Consensus report on nutrition for pediatric patients with cystic fibrosis.
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Vitamin K supplementation for cystic fibrosisRecombinant growth hormone therapy for cystic fibrosis in children and young adultsVitamin D supplementation for cystic fibrosisVitamin K supplementation for cystic fibrosisVitamin D supplementation for cystic fibrosisRecombinant growth hormone therapy for cystic fibrosis in children and young adultsVitamin K supplementation for cystic fibrosisVitamin K supplementation for cystic fibrosisRecombinant growth hormone therapy for cystic fibrosis in children and young adultsVitamin D supplementation for cystic fibrosisPathophysiology of cystic fibrosis and drugs used in associated digestive tract diseasesMaintenance of nutritional status in patients with cystic fibrosis: new and emerging therapiesDiabetes in cystic fibrosis: multicenter screening results based on current guidelinesCholine supplementation alters some amino acid concentrations with no change in homocysteine in children with cystic fibrosis and pancreatic insufficiency.Vitamin B(12) status in children with cystic fibrosis and pancreatic insufficiencyA multi-center controlled trial of growth hormone treatment in children with cystic fibrosis.A retrospective study of growth hormone use in adolescents with cystic fibrosis.Growth hormone improves bone mineral content in children with cystic fibrosis.Abdominal symptoms in cystic fibrosis and their relation to genotype, history, clinical and laboratory findings.CFTR depletion results in changes in fatty acid composition and promotes lipogenesis in intestinal Caco 2/15 cellsRandomized clinical trial of behavioral intervention and nutrition education to improve caloric intake and weight in children with cystic fibrosisIncorporating genetic potential when evaluating stature in children with cystic fibrosis.Genetic factors are important determinants of impaired growth after infant cardiac surgerySuboptimal vitamin K status despite supplementation in children and young adults with cystic fibrosis.Efficacy and safety of ivacaftor in patients aged 6 to 11 years with cystic fibrosis with a G551D mutation.Clinical care guidelines for cystic fibrosis-related diabetes: a position statement of the American Diabetes Association and a clinical practice guideline of the Cystic Fibrosis Foundation, endorsed by the Pediatric Endocrine SocietyAbnormal unsaturated fatty acid metabolism in cystic fibrosis: biochemical mechanisms and clinical implications.Efficacy and Safety of a New Formulation of Pancrelipase (Ultrase MT20) in the Treatment of Malabsorption in Exocrine Pancreatic Insufficiency in Cystic Fibrosis.Cystic fibrosis transmembrane conductance regulator (CFTR) allelic variants relate to shifts in faecal microbiota of cystic fibrosis patients.Growth and pulmonary outcomes during the first 2 y of life of breastfed and formula-fed infants diagnosed with cystic fibrosis through the Wisconsin Routine Newborn Screening ProgramNew stable isotope method to measure protein digestibility and response to pancreatic enzyme intake in cystic fibrosis.Phenotypic expression of the p.Leu1077Pro CFTR mutation in Sicilian cystic fibrosis patients.Supplementation with red palm oil increases β-carotene and vitamin A blood levels in patients with cystic fibrosisDiagnosing malabsorption with systemic lipid profiling: pharmacokinetics of pentadecanoic acid and triheptadecanoic acid following oral administration in healthy subjects and subjects with cystic fibrosis.Weight and energy: parents' and children's perspectives on managing cystic fibrosis diet.Vitamin A intake and elevated serum retinol levels in children and young adults with cystic fibrosis.Can nutrition counselling be more behavioural? Lessons learned from dietary management of cystic fibrosis.Comparison of WHO and CDC growth charts in predicting pulmonary outcomes in cystic fibrosisSerum linoleic acid status as a clinical indicator of essential fatty acid status in children with cystic fibrosis.Outcome measures for clinical trials assessing treatment of cystic fibrosis lung disease.
P2860
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P2860
Consensus report on nutrition for pediatric patients with cystic fibrosis.
description
2002 nî lūn-bûn
@nan
2002 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Consensus report on nutrition for pediatric patients with cystic fibrosis.
@ast
Consensus report on nutrition for pediatric patients with cystic fibrosis.
@en
Consensus report on nutrition for pediatric patients with cystic fibrosis.
@nl
type
label
Consensus report on nutrition for pediatric patients with cystic fibrosis.
@ast
Consensus report on nutrition for pediatric patients with cystic fibrosis.
@en
Consensus report on nutrition for pediatric patients with cystic fibrosis.
@nl
prefLabel
Consensus report on nutrition for pediatric patients with cystic fibrosis.
@ast
Consensus report on nutrition for pediatric patients with cystic fibrosis.
@en
Consensus report on nutrition for pediatric patients with cystic fibrosis.
@nl
P2093
P1476
Consensus report on nutrition for pediatric patients with cystic fibrosis.
@en
P2093
Drucy Borowitz
Robert D Baker
Virginia Stallings
P304
P356
10.1097/00005176-200209000-00004
P407
P577
2002-09-01T00:00:00Z