Hemoglobin oxygen affinity in patients with cystic fibrosis.

Validation of the Italian version of the Cystic Fibrosis Quality of Life Questionnaire (CFQoL), a disease specific measure for adults and adolescents with cystic fibrosis. Koscik

Objective: To determine the prevalence of pulmonary hypertension (PH) in patients with cystic fibrosis (CF), to compare clinical characteristics, radiographic

Pneumothorax is a common complication in cystic fibrosis patients, who can present increased morbidity caused by exacerba- tion of the respiratory manifestations of cystic

Objective: To evaluate whether respiratory therapy followed by the use of inhaled albuterol modifies the pulmonary deposition of inhaled tobramycin in patients with cystic

Validation of the Italian version of the Cystic Fibrosis Quality of Life Questionnaire (CFQoL), a disease specific measure for adults and adolescents with cystic fibrosis. Koscik

In conclusion, despite the limitations inherent in a retrospective study including a small number of patients, the results of this study indicate that most patients with

The relationship between tests of lung function and three chest radiological scoring systems in patients with cystic fibrosis.. Lung function in children and

Objective: To determine the prevalence of pulmonary hypertension (PH) in patients with cystic fibrosis (CF), to compare clinical characteristics, radiographic