Search results - 4 results
The effect of enteral tube feeding in cystic fibrosis: A registry based study.
gender, pancreatic status and genotype class-matched controls. RESULTS: At baseline ETF had a worse BMI z-score (p < 0.0001) and FEV1 % (p < 0.0001) compared to controls. Patients eventually receiving ...
What can the CF registry tell us about rare CFTR-mutations? A Belgian study.
RESULTS: Seventy-seven CF + RM were identified (77/1183 = 6.5%). Sixty-four different RM were detected, of which 21 had not been previously reported. All RM s, corresponding to HGVS (Human Genome Variation ...
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 ...
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, ...