ObjectiveTo investigate the prevalence of carbohydrate malabsorption and bacterial overgrowth in children with cystic fibrosis (CF) and abnormal stool pattern referred for breath hydrogen testing.MethodsResults from 89 tests using lactose, sucrose and lactulose in 54 children with CF were compared with 5430 tests on children with non-CF-related stool abnormalities.ResultsChildren with CF were more frequently unable to ferment lactulose to hydrogen (39% vs. 20%, PConclusionsBacterial overgrowth and carbohydrate malabsorption, particularly of sucrose, should be considered when assessing children with CF and abnormal stool patterns
With the development of new drugs that directly affect CFTR protein function, clinical trials are be...
Cystic fibrosis (CF) is a systemic genetic disease that leads to pulmonary and digestive disorders. ...
Lactose is the most important source in mammalian milk. In normal children, Lactose is hydrolyzed by...
This thesis consists of two parts. The aim of the first part is to give a clear definition of consti...
Cirrhosis (CIR) occurs in 5–7% of cystic fibrosis (CF) patients. We hypothesized that alterations in...
Summary. Intestinal malabsorption is severe and of early onset in virtually all people who have cyst...
Cystic fibrosis can affect food digestion and nutrient absorption. The underlying mutation of the cy...
Cystic fibrosis can affect food digestion and nutrient absorption. The underlying mutation of the cy...
Background: Despite treatment with pancreatic enzyme replacement therapy (PERT), patients with cysti...
D-Lactate is produced by the intestinal biota and later absorbed into circulation. Some patients wit...
BACKGROUND: Previous studies have suggested the existence of enteropathy in cystic fibrosis (CF), wh...
Objective - To evaluate the effect of currently recommended energy rich cystic fibrosis diets on fib...
The purpose of this report is to evaluate whether a new, simple, non-invasive method for chymotrypsi...
Cystic fibrosis (CF) is a systemic genetic disease that leads to pulmonary and digestive disorders. ...
BACKGROUND AND AIMS:Cirrhosis (CIR) occurs in 5-7% of cystic fibrosis (CF) patients. We hypothesized...
With the development of new drugs that directly affect CFTR protein function, clinical trials are be...
Cystic fibrosis (CF) is a systemic genetic disease that leads to pulmonary and digestive disorders. ...
Lactose is the most important source in mammalian milk. In normal children, Lactose is hydrolyzed by...
This thesis consists of two parts. The aim of the first part is to give a clear definition of consti...
Cirrhosis (CIR) occurs in 5–7% of cystic fibrosis (CF) patients. We hypothesized that alterations in...
Summary. Intestinal malabsorption is severe and of early onset in virtually all people who have cyst...
Cystic fibrosis can affect food digestion and nutrient absorption. The underlying mutation of the cy...
Cystic fibrosis can affect food digestion and nutrient absorption. The underlying mutation of the cy...
Background: Despite treatment with pancreatic enzyme replacement therapy (PERT), patients with cysti...
D-Lactate is produced by the intestinal biota and later absorbed into circulation. Some patients wit...
BACKGROUND: Previous studies have suggested the existence of enteropathy in cystic fibrosis (CF), wh...
Objective - To evaluate the effect of currently recommended energy rich cystic fibrosis diets on fib...
The purpose of this report is to evaluate whether a new, simple, non-invasive method for chymotrypsi...
Cystic fibrosis (CF) is a systemic genetic disease that leads to pulmonary and digestive disorders. ...
BACKGROUND AND AIMS:Cirrhosis (CIR) occurs in 5-7% of cystic fibrosis (CF) patients. We hypothesized...
With the development of new drugs that directly affect CFTR protein function, clinical trials are be...
Cystic fibrosis (CF) is a systemic genetic disease that leads to pulmonary and digestive disorders. ...
Lactose is the most important source in mammalian milk. In normal children, Lactose is hydrolyzed by...