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The close association between colonization and the subsequent clinical infection has also been demonstrated in infants staying in MRSA-endemic neonatal intensive care units [16].
The localized anesthetic action of tetracaine has been demonstrated in infants after 30 minutes [ 17].
Transfer of functional tuberculin-specific immune cells, as evidenced by delayed-type hypersensitivity (DTH), has been demonstrated in infants from vaccinated mothers [ 18].
The effect of probiotics on preventing AD has been demonstrated in infants of the Finnish pregnant mothers with a strong family history of eczema, allergic rhinitis, or asthma.
Whereas endogenous production of SIgA has been demonstrated in infants in developing countries, it may take several years before the concentrations of intestinal SIgA achieve adult levels in developed countries where exposure to environmental and dietary microbes is lower.
For example, antigen specific proliferative responses and cytokine production have been demonstrated in infants vaccinated against measles virus [ 28], and neonatal mice vaccinated against measles virus [ 29, 30] and lymphocytic choriomeningitis virus [ 31] following vaccination in the face of antigen-specific MDI.
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Growth, safety, and a decrease in invasive fungal infections have been demonstrated in preterm infants who received bLf (100 mg/day) [ 10].
Somato-sensory responses have been demonstrated in young infants, but these cannot yet serve as endpoints; we first need to establish normal values of voltage, frequency, and duration.
Increased non respiratory morbidity in early term infants has been demonstrated in a cohort of infants with mature fetal lung indices [ 35].
Benefits of IPT with SP have been demonstrated in pregnant women [33], infants [8], and children [11].
Reduced insulin sensitivity has been demonstrated in cord blood of infants exposed to maternal hyperglycemia (5).
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