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Palabras clave – provistas por la editorial

non-IgE mediated allergy; n/a; randomized controlled trials; infant; “Probiotics”[Mesh]; children; safety; therapeutic microbiology; zinc; prevention; Lactobacillus; cow’s milk protein; constipation; hepcidin; infants; Bifidobacterium; Bifidobacterium breve; allergy; asthma; functional abdominal pain disorders; probiotic strain; formula feeding; probiotic; nutritional programming; 2?-fucosyllactose; “Pregnancy”[Mesh]; colic; iron absorption; bifidobacteria; Newborn”[Mesh]; breast feeding; neonatal; diversity; acute diarrhea; celiac disease; human milk oligosaccharide; acute gastroenteritis; human milk oligosaccharides; tolerance acquisition; iron deficiency anemia; infantile colic; Lacto-N-neotetraose; gluten free diet; oligosaccharides; preterm; preterm infant; microbial programming; paediatrics; Lactobacillus reuteri; functional constipation; protein hydrolyzed formulas; oral rehydration solution; gluten-free diet; infant formula; prebiotic; Childhood Asthma Control Test; microbiome; intestinal transit time; prebiotics; sepsis; probiotics; microbiota; “Infant; lactobacilli; human milk; functional gastrointestinal disorders; inulin; fecal microbiota; Bacillus clausii; peak expiratory flow rate; breast milk; immunoglobulin E; efficacy; intestinal microbiota; necrotizing enterocolitis; pediatrics; growth