Analysis of exocrine pancreatic function in cystic fibrosis: one mild CFTR mutation does not exclude pancreatic insufficiency
- 1 September 2001
- journal article
- research article
- Published by Wiley in European Journal of Clinical Investigation
- Vol. 31 (9) , 796-801
- https://doi.org/10.1046/j.1365-2362.2001.00876.x
Abstract
Background Cystic fibrosis (CF) is the most common cause of exocrine pancreatic insufficiency in childhood. The aim of the present study is to evaluate the correlation between genotype and exocrine p...Keywords
This publication has 19 references indexed in Scilit:
- Comparison of Fecal Elastase-1 Determination with the Secretin-Cholecystokinin Test in Patients with Cystic FibrosisScandinavian Journal of Gastroenterology, 1999
- Clinical evaluation of the faecal elastase test in the diagnosis and staging of chronic pancreatitisEuropean Journal of Gastroenterology & Hepatology, 1996
- Genotype-phenotype relationships in a cohort of adult cystic fibrosis patientsEuropean Respiratory Journal, 1996
- Microsatellite Haplotypes of Polish Cystic Fibrosis Alleles: ΔF508 Chromosomes Demonstrate a North-South Haplotype Frequency GradientHuman Heredity, 1996
- Independent genetic determinants of pancreatic and pulmonary status in cystic fibrosisThe Lancet, 1990
- Pancreatic Function in Infants Identified as Having Cystic Fibrosis in a Neonatal Screening ProgramNew England Journal of Medicine, 1990
- Haplotypes in cystic fibrosis patients with or without pancreatic insufficiency from four European populationsGenomics, 1989
- Identification of the Cystic Fibrosis Gene: Genetic AnalysisScience, 1989
- Identification of the Cystic Fibrosis Gene: Cloning and Characterization of Complementary DNAScience, 1989
- Familial concordance of pancreatic function in cystic fibrosisThe Journal of Pediatrics, 1989