שאלות נפוצות

רפרנס

1. Orenstein DM. Cystic Fibrosis: A Guide for Patient and Family. 3rd ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2004.

   האם   חולי CF יכולים לבצע פעילות גופנית?

2. Derichs N. Targeting a genetic defect: cystic fibrosis transmembrane conductance regulator modulators in cystic fibrosis. European Respiratory Review 2013; 22(127): 58 ̶ 65.

3. Wang W, Linsdell P. Conformational change opening the CFTR chloride channel pore coupled to ATP-dependent gating. Biochimica et Biophysica Acta (BBA) - Biomembranes. 2012; 1818(3):851-860.

4. MacDonald K, McKenzie K, Zeitlin P. Cystic Fibrosis Transmembrane Regulator Protein Mutations. Pediatric Drugs. 2007; 9(1):1-10.

5. NHS Choices. Cystic Fibrosis - Diagnosis. Available from: http://www.nhs.uk/conditions/cystic-fibrosis/pages/diagnosis.aspx. Updated May 2014. Accessed June 2016.

6. Cystic Fibrosis Foundation. Testing for Cystic Fibrosis. http://www.cff.org/AboutCF/Testing/. Accessed June 2016.

7. World Health Organization. The molecular genetic epidemiology of cystic fibrosis: report of a joint meeting of WHO/ECFTN/ICF(M)A/ECFS; June 19, 2002; Genoa, Italy. World Health Organization; 2004. Available from: http://www.who.int/genomics/publications/en/HGN_WB_04.02_TOC.pdf. Accessed June 2016.

8. Farrell P. The prevalence of cystic fibrosis in the European Union. Journal of Cystic Fibrosis 7 2008: 450 ̶ 453.

9. O'Sullivan B and Freedman S. Cystic fibrosis. The Lancet. 2009; 373(9678):1891-1904.

10. US CF Foundation, Johns Hopkins University, The Hospital for Sick Children. The Clinical and Functional Translation of CFTR (CFTR2). Available from: http://www.cftr2.org/mutations_history.php. Accessed June 2016.

11. Welsh MJ, Ramsey BW, Accurso F, Cutting GR. Cystic fibrosis: membrane transport disorders. In: Valle D, Beaudet A, Vogelstein B, et al. eds. The Online Metabolic & Molecular Bases of Inherited Disease. The McGraw-Hill Companies Inc; 2004: part 21, chap 201. www.ommbid.com.

12. Borowitz D, et al. Consensus Report on Nutrition for Paediatric Patients With Cystic Fibrosis. J Pediatr Gastroenterol Nutr 2002; 35(3): 246 ̶ 59.

13. Smyth A, et al. European Cystic Fibrosis Society Standards of Care: Best Practice guidelines. J Cyst Fibros 2014; 13: S23 ̶ S42.