There is no evidence of a primary defect in energy metabolism in subjects with cystic fibrosis
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
Reference14 articles.
1. Nutritional assessment and management in cystic fibrosis: a consensus report;Ramsey;Am J Clin Nutr,1992
2. Nutritional management of cystic fibrosis;Pencharz;Ann Rev Nutr,1993
3. The cystic fibrosis gene and resting energy expenditure;Fried;J Pediatr,1991
4. Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA;Riordan;Science,1989
5. Multi-ion pore behaviour in the CFTR chloride channel;Tabcharani;Nature,1993
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1. Growth failure in cystic fibrosis: A true need for anabolic agents?;The Journal of Pediatrics;2005-03
2. Shwachman–Kulczycki score and resting energy expenditure in cystic fibrosis;Journal of Cystic Fibrosis;2003-09
3. Question 1 Quelle influence de l'état nutritionnel sur l'évolution de la mucoviscidose? Aspect physiopathologique des troubles nutritionnels au cours de la mucoviscidose;Archives de Pédiatrie;2003-08
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