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急性荨麻疹
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  acute urticaria
     The results showed that the number of CD3+and CD4+cells in the urticaria group was significantly lower than that of control group (P< 0.01), especially in patients with acute urticaria.
     结果表明 ,荨麻疹患者CD3+及CD4 +细胞明显降低 ,与健康对照组比较差异有非常显著性意义(P<0.01),其中以急性荨麻疹患者CD3+、CD4+改变最为明显。
短句来源
     CONCLUSION:Compound glycyrrhizin(100ml/d)was safe and effective for the treatment of acute urticaria.
     结论:复方甘草酸苷(100ml/d)是治疗急性荨麻疹安全、有效的药物。
短句来源
     Results In the acute urticaria group, the cure rate was 36%, the obvious effective rate was 60% and the total effective rate was 81%.
     结果 急性荨麻疹临床治愈率为 36 % ,显效率为 6 0 % ,总有效率为 81% ;
短句来源
     Analysis on the Drug Utilization of Oral H_1-receptor Antagonist on Treatment of Acute Urticaria in An Inland and A Coastal Hospital
     内地、沿海治疗急性荨麻疹3569例口服H_1受体拮抗剂使用分析
短句来源
     Methods Ninty-eight school children patients (age,6~12 years) with acute urticaria were divided into two groups: 49 patients received oral cetirizine once 10mg daily and the others 2/3 tablet oral ketotifen fumarate twice daily for 7d.
     方法 6 ~12岁急性荨麻疹病人 98例 ,分别给予口服西替利嗪 (4 9例 ,10mg ,1次 /d)及酮替芬 (4 9例 ,2 /3片 ,2次 /d) ,均用药 7d ;
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  “急性荨麻疹”译为未确定词的双语例句
     METHODS:72patients were randomly divided into3groups:group A were administrated with200mg/d hydrocoˉtison sodium succinate for a week; group B were administered with100ml/d compound glycyrrhizin and group C were adminˉistered with40ml/d compound glycyrrhizin for a week.
     方法:将72例急性荨麻疹患者随机均分为3组,A组给予氢化可地松琥珀酸钠注射液200mg/d,B组和C组分别给予复方甘草酸苷注射液100ml/d、40ml/d,静脉滴注,连用7d;
短句来源
     Clinical analysis of 85 cases Urticaria due to acute effective
     以感染诱发的急性荨麻疹85例临床分析
短句来源
     The effect rate 86.11% in urticaria acute;
     以皿治林治疗急性荨麻疹的有效率为86·11%;
短句来源
     The courses of therapy were 7 d in acute patients and 30 d in chronic patients.
     疗程为急性荨麻疹 7d ,慢性荨麻疹 30d。
短句来源
     Results; 70% cases of a-cute urticaria showed the response in 2 hours. 88% Itching, 86% wheals and 83% erythema were relieved after 1 hr.
     结果:急性荨麻疹患者70%在2h内起效,1h内88%患者瘙痒开始减轻,86%患者风团数开始减少,83%患者红晕程度开始减轻;
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  相似匹配句对
     ECG changes in children with acute urticaria.
     儿童急性荨麻疹的心电图观察
短句来源
     Clinical Effect of Compound Glycyrrhizin Injection in Treatment of Acute Urticaria
     复方甘草甜素治疗急性荨麻疹的临床疗效
短句来源
     Acute Appendictics
     急性阑尾炎
短句来源
     Acute Posterior Ischemic Optic Neuropathy
     急性后部缺血性视神经病变
短句来源
     Autoimmune urticaria
     自身免疫性荨麻疹
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  acute urticaria
In contrast to acute urticaria, etiology cannot be identified in most cases of chronic urticaria.
      
Acute urticaria is commonly observed in the prodromic stage of hepatitis A and B infection as well as in hepatitis C infection, although only rare cases have been published regarding the latter.
      
The absence of specific presentation of acute urticaria in, patients with viral hepatitis is not surprising because many other viral infections can induced similar cutaneous symptoms.
      
At acute urticaria and young patients with chronic urticaria there were not many secretory anomalies found out.
      
We compared the levels of neutrophil activation and related cytokines in patients with ASA-intolerant acute urticaria (AIAU) and ASA-intolerant chronic urticaria (AICU).
      
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The theraputic results of acute urticaria, papular urticaria and acute eczema with Tuo Ming He Ji made from author's ne-w prescription were Presented. It suggested, the rate of efficacy to acute urticaria was 93.62%, among which cure rate was 6.70%, effectual rate was 27.6%. The rate of efficacy to papular urticatia was 96.3%,among which cure rate was 74.07%, effectual rate was 18.54%. The rate of efficacy to acute eczema was 92.00%, among which cure rate was 56.00% The therapeutic results of this medicine to...

