Search results - 5 results
The effect of enteral tube feeding in cystic fibrosis: A registry based study.
(CF) remains equivocal. METHODS: A Belgian CF registry based, retrospective, longitudinal study, evaluated the pre- and post- ETF (n = 113) clinical evolution and compared each patient with 2 age, ...
What can the CF registry tell us about rare CFTR-mutations? A Belgian study.
in CF-disease liability is hardly documented. METHODS: Belgian CF-Registry 2013 data were analyzed to identify CF with at least 1 RM (CF + RM). Clinical data and sweat chloride of CF + RM were compared ...
Ethnicity impacts the cystic fibrosis diagnosis: A note of caution.
analysis of the CFTR2 and UK CF databases for clinical phenotype, sweat chloride values and CFTR mutations and compared the diagnostic characteristics of Asian to non-Asian patients with CF. RESULTS: Asian ...
Treatment burden in patients with at least one class IV or V CFTR mutation
phenotype, but little is known about their relative treatment burden. We compared treatment burden between patients with two class I, II, or III mutations and patients with at least one mutation of class IV /V ...
Is there evidence for correct diagnosis in cystic fibrosis registries?
comparing similar cohorts. OBJECTIVE AND METHODS: Explore patient characteristics in Belgian (B), French (F), German (G) and Dutch (NL) registries (total N=13,122) and determine whether they fulfill ...