Search results - 4 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.
Publication Type: Peer reviewed scientific article Authors: De Wachter, E; Muriel Thomas; Simeon Wanyama; Seneca, S; Malfroot, A Source: Orphanet J Rare Dis, Volume 12, Issue 1, p.142 (2017) Abstract: BACKGROUND: CFTR2 provides clinical and functional inf ...
Ethnicity impacts the cystic fibrosis diagnosis: A note of caution.
parameters in all patients, yet the influence of ethnicity has only scarcely been studied. We aimed at elucidating the impact of Asian descent on the diagnosis of CF. METHODS: We performed a retrospective ...
Treatment burden in patients with at least one class IV or V CFTR mutation
Pulmonol, Volume 50, Issue 12, p.1230-6 (2015) Keywords: ADOLESCENT Ambulatory Care Facilities Anti-Bacterial Agents Child Child, Preschool Cohort Studies Cystic Fibrosis Cystic Fibrosis Transmembrane ...