« Previous
Next »
Journal of Cystic Fibrosis
Volume 9, Issue 2
, Pages 135-142
, March 2010
Incorporating genetic potential when evaluating stature in children with cystic fibrosis
References
- . National Cystic Fibrosis Patients Registry Annual Data Report, 2004. Bethesda, MD; 2005;
- Young adults with cystic fibrosis are shorter than healthy peers because their parents are also short. Eur J Pediatr. 2005;164:781–782
- . Classification of nutritional status in cystic fibrosis. Curr Opin Pulm Med. 2006;12:422–427
- . Standards for childrens height at ages 2–9
years allowing for height of parents. Arch Dis Child. 1970;45:755–762 - . Parent-specific height standards for preadolescent children of 3 racial groups, with methods for rapid determination. Pediatrics. 1973;52:555–560
- . Parent-specific adjustments for assessment of recumbent length and stature. Monogr Paediatr. 1981;13:
- . In: second edition. Human growth. 3:New York: Plenum Press; 1986;p. 104–107
- . Parent-specific adjustments for evaluation of recumbent length and stature of children. Pediatrics. 1985;75:304–313
- . Growth evaluation: parent and child specific height standards. Arch Dis Child. 1989;64:5
- . Consensus report on nutrition for pediatric patients with cystic fibrosis. J Pediatr Gastroenterol Nutr. 2002;35:246–259
- 2000 CDC Growth Charts for the United States: methods and development. Vital Health Stat Ser. 2002;11:1–190
- . Growth, maturation, and body composition: the Fels Longitudinal Study 1929–1991. Cambridge, United Kingdom: Cambridge university Press; 1992;
- . The changing epidemiology of cystic fibrosis. J Pediatr. 1993;122:1–9
- . Pulmonary function between 6 and 18
years of age. Pediatr Pulmonol. 1993;15:75–88 - . Statistical methods for rates and proportions. New York: John Wiley and Sons; 1981;
- . The measurement of observer agreement for categorical data. Biometrics. 1977;33:159–174
- Merrill RM, Richardson. Validity of self-reported height, weight, and body mass index: findings from the National Health and Nutrition Examination Survey, 2001–2006. Prev Chronic Dis 2009;6(4). http://www.cdc.gov/pcd/issues/2009/oct/08_0229.htm.
- . Classification of malnutrition in cystic fibrosis: implications on evaluating and benchmarking clinical practices. Am J Clin Nutr. 2008;88:161–166
- . Improving subspecialty healthcare: lessons from cystic fibrosis. J Pediatr. 2005;147:295–301
- . Improvements in healthcare: how can we change outcome?. J Pediatr. 2005;147:279–281
- . Evidence-based practice recommendations for nutrition-related management of children and adults with cystic fibrosis and pancreatic insufficiency: results of a systematic review. J Am Diet Assoc. 2008;108:832–839
- U.S. Census Bureau. Population estimates Program. Race and Hispanic origin in 2005. http://www.census.gov/population/pop-profile/dynamic/RACEHO.pdf.
- . Parent-specific adjustments for assessment of recumbent length and stature. Monogr Paediatr. 1981;13:1–81
PII: S1569-1993(10)00007-X
doi: 10.1016/j.jcf.2010.01.003
© 2010 European Cystic Fibrosis Society. Published by Elsevier Inc All rights reserved.
« Previous
Next »
Journal of Cystic Fibrosis
Volume 9, Issue 2
, Pages 135-142
, March 2010
