Is Body Mass Index Associated with Better Lung Function in Children with Pancreatic-Sufficient Cystic Fibrosis?
An in-depth study of the CFTR gene enables selection of CFTR therapies for almost all individuals with CF
Cystic fibrosis patients and health care professionals’ evaluation of a remote follow up solution with digital questionnaires and phone consultations developed due to the COVID19 pandemic.
Arm muscle area as an early indicator of worsening nutritional status in children - a single centre experience
How effective are exercise interventions at increasing physical activity in people with Cystic Fibrosis?
Features of Salt Imbalance and Pseudo Barter Syndrome in hospitalized Children and Young Adults with Cystic Fibrosis.
