Variability of the sweat test in children with Cystic Fibrosis previously with an inconclusive diagnosis Vito Terlizzi, Daniela Dolce
Description of children who changed diagnosis from indeterminate newborn screening to cystic fibrosis
Measuring the impact of CFTR modulation on sweat chloride in cystic fibrosis: Rationale and design of the CHEC-SC Study
Extensive CFTR sequencing through NGS in Brazilian individuals with cystic fibrosis: unravelling regional discrepancies in the country
Females with Cystic Fibrosis have a larger decrease in sweat chloride in response to lumacaftor/ivacaftor compared to males
