Littlewood JM, MacDonald A. Rationale of modern dietary recommendations in cystic fibrosis. JR Soc Med 1987;80(Suppl 15):16-24Littlewood, J.M. & MacDonald, A. (1987) Rationale of modern dietary recommendations in cystic fibrosis. J. R. Soc. Med. 80(suppl. 15), 16-23....
Cystic fibrosis (CF) is an autosomal recessive disorder that is common in individuals of European descent. It is caused by mutations in the CFTR gene, which encodes the CF transmembrane conductance...
Because of the importance of adequate nutrition for growth in children and weight maintenance in adults, nutritional recommendations for CF take precedence over typical diabetic dietary recommendations in this patient population. View chapter Related terms: Epithelial Cells Cystic Fibrosis Transmembrane ...
Cystic Fibrosis (CF) - Learn about the causes, symptoms, diagnosis & treatment from the MSD Manuals - Medical Consumer Version.
When the blood sugar is high, it’s vital to consult with a diabetes specialist regarding dietary recommendations and any other treatment (such as anti-diabetic medications). Complications of Cystic Fibrosis A Word From Verywell Although eating the cystic fibrosis diet every day can present a chal...
Cystic Fibrosis (CF) - Learn about the causes, symptoms, diagnosis & treatment from the Merck Manuals - Medical Consumer Version.
Cystic fibrosis (CF) is the commonest recessively inherited condition in the population of the UK. It affects in 1 in 2500 live-born infants in this country (Dodge et al. 1988), approximately 85% of patients have pancreatic deficiency leading to signific
for healthy children and adults (D–A–CH dietary recommendations), US and German CF recommendations, and serum retinol concentrations from National Health and Nutrition Examination Survey (NHANES) data. Results Total vitamin A intake from food and supplementation was 315% ± 182% of D–A–CH re...
Recommendations for the management of cystic fibrosis 来自 ResearchGate 喜欢 0 阅读量: 14 作者: M Vidailhet 摘要: Excretion of haptocorrin (R binder), cobalamin, and other corrinoids was studied in meconium from cystic fibrosis (n = 4), premature (n = 3), and control neonates (n =...
Luigi Maiuri*,1,2, Valeria Raia3 and Guido Kroemer*,4,5,6,7,8,9 Etiological therapies aim at repairing the underlying cause of cystic fibrosis (CF), which is the functional defect of the cystic fibrosis transmembrane conductance regulator (CFTR) protein owing to mutations in the CFTR gene....