Results 71 to 80 of about 81,563 (218)
Orphanet Journal of Rare DiseasesBackground Prader-Willi syndrome (PWS) is a genetic disorder characterized by abnormalities in the 15q11-q13 region. Understanding the correlation between genotype and phenotype in PWS is crucial for improved genetic counseling and prognosis.
Hiago Azevedo Cintra +10 more
doaj +1 more source
Jornal de PediatriaObjective: To evaluate the growth trajectory of head circumference and neurodevelopment, and to correlate head circumference with cognitive, language, and motor outcomes during the first two years.
Maria Luciana de Siqueira Mayrink +10 more
doaj +1 more source
Jornal de Pediatria, 2014 Objectives: to analyze the changes in human milk macronutrients: fat, protein, and lactose in natural human milk (raw), frozen and thawed, after administration simulation by gavage and continuous infusion. Method: an experimental study was performed with
Andrea D. Abranches +3 more
doaj +1 more source
DemetraObjetivo: Avaliar os desfechos neonatais adversos e fatores associados entre gestantes com diabetes mellitus gestacional e de risco gestacional habitual.
Daniele Marano Rocha +3 more
doaj +1 more source