Рекомендации ESPEN-ESPGHAN-ECFS по диетотерапии при муковисцидозе у младенцев, детей и взрослых. Коллектив авторов
Чтение книги онлайн.

Читать онлайн книгу Рекомендации ESPEN-ESPGHAN-ECFS по диетотерапии при муковисцидозе у младенцев, детей и взрослых - Коллектив авторов страница 12

СКАЧАТЬ Fat Acids 2010;83:121-9

      35

      Gaskin KJ. Nutritional care in children with cystic fibrosis: are our patients becoming better? Eur J Clin Nutr 2013;67:558-64

      36

      Corey M, McLaughlin FJ, Williams M, Levison H. A comparison of survival, growth, and pulmonary function in patients with cystic fibrosis in Boston and Toronto. J Clin Epidemiol 1988;41:583-91

      37

      Stallings VA, Stark LJ, Robinson KA, Feranchak AP, Quinton H. 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;108:832-9

      38

      Culhane S, George C, Pearo B, Spoede E. Malnutrition in cystic fibrosis: a review. Nutr Clin Pract 2013;28:676-83

      39

      Engelen MP, Com G, Deutz NEP Protein is an important but undervalued macronutrient in the nutritional care of patients with cystic fibrosis. Curr Opin Clin Nutr Metab Care 2014;17:515-20

      40

      Corey M, McLaughlin FJ, Williams M, Levison H. A comparison of survival, growth, and pulmonary function in patients with cystic fibrosis in Boston and Toronto. J Clin Epidemiol 1988;41:583-91

      41

      McCormick J, Mehta G, Olesen HV, Viviani L, Macek Jr M, Mehta A, et al. Comparative demographics of the European cystic fibrosis population: a cross-sectional database analysis. Lancet 2010;375:1007-13

      42

      Gaskin KJ. Nutritional care in children with cystic fibrosis: are our patients becoming better? Eur J Clin Nutr 2013;67:558-64

      43

      Engelen MP, Com G, Deutz NEP Protein is an important but undervalued macronutrient in the nutritional care of patients with cystic fibrosis. Curr Opin Clin Nutr Metab Care 2014;17:515-20

      44

      Maqbool A, Schall JI, Gallagher PR, Zemel BS, Strandvik B, Stallings VA. Relation between dietary fat intake type and serum fatty acid status in children with cystic fibrosis. J Pediatr Gastroenterol Nutr 2012;55:605-11

      45

      Smyth AR, Bell SC, Bojcin S, Bryon M, Duff A, Flume P, et al. European cystic fibrosis Society standards of care: best practice guidelines. J Cyst Fibres 2014;13 (Suppl. l):S23-42

      46

      Engelen MP, Com G, Deutz NEP Protein is an important but undervalued macronutrient in the nutritional care of patients with cystic fibrosis. Curr Opin Clin Nutr Metab Care 2014;17:515-20

      47

      Stephenson AL, Mannik LA, Walsh S, Brotherwood M, Robert R, Darling PB, et al. Longitudinal trends in nutritional status and the relation between lung function and BMI in cystic fibrosis: a population-based cohort study. Am J Clin Nutr 2013;97:872-7

      48

      Zolin A, McKone E, van Rens J, Fox A, Iansa P, Preftitsi A, et al. ECFSPR annual report 2010. Karup, Denmark: European Cystic Fibrosis Society; 2014

      49

      Cystic Fibrosis Foundation Patient Registry. 2011 annual data report. Bethesda, Maryland: Cystic Fibrosis Foundation; 2011

      50

      Stallings VA, Stark LJ, Robinson KA, Feranchak AP, Quinton H. 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;108:832-9

      51

      Culhane S, George C, Pearo B, Spoede E. Malnutrition in cystic fibrosis: a review. Nutr Clin Pract 2013;28:676-83

      52

      Li L, Somerset S. Digestive system dysfunction in cystic fibrosis: challenges for nutrition therapy. Dig Liver Dis 2014;46:865-74

      53

      Perano S, Rayner CK, Couper J, Martin J, Horowitz M. Cystic fibrosis related diabetes-a new perspective on the optimal management of postprandial glycemia. J Diabetes Complicat 2014;28:904-11

      54

      Debray D, Kelly D, Houwen R, Strandvik B, Colombo С Best practice guidance for the diagnosis and management of cystic fibrosis-associated liver disease. J Cyst Fibres 2011;10(Suppl. 2):S29-36

      55

      Dodge JA, Turck D. Cystic fibrosis: nutritional consequences and management. Best Pract Res Clin Gastroenterol 2006;20:531-46

      56

      Vaisman N, Pencharz PB, Corey M, Canny GJ, Hahn E. Energy expenditure of patients with cystic fibrosis. J Pediatr 1987;111:496-500

      57

      Culhane S, George C, Pearo B, Spoede E. Malnutrition in cystic fibrosis: a review. Nutr Clin Pract 2013;28:676-83

      58

      Dodge JA, Turck D. Cystic fibrosis: nutritional consequences and management. Best Pract Res Clin Gastroenterol 2006;20:531-46

      59

      Castro M, Diamanti A, Gambarara M, Bella S, Lucidi V, Papadatou B, et al. Resting energy expenditure in young patients with cystic fibrosis receiving antibiotic therapy for acute respiratory exacerbations. Clin Nutr 2002;21: 141-4

      60

      Mc Closkey M, Redmond АО, Mc Cabe C, Pyper S, Westerterp KR, Elborn SJ. Energy balance in cystic fibrosis when stable and during a respiratory exacerbation. Clin Nutr 2004;23:1405-12

      61

      Culhane S, George C, Pearo B, Spoede E. Malnutrition in cystic fibrosis: a review. Nutr Clin Pract 2013;28:676-83

      62

      Culhane S, George C, Pearo B, Spoede E. Malnutrition in cystic fibrosis: a review. Nutr Clin Pract 2013;28:676-83

      63

      Li СКАЧАТЬ