Literature DB >> 25714572

Use of WHO growth curves for patients with cystic fibrosis may provide a false sense of security.

Jacob Robson1, Elizabeth H Yen.   

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Year:  2015        PMID： 25714572      PMCID： PMC4348003          DOI： 10.1097/MPG.0000000000000603

Source DB:  PubMed          Journal:  J Pediatr Gastroenterol Nutr        ISSN： 0277-2116            Impact factor:   2.839


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  11 in total

1.  Comparison of the WHO child growth standards and the CDC 2000 growth charts.

Authors:  Mercedes de Onis; Cutberto Garza; Adelheid W Onyango; Elaine Borghi
Journal:  J Nutr       Date:  2007-01       Impact factor: 4.798

2.  Early diagnosis of cystic fibrosis through neonatal screening prevents severe malnutrition and improves long-term growth. Wisconsin Cystic Fibrosis Neonatal Screening Study Group.

Authors:  P M Farrell; M R Kosorok; M J Rock; A Laxova; L Zeng; H C Lai; G Hoffman; R H Laessig; M L Splaingard
Journal:  Pediatrics       Date:  2001-01       Impact factor: 7.124

3.  A CFTR potentiator in patients with cystic fibrosis and the G551D mutation.

Authors:  Bonnie W Ramsey; Jane Davies; N Gerard McElvaney; Elizabeth Tullis; Scott C Bell; Pavel Dřevínek; Matthias Griese; Edward F McKone; Claire E Wainwright; Michael W Konstan; Richard Moss; Felix Ratjen; Isabelle Sermet-Gaudelus; Steven M Rowe; Qunming Dong; Sally Rodriguez; Karl Yen; Claudia Ordoñez; J Stuart Elborn
Journal:  N Engl J Med       Date:  2011-11-03       Impact factor: 91.245

4.  Comparison of WHO and CDC growth charts in predicting pulmonary outcomes in cystic fibrosis.

Authors:  Evans Machogu; Yumei Cao; Tami Miller; Pippa Simpson; Hara Levy; Diana Quintero; Praveen S Goday
Journal:  J Pediatr Gastroenterol Nutr       Date:  2015-03       Impact factor: 2.839

5.  Growth and long-term lung function in cystic fibrosis: a longitudinal study of patients diagnosed by neonatal screening.

Authors:  Baroukh Maurice Assael; Giovanni Casazza; Patrizia Iansa; Sonia Volpi; Silvano Milani
Journal:  Pediatr Pulmonol       Date:  2009-03

6.  Growth and nutritional indexes in early life predict pulmonary function in cystic fibrosis.

Authors:  Michael W Konstan; Steven M Butler; Mary Ellen B Wohl; Marcia Stoddard; Robert Matousek; Jeffrey S Wagener; Charles A Johnson; Wayne J Morgan
Journal:  J Pediatr       Date:  2003-06       Impact factor: 4.406

7.  Better nutritional status in early childhood is associated with improved clinical outcomes and survival in patients with cystic fibrosis.

Authors:  Elizabeth H Yen; Hebe Quinton; Drucy Borowitz
Journal:  J Pediatr       Date:  2012-10-11       Impact factor: 4.406

8.  Improvements in lung function outcomes in children with cystic fibrosis are associated with better nutrition, fewer chronic pseudomonas aeruginosa infections, and dornase alfa use.

Authors:  Gary L McPhail; James D Acton; Matthew C Fenchel; Raouf S Amin; Michael Seid
Journal:  J Pediatr       Date:  2008-08-29       Impact factor: 4.406

9.  Longitudinal changes in growth parameters are correlated with changes in pulmonary function in children with cystic fibrosis.

Authors:  Michelle L Peterson; David R Jacobs; Carlos E Milla
Journal:  Pediatrics       Date:  2003-09       Impact factor: 7.124

Review 10.  Evidence-based practice recommendations for nutrition-related management of children and adults with cystic fibrosis and pancreatic insufficiency: results of a systematic review.

Authors:  Virginia A Stallings; Lori J Stark; Karen A Robinson; Andrew P Feranchak; Hebe Quinton
Journal:  J Am Diet Assoc       Date:  2008-05
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