1.
Clin Transl Sci
; 8(4): 330-3, 2015 Aug.
Artículo
en Inglés
| MEDLINE
| ID: mdl-26053284
RESUMEN
Malnutrition is one of the earliest clinical manifestations of cystic fibrosis (CF) and is associated with poorer pulmonary and cognitive outcomes and survival later in life. Infant growth can be a responsive measure for clinical research in this age group if obtained and characterized accurately. We report here the methods to standardize and implement research-quality anthropometric measurement of infants with cystic fibrosis in the Baby Observational Nutrition Study multicenter trial.