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Early Life Growth Trajectories in Cystic Fibrosis are Associated with Pulmonary Function at Age 6 Years.
Sanders, Don B; Fink, Aliza; Mayer-Hamblett, Nicole; Schechter, Michael S; Sawicki, Gregory S; Rosenfeld, Margaret; Flume, Patrick A; Morgan, Wayne J.
Affiliation
  • Sanders DB; Department of Pediatrics, University of Wisconsin School of Medicine and Public Health, Madison, WI. Electronic address: dbsanders@pediatrics.wisc.edu.
  • Fink A; Cystic Fibrosis Foundation, Bethesda, MD.
  • Mayer-Hamblett N; Department of Biostatistics, University of Washington, Seattle, WA; Department of Pediatrics, University of Washington, Seattle, WA.
  • Schechter MS; Department of Pediatrics, Virginia Commonwealth University, Richmond, VA.
  • Sawicki GS; Department of Pediatrics, Boston Children's Hospital, Boston, MA.
  • Rosenfeld M; Department of Pediatrics, University of Washington, Seattle, WA.
  • Flume PA; Departments of Medicine and Pediatrics, Medical University of South Carolina, Charleston, SC.
  • Morgan WJ; Department of Pediatrics, University of Arizona, Tucson, AZ.
J Pediatr ; 167(5): 1081-8.e1, 2015 Nov.
Article in En | MEDLINE | ID: mdl-26340874

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Body Height / Body Weight / Forced Expiratory Volume / Nutritional Status / Cystic Fibrosis / Lung Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: J Pediatr Year: 2015 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Body Height / Body Weight / Forced Expiratory Volume / Nutritional Status / Cystic Fibrosis / Lung Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: J Pediatr Year: 2015 Type: Article