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Pediatrics|June 1, 1990
Newborn screening for cystic fibrosis is complicated by age-related decline in immunoreactive trypsinogen levelsM J Rock, E H Mischler, P M Farrell, et al.The New England Journal of Medicine|February 12, 1998
Nutritional benefits of neonatal screening for cystic fibrosis. Wisconsin Cystic Fibrosis Neonatal Screening Study GroupP M Farrell, M R Kosorok, A Laxova, et al.Pediatrics|April 3, 1998
Acquisition of Pseudomonas aeruginosa in children with cystic fibrosisP M Farrell, G Shen, M Splaingard, et al.Microscopy Research and Technique|October 10, 2006
Analysis of changes in optical fibers during arc-fusion splicing by use of quantitative phase imagingN M Dragomir, E Ampen-Lassen, G W Baxter, et al.Pediatric Pulmonology|September 25, 2001
Acceleration of lung disease in children with cystic fibrosis after Pseudomonas aeruginosa acquisitionM R Kosorok, L Zeng, S E West, et al.Molecular Genetics and Metabolism|December 6, 2011
CFTR mutation analysis and haplotype associations in CF patientsS K Cordovado, M Hendrix, C N Greene, et al.Pediatrics|January 3, 2001
Early diagnosis of cystic fibrosis through neonatal screening prevents severe malnutrition and improves long-term growth. Wisconsin Cystic Fibrosis Neonatal Screening Study GroupP M Farrell, M R Kosorok, M J Rock, et al.Journal of Clinical Microbiology|August 6, 2005
Early immune response to the components of the type III system of Pseudomonas aeruginosa in children with cystic fibrosisR Corech, A Rao, A Laxova, et al.Diabetes|January 1, 1982
Complications of pregnancy and fetal developmentP M Farrell, M J Engle, I D Frantz, et al.The Journal of Pediatrics|April 17, 1998
Growth status in children with cystic fibrosis based on the National Cystic Fibrosis Patient Registry data: evaluation of various criteria used to identify malnutritionH C Lai, M R Kosorok, S A Sondel, et al.Pageof 15