Patrick BergerFranois LaurentEur RadiolEuropean RadiologyDournes G, Menut F, Macey J, et al. Lung morphology assessment of cystic fibrosis using MRI with ultra-short echo time at submillimeter spatial resolution. Eur Radiol 2016; 26: 3811-3820....
Assessment Of Cystic Fibrosis Carrier Status Among Those With Exercise-associated Hyponatremia In A 161-km Ultramarathon: 1950Board #145 June 2 8:00 AM - 9:30 AMAn abstract is unavailable.doi:10.1249/01.MSS.0000401350.19472.37Douglas P. Lewis...
BIOCHEMICAL ASSESSMENT OF CILIARY ACTIVITY IN THE PRESENCE OF CYSTIC FIBROSIS (CF) SERUMSince Spock, et al. (Pediat. Res. 1:173, 1967) first observed that serum from CF patients and heterozygotes induced ciliary dysrhythmia, several "CF factor" bioassays have been described. Such methods, ...
PURPOSE: To compare a computed tomographic (CT)-based scoring system with nonimaging indexes of pulmonary status in patients with cystic fibrosis. MATERIALS AND METHODS: Pulmonary CT findings were assessed in 117 patients with cystic fibrosis, with cases classified according to three groups by age; ...
Assessing Psychosocial Distress in Cystic Fibrosis: Validation of the 'Distress in Cystic Fibrosis Scale'. Psychological distressExperiences of anxiety and depression are common in adults with Cystic Fibrosis (AwCF) (e.g. Quittner in Thorax 69:1090-1097, 2014... C Finlay,S Patel,J Evans - 《...
Assessment of nutritional status in adult patients with cystic fibrosis: whole-body bioimpedance vs body mass index, skinfolds, and leg-to-leg bioimpedance Assessment of nutritional status in adult patients with cystic fibrosis: whole-body bioimpedance vs body mass index, skin- folds, and leg-to-...
Noninvasive assessments of liver fibrosis are currently used to evaluate cystic fibrosis (CF)-related liver disease. However, there is scarce data regarding their repeatability and reproducibility, especially in children with CF. The present study aimed to evaluate the repeatability and reproducibility of...
The clearance of sulphamethoxazole (SMX), a compound metabolised primarily by the N-acetyltransferase NAT1, is increased in cystic fibrosis (CF) patients. We assessed the activity and kinetic properties of NAT1 in lysates of peripheral blood mononuclear leukocytes (MNL) from CF (n = 17) and...
The measurement of lung function is the central part of the patients with cystic fibrosis assessment but we consider that exercise testing become an important tool in the continuous evaluation which is an indicative of prognosis and functional capacity and care of these patients. The 6 minute walk...
The aim of this work was to evaluate myocardial strain analysis as a tool for the early detection of left ventricular functional changes in patients with cystic fibrosis. A total of 42 consecutive patients (mean age, 24 ± 7.5 years; 52% men) diagnosed with cystic fibrosis and referred for ...