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治疗
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  cure 1
     71 example insides, surgical operations cut off 6 examples, afferent insides get involved the treatment 15 examples, gamma knife treatment 35 examples, surgical operation excision+ the afferent inside get involved treatment 5 examples, afferent inside get involved+the gamma knife cure 9 examples, surgical operation treatment+the afferent inside get involved+the gamma knife cure 1 example.
     71例中,手术切除6例,血管内介入治疗15例,伽玛刀治疗35例,手术切除+血管内介入治疗5例,血管内介入+伽玛刀治疗9例,手术治疗+血管内介入+伽玛刀治疗1例。
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  “治疗1”译为未确定词的双语例句
     1 case died within one year without any treatment.
     未经治疗1例,1年内死亡。
短句来源
     Method:198 inpatients with schizophrenia were divided randomly into chlorpromazine group and risperidone group. HbA1C and fasting plasma glucose were tested before treatment and at 1,2,3,6,12 month after treatment, and compared with clinical routine fasting plasma glucose test.
     方法:对198例单用氯丙嗪或利培酮治疗的精神分裂症住院患者于治疗前、治疗1、2、3、6、12个月测定HbA1C及血糖浓度并与常规血糖检测指标进行比较。
短句来源
     Results:The level of HbA1C trended to increase with the time of hospitalization and associated with the level of fasting plasma glucose and the incidence of imparied glucose regulation (IGR),whose abnormality rate was 11.6% one year after treatment.
     结果:HbA1C浓度随治疗时间延长而增高,与血糖浓度变化呈显著正相关,与血葡萄糖调节受损(IGR)的发生呈平行发展,治疗1年后异常率为11.6%。
短句来源
     Hamilton depressive scale (HAMD),social disability screening schedule (SDSS),were tested before treatment and after 1,2,4 and 8 weeks.
     采用汉密尔顿抑郁量表(HAMD)、社会功能缺陷筛选量表(SDSS),在治疗前及治疗1、2、4、8周各测定1次;
短句来源
     The patients in OAC group were treated with Omeprazole(20mg) plus Amoxicilin(1000mg)and Clarithroimycin(500mg),bid,for 7 days,then Omeprazole(20mg)qd for 3 weeks.
     OAC组,奥美拉唑20 mg+阿莫西林1 g+克拉霉素500mg,2次/d,7d,治疗1周后继续以奥美拉唑20mg,每天1次,口服3周。
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  相似匹配句对
     The total courses were 24 weeks.
     d-1,治疗24w。
短句来源
     The interval of treatment is 1 year.
     治疗时间1年。
短句来源
     (390.29±53.20)mg·L~(-1)h;
     L-1.h;
短句来源
     L~-1 were perfect exterior qualification.
     L~(-1)。
短句来源
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  cure 1
The present paper concerns further investigations in our laboratory of the correlation between mechanical and dielectric behaviour during cure (1).
      


Three new 4-amino-2-alkylsulfonyl benzoic acids, namely, 4-amino-2-methylsulfonyl benzoic acid, 4-amino-2-ethylsulfonyl benzoic acid and 4-amino-2-n-propylsulfonyl benzoic acid, have been studied for in vitro in human tuberculosis, hoping that they would surpass the p-amino- salicylic acid in activity. Contrary to our expectations, however, these new compounds have been found to be far less active than the p-amino-salicylic acid itself. The 4-amino-2-n-propyl- sulfonyl benzoic acid possesses an activity in the...

Three new 4-amino-2-alkylsulfonyl benzoic acids, namely, 4-amino-2-methylsulfonyl benzoic acid, 4-amino-2-ethylsulfonyl benzoic acid and 4-amino-2-n-propylsulfonyl benzoic acid, have been studied for in vitro in human tuberculosis, hoping that they would surpass the p-amino- salicylic acid in activity. Contrary to our expectations, however, these new compounds have been found to be far less active than the p-amino-salicylic acid itself. The 4-amino-2-n-propyl- sulfonyl benzoic acid possesses an activity in the order of 10~(-3) in concentration, while the other two compounds require still higher concentrations. Besides, we have prepared five other new compounds: 4-nitro-o-tolyl-methyl sulfide, 4- nitro-2-methylsulfonyl benzoic acid, 4-nitro-o-tolyl-ethyl sulfide, 4-nitro-o-tolyl-n-propyi sulf- fide and 4-nitro-2-n-propylsulfonyl benzoic acid.

