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Conclusion:The radical paranasal sinus surgery combined middle meatal antrostomy are efficacious and safe in the treatment of nasal polyps and chronic sinustitis.
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论 :根治性鼻窦手术中自然窦口的处理是治疗慢性鼻窦病变伴多发性鼻息肉的有效方法。 |
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Conclusion:The recombinant adenovirus containing noggin gene has been successfully constructed by ho mologous recombination in bacteria.
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论：应用细菌内同源重组法成功构建了含小鼠 noggin 基因的重组腺病毒载体。 |
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Conclusion:The treatment effect of SHT on typhoid and paratyphoid fever was better than ampicillin and CMZ,OR=0.9(9%CI=0.～0.7),NNT=(9%CI=7.8～.7).
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论:伤寒药茶治疗伤寒、副伤寒疗效优于氨苄青霉素、头孢唑钠,其收益为OR=0.9(9%CI=0.～0.7),NNT=(9%CI=7.8～.7)。 |
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Conclusion:When only ST T changes but no pathic Q wave was observed in ECG,diagnosis of patients with CAD and hypertensive heart disease must be precautious.
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论 心电图无病理性Q波 ,仅凭ST -T改变 ,对高心病患者拟诊合并冠心病应慎重。 临床无其它冠心病危险因素 ,单以不典型胸痛为表现 ,冠脉病变的可能性小 |
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ConclusionThe defecation,miction and sexual function may recover by suturing the pudendal nerve with the peripheral nerve above the spinal injury plane in paraplegia patients.
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论 :应用脊髓损伤平面以上的周围神经与阴部神经吻合来恢复截瘫患者的排便、排尿及性功能具有可行性 |
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ConclusionThe results provide an evidence that blockade of OX-0/OX-0L costimulation by OX0-Ig can inhibit the proliferation of CD~ + T cells and impair onset and severity of HSK.
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论OX0-Ig融合蛋白能够阻断OX-0/OX-0L协同刺激途径,抑制CD+T细胞增生,阻止HSK的发病,减轻HSK的严重程度。 |
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Conclusion\ GCA is likely to develop into a drug for Gauchers disease with F I mutation.
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论 GCA有可能成为F I突变型戈谢病治疗的一种新药物。 |
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Conclusion\ The recommended dosatge of Omeprazole in the treatment of peptic ulcers in children was 0 0～0 0mg·kg - ·d - (average 0 0mg·kg - ·d - ).
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论 洛赛克口服治疗小儿消化性溃疡的合适剂量为 0 . 0～ 0 . 0mg·kg-·d-(平均0 0mg·kg-·d-)。 |
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Conclusions Increasing the dose of Fu didn't improve the curious effects,but enhanced the toxicreactions of Fu in the treatment of advanced colonic cancer with CF combined with Fu.
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论 CF与Fu 联合治疗晚期肠癌时，增加Fu 用量未能提高疗效，却增加了毒性反应。 |
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Conclusions It is possible to design an sensate paraumbilical flap with the anterior branch of the 0th or th intercostal nerve.
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可设计以第 0、肋间神经前支为神经蒂的感觉脐旁皮瓣。 |
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Conclusions A novel mutation of FBN gene with Glycine to Serine change is responsible for the ectopia lentis patients in a Chinese family.
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论 FBN基因新突变G 0A (G S)是该家系单纯性晶状体异位的致病基因突变。 |
