Cystic fibrosis (CF)‐associated liver disease (CFLD) is a hepatobiliary complication of CF.
Current diagnostic modalities rely on nonspecific assessments, whereas liver biopsy is the …

Objective To identify the incidence and outcomes of cholestasis and meconium ileus (MI) in
infants with cystic fibrosis (CF). Design Retrospective cohort study. Setting Single-centre …

Abstract Background & aims Cystic Fibrosis related liver disease (CFLD) is the 3rd largest
cause of death in Cystic Fibrosis (CF). As advances in pulmonary therapies have increased …

Gastrointestinal, pancreatic, and hepatic signs and symptoms represent the most common
presentation of early disease among patients with cystic fibrosis and may be the initial …

Abdominal symptoms are a hallmark of Cystic fibrosis (CF). Yet, their association with
morphological abnormalities of different abdominal organs is still poorly understood. Aim …

Purpose The objective of this study was to describe the clinical phenotypes of children and
adolescents with cystic fibrosis (CF); and to assess the role of pancreatic insufficiency and …

Cystic fibrosis (CF) is a multiorgan disease, and gastrointestinal (GI) manifestations can
contribute to significant morbidity and mortality for individuals with CF. Up to 85% of patients …

Introduction: Cystic fibrosis (CF) is a genetic disease that primarily affects the respiratory
system and often leads to respiratory failure and premature death. Although pulmonary …

Cystic Fibrosis is the most common lethal autosomal recessive disorder in the white
population, affecting among other organs, the lung, the pancreas and the liver. Whereas …

Cystic Fibrosis And Liver Disease - Abstract - Europe PMC Sign in | Create an account https://orcid.org
Europe PMC Menu About Tools Developers Help Contact us Helpdesk Feedback Twitter Blog …