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Mortality and morbidity were monitored during suckling mice infection, immunize/challenge experiments and mixed intracranial infections.
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All study subjects were treated with oral iron for 28 days and morbidity was monitored through surveillance at health centres.
Morbidity was monitored throughout the malaria transmission season and study children were seen at the end of the malaria transmission season.
Body weight, clinical symptoms, signs of morbidity, and survival were monitored for 7 or up to 13 days.
Animals were then challenged with 10 LD50 of the highly pathogenic A/Vietnam/1203/2004 virus intranasally, and morbidity and mortality were monitored for 21 days after the viral challenge.
Body weight, morbidity and mortality were monitored for 20 28 days.
To determine whether overexpression of Mcl-1 or loss of Bak increased the risk of morbidity, cohorts of mice were monitored for 12 months.
Mice were monitored for morbidity for 7 days.
Infected BALB/c mice were monitored for morbidity, mortality and viral replication in organs as trachea, lungs, heart, kidneys, liver, brain and spleen.
This cohort was originally recruited for a perinatal mortality and morbidity survey, and the participants were monitored throughout the school years with medical examinations.
Calf morbidity from birth to weaning were monitored and recorded daily by trained study personnel including study authors (SA and JC) while blinded to the type of colostrum fed (lacteal-derived CR or pooled MC) at enrollment.
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