Zoekresultaten - 4 results
The effect of enteral tube feeding in cystic fibrosis: A registry based study.
original curve before the decline, but remained below the controls. Starting ETF had no effect on rate of height gain in children. The pre-index FEV1 decline (-1.52%/year (p = 0.002)) stabilized to ...
What can the CF registry tell us about rare CFTR-mutations? A Belgian study.
(0.1-2,0) (p < 0.0001)], lower sweat chloride [96 mmol/L (64-107) vs. 104 mmol/L (97-115) (p < 0.0001)], higher FEV1 %pred [77%pred (58-96) vs. 68%pred (48-86) (p = 0.017)], were less frequently ...
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 ...
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, ...