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LUNG, ISSN 0341-2040, 02/2020, Volume 198, Issue 1, pp. 151 - 156
Purpose Cystic fibrosis (CF) is a multisystem genetic disease caused by dysfunction of the epithelial anionic channel Cystic Fibrosis Transmembrane conductance... 
Bicarbonate | AIRWAY ION-TRANSPORT | GENE | PROTOCOLS | RESPIRATORY SYSTEM | Cystic fibrosis | Pseudomonas aeruginosa | CFTR | SEVERITY | Genetic disease
Journal Article
Journal Article
JORNAL BRASILEIRO DE PNEUMOLOGIA, ISSN 1806-3713, 05/2017, Volume 43, Issue 3, pp. 219 - 245
ABSTRACT Cystic fibrosis (CF) is an autosomal recessive genetic disorder characterized by dysfunction of the CFTR gene. It is a multisystem disease that most... 
TRANSMEMBRANE CONDUCTANCE REGULATOR | PSEUDOMONAS-AERUGINOSA INFECTION | RESPIRATORY SYSTEM | LONG-TERM AZITHROMYCIN | RECOMBINANT HUMAN DNASE | ALLERGIC BRONCHOPULMONARY ASPERGILLOSIS | HIGH-DOSE IBUPROFEN | QUALITY-OF-LIFE | PLACEBO-CONTROLLED TRIAL | RESISTANT STAPHYLOCOCCUS-AUREUS | INTESTINAL-OBSTRUCTION SYNDROME
Journal Article
NUTRICION HOSPITALARIA, ISSN 0212-1611, 11/2011, Volume 26, Issue 6, pp. 1322 - 1327
Background & aims: Malnutrition is related with pulmonary disease. The aim was to analyze the association of lung function respectively to nutritional status,... 
NUTRITION & DIETETICS | Pulmonary function | GROWTH | LUNG-FUNCTION | Cystic fibrosis | BODY-COMPOSITION | Nutritional status | CHILDREN
Journal Article
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