Diet and Exercise in Cystic Fibrosis

<p>Section A.  OVERVIEW OF NUTRITION AND DIETS IN CYSTIC FIBROSIS<br>1. Nutrition for pregnant cystic fibrosis patients<br>2. Disordered eating and body image in cystic fibrosis <br>3. Neonatal screening and nutrition/growth in cystic fibrosis: A review  <br>4. CF Nutrition: Outcomes, Treatment Guidelines and Risk Classification<br>5. Clinical, nutritional and spirometry in cystic fibrosis            <br>6. Family mealtimes and children with cystic fibrosis<br>7. Disturbed sleep behaviors and melatonin in sleep dysfunction and treatment of cystic fibrosis<br>8. Age at diagnosis and disease progression of cystic fibrosis<br>9. Lactoferrin and cystic fibrosis airway infection<br>B. VITAMIN D DEFICIENCY AND SUPPLEMENTATION IN GROWTH AND HEALTH IN CHILDREN WITH CYSTIC FIBROSIS<br>10. Vitamin D bioavailability in cystic fibrosis<br>11. Cystic fibrosis and Vitamin D<br>12. Specialty Foods for Children with Cystic Fibrosis<br>13. The Effects of Caffeine, Alcohol, and Tobacco in Cystic Fibrosis<br>14. Fat-Soluble Vitamin Deficiency in Cystic Fibrosis<br>15. Can light provide a vitamin D supplement in cystic fibrosis?<br>16. Pediatric cystic fibrosis children and fat-soluble vitamins<br>C. VITAMIN DEFICIENCY, ANTIOXIDANTS, AND SUPPLEMENTATION IN CYSTIC FIBROSIS PATIENTS<br>17. Vitamin supplements: a role in cystic fibrosis patients?<br>18. Nutrition oxidative stress and patients with cystic fibrosis<br>19. Vitamin A Supplementation Therapy for Patients with Cystic Fibrosis<br>20. The Emergence of Polyphenols in the Potentiation of Treatment Modality in Cystic Fibrosis<br>21. Chronic infection with Pseudomonas aeruginosa in an animal model of oxidative stress: Lessons for patients with Cystic Fibrosis <br>22. Vitamin K in cystic fibrosis<br>23. Vitamin K and cystic fibrosis<br>D. MANAGEMENT OF DIABETES ASSOCIATED WITH CYSTIC FIBROSIS: ROLE OF NUTRITION AND FOOD<br>24. Insulin, body mass and growth in young cystic fibrosis patients<br>25. Low glycemic index dietary interventions in cystic fibrosis <br>26. Insulin resistance in cystic fibrosis: Management<br>E.  DIGESTIVE ENZYMES, PRO-BIOTICS AND FOOD IN TREATMENT OF INTESTINAL DYSFUNCTION<br>27. Cystic fibrosis and celiac disease<br>28. Probiotic supplementation, pulmonary exacerbations in patients with cystic fibrosis<br>F. NUTRITION AND PULMONARY FUNCTION IN CYSTIC FIBROSIS PATIENTS<br>29. CYSTIC FIBROSIS RELATED DIABETES: LUNG  FUNCTION AND NUTRITIONAL STATUS<br>30. Eating Disorders and Disturbed Eating Attitudes and Behaviors Typical in CF<br>31. Buteyko: Better Breathing = Better Health<br>G.  NUTRITION AND LIVER AND OTHER ORGANS OF CYTIC FIBROSIS PATIENTS<br>32. The pancreatic duct ligated pig model for patients suffering from exocrine pancreatic insufficiency- studies on vitamin A and E status<br>H. EXERCISE AND BEHAVIOR IN MANAGEMENT OF CYSTIC FIBROSIS<br>33. Exercise testing in CF, the what and how  <br>34. Mechanism of exercise limitation in cystic fibrosis: A literature update of involved mechanisms  <br>35. Assessing Physical Activity Levels using Questionnaires and Diaries<br>36. Motivating physical activity: Skills and Strategies for Behavior Change              <br>37. Diet, food and nutrition and exercise in cystic fibrosis <br>38. Personalizing Exercise Programs for CF patients<br>I. FAT AND LIPID METABOLISM IN CYSTIC FIBROSIS <br>39. Unsaturated fatty acids in cystic fibrosis: metabolism and therapy <br>40. Essential fatty acid deficiency in cystic fibrosis: malabsorption or metabolic abnormality? <br>41. Persistent fat malabsorption in cystic fibrosis <br>42. Omega-3 Fatty Acids and Cystic Fibrosis</p>