Mieke Boon

Hemoptysis after orthopedic surgery in an adolescent boy.

Primary ciliary dyskinesia, an orphan disease.

Primary ciliary dyskinesia: critical evaluation of clinical symptoms and diagnosis in patients with normal and abnormal ultrastructure.

Primary ciliary dyskinesia and humoral immunodeficiency--is there a missing link?

Morphometric Analysis of Explant Lungs in Cystic Fibrosis.

The Influence of Nebulized Drugs on Nasal Ciliary Activity.

Fifth Percentile Cutoff Values for Antipneumococcal Polysaccharide and Anti- Vi IgG Describe a Normal Polysaccharide Response.

Differential antiviral activities of respiratory syncytial virus (RSV) inhibitors in human airway epithelium.

Defining Polysaccharide Antibody Deficiency: Measurement of Anti-Pneumococcal Antibodies and Anti-Salmonella typhi Antibodies in a Cohort of Patients with Recurrent Infections.

Use of a mobile application for self-management of pancreatic enzyme replacement therapy is associated with improved gastro-intestinal related quality of life in children with Cystic Fibrosis.

Correction of CFTR function in intestinal organoids to guide treatment of cystic fibrosis.

Citrullination as a novel posttranslational modification of matrix metalloproteinases.

Rectal organoid morphology analysis (ROMA) as a promising diagnostic tool in cystic fibrosis.

Assays of CFTR Function In Vitro, Ex Vivo and In Vivo.

Microbial Community Composition in Explanted Cystic Fibrosis and Control Donor Lungs.