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After injection with DC vaccines, IFN-γ production in the treatment group was significantly increased as compared with that in the control group (P>amp;lt;0.01), and IL-4 production was decreased as compared with that in the control group (P>amp;lt;0.05).
      
The clinical overall response rate was 75% in the treatment group and 56% in control group.
      
The treatment group had better results than the control group as survival period over six months was 80% and over one year 44%.
      
In the abnormal HbA1c group, 2HPG after the study was higher in the clozapine treatment group [(9.5 ± 1.8) mmol/L] than in the risperidone treatment group [(7.4 ± 1.7) mmol/L] and the chlorpromazine treatment group [(7.3 ± 1.6) mmol/L].
      
Male apoE-/- mice were randomized into 4 groups, baseline group (n=10), control group (n=14), treatment group (n=14) and prevention group (n=14).
      
The treatment group was treated with vehicle for 8 weeks, and then was treated with the agonist T0901317 for additional 6 weeks.
      
T0901317 treatment reduced the aortic atherosclerotic lesion area by 64.2% in the prevention group and 58.3% in the treatment group.
      
The hemolymph osmotic pressure and Na+ concentration in each treatment group rose remarkably at 0.125 d or 0.25 d, while the Na+-K+-ATPase activity of gill reduced gradually with increased experiment time in 3 d.
      
The results showed that there was no significant difference between the control and treatment group in body weight, respiration rate, heart rate, body temperature, and the numbers of red and white blood cells.
      
After 16 weeks, notable steatosis, and lobular inflammation were observed in model group II rat liver, while the degree of hepatic injury was attenuated in the PGZ treatment group.
      
Whereas, in PGZ treatment group, serum levels of AST and FINS showed decreasing tendency, liver indexes, serum levels of ALT, ALP, TNF-α and HOMA-IR were significantly decreased compared with model group II.
      
In order to evaluate the programme, patients entering the study were allocated alternately to a treatment group, who were offered the facilities of the experimental service, and a control group who received conventional care.
      
Those rated at high risk were all offered the same facilities in the treatment group and hence were excluded from the comparison with the controls.
      
Of the non-high risk patients, 71 remained in the treatment group and 84 in the control group.
      
The social worker and the psychologist appeared isolated from the rest of the treatment group and seemed to work independently with the parents, in contrast to the physician who did not relate to either the parent or the patient.
      
Subjects and methods 73 Bolivian non-anemic school-age children randomly assigned to the treatment group (n=37; receiving supplements containing FeSO4 during 18 weeks) or the control group (n=36; receiving a placebo during the same period).
      
Results The treatment group did not show any significant variation in hemoglobin concentration between T0 and T18 (-1.6±10.4 g/L; P=0.40) whereas the control group showed a significant decrease in hemoglobin concentration (-4.6±10.9 g/L; P=0.03).
      
In the treatment group MPG was started as above and was continued for 4 h of reperfusion followed by an intramuscular injection at the termination of the intravenous infusion.
      
In the treatment group 5 ml reviparin was injected with the Infusasleeve catheter at a proximal pressure of 80 psi.
      
those remaining non-responsive in any treatment group.
      
 

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