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This study administers NK1R antagonist starting the same time as the magnesium-deficient diet and hence coincides with our studies wherein we also show that a preventive regime of NK1R antagonist improved pathogenesis in the context of EMCV infection.
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This study administered the multi-attribute Health Utilities Index Mark 2 (HUI2) and HUI3 instruments to assess health status and HRQoL.
This study administered MDA as pyrimethamine (100 mg) every six months for three rounds.
Experienced fieldworkers who had been engaged in past national surveys and who were trained for this study administered the study tool in the field.
The co-investigators for this study administered the questionnaire prior to the commencement of a regular scheduled period of classroom instruction.
The researcher for this study administered a self-report questionnaire to patients to assess missed dosages over the previous one month.
Only one study reported the prevalence of parasitaemia while the MDA was ongoing and this study administered MDA as chloroquine (450mg) plus pyrimethamine (45mg) every two months for 11 rounds (Najera 1973 NGA).
This study administered a validated structured psychiatric interview (CIS-R) and additional health assessments on a diverse sample residing in an urban community setting with high levels of social deprivation.
The data used in this study was collected by a self administered mail questionnaire, and reported sick leave was the only question in this study administered as an interview during the clinical examinations administered by the HUNT research centre, and registered in the HUNT data bank.
This study administered MDA using sulfalene (500 mg) plus pyrimethamine (25 mg) every 10 weeks, and noted lessening effect between seven and 11 months (RR 0.87, 95% CI 0.73 to 1.05, one study, number sampled 3154) and no difference beyond 12 months of follow-up (RR 0.96, 95% CI 0.81 to 1.14, one study, number sampled 3261, Analysis 5.3).
Observed docetaxel data from subjects in this study administered 60 and 75 mg m−2 were overlaid with historical data from subjects dosed with 35, 75 and 100 mg m−2 docetaxel (Baker et al, 2003) to ascertain if an interaction was observed affecting docetaxel concentration time profiles.
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