Résultats de la recherche - 4 results
What can the CF registry tell us about rare CFTR-mutations? A Belgian study.
Society) nomenclature, were listed in supplementary data. Seven transplanted CF + RM were excluded for further analysis. CF + RM had higher age at diagnosis [median (IQR)] [3.7 y (0.3-18.3) vs. 0.3y ...
Ethnicity impacts the cystic fibrosis diagnosis: A note of caution.
Cuppens, Harry; Amaral, Margarida; De Boeck, Kris Source: J Cyst Fibros, Volume 16, Issue 4, p.488-491 (2017) Abstract: BACKGROUND: The diagnosis of Cystic Fibrosis (CF) is by consensus based on the same ...
Treatment burden in patients with at least one class IV or V CFTR mutation
at time of diagnosis. Health Topics: Mucoviscidosis Mucoviscidose Mucoviscidose Service: Étude des soins de santé Gezondheidszorgonderzoek Health services research Manuscript versions: DOI: ...
Is there evidence for correct diagnosis in cystic fibrosis registries?
predefined diagnostic criteria. RESULTS: Using as case definition sweat chloride >60mmol/L or 2 CFTR mutations identified, CF diagnosis was not documented in 2.8, 5.7, 6.5 and 21.6% of subjects in the F, B, ...