分析
单中心真性红细胞增多症816例生存现状及预后分析
无创性预测乙肝肝硬化门脉高压性胃病的Logistic回归模型
中性粒细胞/淋巴细胞计数比值在老年人肺部细菌感染诊断中的临床应用
遗传性凝血因子Ⅶ缺乏症患者致病基因分析
三尖瓣成形术与置换术治疗合并右心衰竭的中重度三尖瓣关闭不全的效果分析
不同治疗策略在慢性肾疾病合并无保护左主干病变中的应用
院内获得性念珠菌血症的临床特征及其影响因素
青藏高原藏族高原红细胞增多症与EDNRA基因遗传多态性的关系
SDF–1/CXCR4轴在MSCs移植促进SD大鼠急性心肌梗死心脏功能恢复中的作用
基质金属蛋白酶9在Wistar大鼠与自发性高血压大鼠烟熏肺损伤中的变化
术前与术中内镜下括约肌切开术治疗胆囊结石合并胆总管结石的荟萃分析
成人全身多发重症静脉血管畸形综合征的治疗探讨
As a new type of vascular diseases in the world, venous vascular malformations have become the most frequent and common lesions in congenital vascular malformations. In the past, it was often called cavernous hemangioma. Its pathological characteristics and clinical manifestations are essentially different from hemangioma. Its lifelong progressive development is the main source of health hazard of this disease. Severe venous vascular malformation syndrome is a large area severe venous vascular malformation combined with multiple organ involvement and accompanied by significant coagulation dysfunction syndrome, which is relatively rare in the world. At present, in view of the lack of understanding of severe venous vascular malformation syndrome in the world and the lack of uniform name, the author temporarily uses this name to explain and discuss the rare cases of systemic multiple severe venous malformation syndrome in clinic.
过敏性哮喘特异性免疫治疗中调节性T细胞与辅助性T细胞的动态变化
Allergic asthma is an allergic disease with abnormal immune function, and the incidence rate is 5% ~16%[
严重脓毒症及脓毒性休克患者抗菌药物PK/PD特点和优化治疗
Sepsis refers to a systemic inflammatory response syndrome caused by infection, with clinically confirmed presence of bacteria or highly suspected foci of infection; Severe sepsis refers to sepsis accompanied by organ dysfunction and/or signs of hypoperfusion and hypotension; Septic shock refers to severe sepsis that is still accompanied by uncorrectable persistent hypotension after sufficient fluid resuscitation, and even may be accompanied by multiple organ (more than one) dysfunction. The incidence and mortality of severe sepsis and septic shock remain high. About 1.5 million patients in North America and Europe each year, with mortality rates ranging from 35% to 50%[
BCR/ABL阴性骨髓增殖性肿瘤血管新生的研究现状
BCR/ABL fusion gene-negative myeloproliferative neoplasm (MPN) is a group of malignant myeloproliferative diseases originating from pluripotent hematopoietic stem cells, including polycythemia vera (PV), essential thrombocythemia (ET) and primary myelofibrosis (PMF). 90% of PV, half of ET and PMF patients have mutations in JAK2 V617F gene[
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