Objective: To generate and examine evidence in support of diagnosing cystic fibrosis (CF) early through newborn screening (NBS). Study design: Using a randomized controlled trial with unique unblinding/surveillance,we...
- To study fecal elastase- 1 (E1F) and chymotrypsin (ChT) in stools for the diagnosis of pancreatic insufficiency in pediatric practice. - Materials and methods. - E1F and ChT were measured in stools of 198 children d...
Background: Cystic fibrosis (CF) is considered to be rare among individuals fr om the Indian subcontinent. Furthermore, affected individuals are reported to ex perience a more severe clinical course. Aims: It was hypo...
Objective: To assess the relationship between pancreatic enzyme therapy (PET) and the clinical outcomes of growth, abdominal pain, constipation, gassiness, and number of stools in cystic fibrosis (CF).Study design: Pa...