The theraputic results of acute urticaria, papular urticaria and acute eczema with Tuo Ming He Ji made from author's ne-w prescription were Presented. It suggested, the rate of efficacy to acute urticaria was 93.62%, among which cure rate was 6.70%, effectual rate was 27.6%. The rate of efficacy to papular urticatia was 96.3%,among which cure rate was 74.07%, effectual rate was 18.54%. The rate of efficacy to acute eczema was 92.00%, among which cure rate was 56.00% The therapeutic results of this medicine to the diseases above were not statistical significant by contrast of two groups, (P>0.05) , which suggested the therapeutic results of this medicine to various diseases above were near to one another.

报告了用自拟新方制成的“脱敏合剂”对急性荨麻疹丘疹性荨麻疹和急性湿疹治疗的情况。结果表明:该合剂对急性荨麻疹的有效率为93.62%。其中,治愈率为61.70%,显效率为27.66%。对丘疹性荨麻疹的有效率为96.30%。其中,治愈率为74.07%,显效率为18.52%。对急性湿疹的有效率为92.00%。其中,痊愈率为56.00%,该合剂对上述各病种的疗效,两两相比,均无统计学意义(P>0.05),提示该合剂对上述各病种疗效相近。

s The abnormal reaction and sero-antibody response to the concentrated (>=2.5 IU)and unconcentrated (ordinary) rabies vaccines has been observed.The abnormal reaction rate were 1.31% and 0.73% for the concentrated and unconcentrated respectively,the difference was statistically significant (X 2=6.94,P<0.01).The main clinic manifestation of the abnormal reaction,for the concentrated rabies vaccine were pain,swollen,itchy in the area of injection,and ...

s The abnormal reaction and sero-antibody response to the concentrated (>=2.5 IU)and unconcentrated (ordinary) rabies vaccines has been observed.The abnormal reaction rate were 1.31% and 0.73% for the concentrated and unconcentrated respectively,the difference was statistically significant (X 2=6.94,P<0.01).The main clinic manifestation of the abnormal reaction,for the concentrated rabies vaccine were pain,swollen,itchy in the area of injection,and the acute urticaria even allergic shock.But the serotransverse rate for the concentrated vaccine reached above 40% within 7 days,100% within 14 days after vaccination compare with those of unconcentrated only 40% within 14 days. Still nore the antibody was sufficient enough to protect suffering from the rabies within 7 days after vaccination.lt indicates that the concentrated rabies vaccine characterized by its antibody emerged quickly and high level as well.It is also discussed how to reduce the abnormal reaction for the people whom received concentrated vaccine.

报导了≥2.5IU浓缩狂苗人体接种后的不良反应其反应率为1.31%与以往未浓缩常规苗的反应率为0.73%比较两者具有显著性差异(X2=6.94,P<0.01),浓缩苗以注射1~3针时的不良反应多,临床表现以局部极痛、红肿、瘙痒、急性荨麻疹和过敏性休克等。但其血清抗体阳转率7天时为40.0%以上,14天时为100%,而常规苗仅是40.0%,抗体滴度浓缩苗第7天时达到有效保护水平(中和试验)。显示了其抗体产生早,水平高特点,关于如何减少浓缩狂苗不良反应问题,作者提出了几点建议

AIM: to observe the clinical effects of triprolidine in treating urticaria. METHODS: Patients (M 45, F 72; age 33.0±s 1.5 a) suffering from urticaria were randomly divided into 2 groups, the treatment group of 60 patients and the control group of 57 patients. The courses of disease were 2.0±1.7 a and 2.0±1.9 a respectively. The treatment group received triprolidine 5 mg, po, bid, and the control group received chlorphenamine maleate 8 mg, po, tid. The courses of therapy were 7 d in acute patients and 30 d in...

AIM: to observe the clinical effects of triprolidine in treating urticaria. METHODS: Patients (M 45, F 72; age 33.0±s 1.5 a) suffering from urticaria were randomly divided into 2 groups, the treatment group of 60 patients and the control group of 57 patients. The courses of disease were 2.0±1.7 a and 2.0±1.9 a respectively. The treatment group received triprolidine 5 mg, po, bid, and the control group received chlorphenamine maleate 8 mg, po, tid. The courses of therapy were 7 d in acute patients and 30 d in chronic patients. RESUTLS: The total effective rates of the triprolidine and chlorphenamine maleate groups were 83% and 53%, respectively (P<0.01). Triprolidine maintained a longer effective time and no serious adverse reactions were found. CONCLUSION: Triprolidine is an effective drug in treating urticaria.

目的 :观察曲普利啶对荨麻疹的疗效。方法 :117例患荨麻疹病人 ,男性 4 5例 ,女性 72例 ;年龄33.0±s 1.5a。分为治疗组 60例 ,对照组 57例。病程分别为 2 .0± 1.7a与 2 .0± 1.9a。治疗组用曲普利啶胶囊 5mg ,po ,bid ;对照组用马来酸氯苯那敏 8mg ,po ,tid。疗程为急性荨麻疹 7d ,慢性荨麻疹 30d。结果 :曲普利啶组总有效率为 83% ,与马来酸氯苯那敏组的 53%比较有显著性差异 (P<0 .0 1)。结论 :曲普利啶是治疗荨麻疹有效药物

 
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