對-氨基柳酸為現在常用的一種結核病治療藥劑。我們將其中的羥基代以-SO_(2)R,希望能增強其抑制結核桿菌的性能。我們合成了4-氨基-2-甲磺醯苯甲酸,4-氨基-2-乙磺醯苯甲酸和4-氨基-2-正丙磺醯苯甲酸三種新的化合物。在試管中試驗的結果,除最後一種化合物能在千分之一濃度的溶液中具抑制結核桿菌的性能外,其餘兩種化合物抑制結核桿菌的性能則是更低。我們在製備上述三種化合物時,曾附带合成另外五種新的化合物。

A series of 8 new compounds with the dithia-dihydrostibiol structure has been compared for the therapeutic activities against schistosomiasis japonica in white mice. Each drug, thoroughly mixed with the finely powdered food, was fed to healthy mice for 14 days, and the LD_(10) and LD_(50) were evaluated. At the dosages of LD_(10) and LD_(50), each drug was fed to treat diseased mice (beginning on the 36th day after percutaneous infection on abdomen with 40 cercariae per mouse) for 14 days. After a holding period...

A series of 8 new compounds with the dithia-dihydrostibiol structure has been compared for the therapeutic activities against schistosomiasis japonica in white mice. Each drug, thoroughly mixed with the finely powdered food, was fed to healthy mice for 14 days, and the LD_(10) and LD_(50) were evaluated. At the dosages of LD_(10) and LD_(50), each drug was fed to treat diseased mice (beginning on the 36th day after percutaneous infection on abdomen with 40 cercariae per mouse) for 14 days. After a holding period of another 14 days mice were killed. Both portal system and liver were carefully scrutinized for worms. Basing on the average number of worms remained in each mouse, the therapeutic effects of out of the 8 compounds were better than that of tartar emetic administered orally.

用小白鼠试验8种二硫锑五环化合物,在同一毒性水平上比较对於日本血吸虫病的疗效。每种药物与饲料粉混匀喂饲健康小鼠14天,求出LD_(10)及LD_(50)。以这两个剂量,分别治疗病鼠(每鼠腹部皮肤感染40条尾蚴,5周後开始给药)14天,然後停药14天解剖,详细检查门静脉系统与肝内的余存虫。根据平均每鼠余存虫数,以吐酒石为标准,比较各药的疗效。结果发现Sb-1及Sb-19口服疗效较吐酒石为优。

Acute toxicity experiment consisted of one single intraperitoneal injection, while subacute toxicity experiment consisted of one injection daily for 14 days, of tartar emetic and a subsequent 3-day holding period. The mortality of mice from tartar emetic was observed after concomitant injections of 5 testing drugs (procaine-HCl, sodium phenyl acetate, sodium α α'-dimercaptoadipate, sodium mercaptosuccinate and sodium thiosulfate). The effective detoxicants were mixed up with tartar emetic and then injected intraperitoneally,...

Acute toxicity experiment consisted of one single intraperitoneal injection, while subacute toxicity experiment consisted of one injection daily for 14 days, of tartar emetic and a subsequent 3-day holding period. The mortality of mice from tartar emetic was observed after concomitant injections of 5 testing drugs (procaine-HCl, sodium phenyl acetate, sodium α α'-dimercaptoadipate, sodium mercaptosuccinate and sodium thiosulfate). The effective detoxicants were mixed up with tartar emetic and then injected intraperitoneally, once daily for 14 days, to infected mice. The mice were killed after a holding period of another 14 days. Basing on the average number of worms remained in each mouse, the effects of detoxicants on the antibilharzial activity of tartar emetic were compared. The results were as follows: (1) In mice the acute and subacute LD_(50) after intraperitoneal injection of tartar emetic were found to be 38 and 35 mg/kg/day respectively. (2) The mortality of mice from tartar emetic could be markedly reduced by simultaneous injection of procaine, sodium phenyl acetate, sodium α α'-dimercaptoadipate and sodium mercaptosuccinate, while sodium thiosulfate did not afford any protection. (3) Procaine, sodium phenyl acetate, sodium α α'-dimercaptoadipate and sodium mercaptosuccinate did not decrease the therapeutic. activity of tartar emetic, and, moreover, procaine could significantly augment its therapeutic activity against schistosomiasis japonica.

本文叙述了5种药物(盐酸普鲁卡因、苯乙酸钠、aa′-二巯基己二酸钠、巯基丁二酸钠及硫代硫酸钠)对小白鼠腹腔注射吐酒石急性(注射1次,观察3天)及亚急性(注射14天,观察3天)中毒死亡的影响;并将其中有效解毒药分别和吐酒石混合後腹腔注射小鼠14天以治疗日本血吸虫病,然後停药14天解剖,根据平均每鼠余存虫数比较各药对於吐酒石疗效的影响。结果如下: (一)小白鼠腹腔注射吐酒石急性及亚急性LD_(50)分别为38及35毫克/千克/天。 (二)普鲁卡因、苯乙酸钠、aa′-二巯基己二酸钠及巯基丁二酸钠能使小鼠腹腔注射吐酒石急性及亚急性中毒死亡率明显地减低,而硫代硫酸钠则无效。 (三)普鲁卡因、苯乙酸钠、aa′-二巯基己二酸钠及巯基丁二酸钠4种解毒药并不减低吐酒石之疗效,其中普鲁卡因尚能提高吐酒石治疗日本血吸虫病之疗效。

 
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