Results 181 to 190 of about 450,255 (391)
Eating Disorders in Pregnant and Breastfeeding Women: A Systematic Review [PDF]
María Martínez-Olcina +6 more
openalex +1 more source
The association of baby‐led weaning and picky eating in children aged 2–5 years
Abstract Objectives Baby‐Led Weaning (BLW) has been anecdotally linked to healthier eating habits and lower picky eating tendencies, yet empirical evidence remains limited. This study investigates the association between BLW and picky eating in children aged 2–5 years, comparing it with traditional spoon‐feeding methods. Methods A cross‐sectional study
Francesca Denise Monica G. Layug‐Dionglay +3 more
wiley +1 more source
Abstract Objectives This study aimed to investigate the eating behaviors of preschool children who had been exposed to a restricted diet due to an oral food challenge‐confirmed diagnosis of cow's milk protein allergy (CMPA) during early infancy. Methods This prospective cohort study compared the eating behaviors of Brazilian children previously ...
Anne Jardim‐Botelho +7 more
wiley +1 more source
Background Neonatal sepsis is a major cause of morbidity and mortality worldwide. The COVID-19 pandemic has influenced its epidemiology, altering pathogen distribution and antimicrobial resistance patterns, necessitating a reassessment of neonatal ...
Leyla Sahebi +4 more
doaj +1 more source
OBJECTIVE: To determine the association between congenital toxoplasmosis and preterm birth, low birthweight and small for gestational age birth. DESIGN: Multicentre prospective cohort study.
Ancelle T +18 more
core +1 more source
Trends in breastfeeding: it is not only at the breast anymore
Sheela R. Geraghty +2 more
openalex +2 more sources
BRAZIL’S PROGRESS IN PROTECTING, PROMOTING AND SUPPORTING BREASTFEEDING FROM THE PERSPECTIVE OF THE GLOBAL BREASTFEEDING COLLECTIVE [PDF]
Daiane Sousa Melo +2 more
openalex +1 more source
Expanding the genotypic spectrum of PCSK1 deficiency: A novel mutation in severe neonatal diarrhea
Abstract Among congenital diarrhea and enteropathies (CODEs), proprotein convertase subtilisin/kexin type 1 (PCSK1) deficiency is a rare monogenic disorder, associated with severe neonatal diarrhea and polyendocrinopathies. We report an 18‐day‐old male neonate, born to consanguineous parents, presenting with persistent watery diarrhea, metabolic ...
Eleonora Saraceno +7 more
wiley +1 more source

