
Często zadawane pytania
Często zadawane pytania dotyczące mukowiscydozy
Referencje
-
Orenstein DM. Cystic Fibrosis: A Guide for Patient and Family [Przewodnik dla pacjenta i rodziny]. 3. wydanie Philadelphia, PA: Lippincott Williams & Wilkins; 2004.
-
Derichs N. 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.
-
D.Sands et al Mukowiscydoza - choroba wieloukładowa, Poznań 2018
-
D.Sands et al Mukowiscydoza - choroba wieloukładowa, Poznań 2018
-
MacDonald K, McKenzie K, Zeitlin P. Cystic Fibrosis Transmembrane Regulator Protein Mutations. Pediatric Drugs2007; 9(1): 1 ̶ 10.
-
Cystic Fibrosis Trust Annual Data Report 2017; Published August 2018.
-
Annual report from Cystic Fibrosis Registry of Ireland; 2016 Annual Report.
-
Cystic Fibrosis Trust. FAQs. How common is CF? Available at: https://www.cysticfibrosis.org.uk/what-is-cystic-fibrosis/faqs#How common is cystic fibrosis? Accessed February 2019.
-
O'Sullivan B, Freedman S. Cystic fibrosis. The Lancet 2009; 373(9678): 1891 ̶ 1904.
-
The Clinical and Functional Translation of CFTR (CFTR2) resources. How is CF inherited. Available at: https://www.cftr2.org/resources. Accessed February 2019.
-
CFTR2. CFTR2 Variant List History. 8 December 2017. Available at: https://www.cftr2.org/mutations_history. Accessed February 2019.
-
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.
-
Cystic Fibrosis Trust. Nutrition: A guide for children and parents with cystic fibrosis. 2013.
-
Cystic Fibrosis Trust. Nutrition: A guide for adults with cystic fibrosis. 2010.
-
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.