
Veelgestelde vragen
Veelgestelde vragen over Cystic Fibrosis
Referenties
-
Orenstein DM. Cystic Fibrosis: A Guide for Patient and Family. 3rd ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2004.
-
Derichs N et al. Targeting a genetic defect: cystic fibrosis transmembrane conductance regulator modulators in cystic fibrosis. European Respiratory Review. 2013; 22(127):58-65.
-
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.
-
MacDonald K, McKenzie K, Zeitlin P. Cystic Fibrosis Transmembrane Regulator Protein Mutations. Pediatric Drugs. 2007; 9(1):1-10.
-
NHS Choices. Cystic Fibrosis - Diagnosis. Beschikbaar op: http://www.nhs.uk/conditions/cystic-fibrosis/pages/diagnosis.aspx. Updated Mei 2014. Geraadpleegd Juni 2016.
-
Cystic Fibrosis Foundation. Testing for Cystic Fibrosis. http://www.cff.org/AboutCF/Testing/. Geraadpleegd Juni 2016.
-
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. Beschikbaar op: http://www.who.int/genomics/publications/en/HGN_WB_04.02_TOC.pdf. Geraadpleegd June 2016.
-
Farrell P. The prevalence of cystic fibrosis in the European Union. Journal of Cystic Fibrosis 7 2008: 450 ̶ 453.
-
O’Sullivan B, Freedman S. Cystic fibrosis. The Lancet 2009; 373(9678): 1891 ̶ 1904.
-
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/files/CFTR2_13August2015.pdf. Geraadpleegd Juni 2016.
-
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.
-
Borowitz D, et al. Consensus Report on Nutrition for Paediatric Patients With Cystic Fibrosis. J Pediatr Gastroenterol Nutr 2002; 35(3): 246 ̶ 259.
-
Smyth A, et al. European Cystic Fibrosis Society Standards of Care: Best Practice guidelines. J Cyst Fibros. 2014;13:S23–S42.
-
Nederlandse CF Registratie 2017. Beschikbaar op: www.ncfs.nl. Geraadpleegd oktober 2017.