Marijke Proesmans

What's new in cystic fibrosis? From treating symptoms to correction of the basic defect.

Pulmonary alveolar microlithiasis: a case report and review of the literature.

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.

Thyroid Carcinoma in a Child with Activated Phosphoinositide 3-Kinase δ Syndrome: Somatic Effect of a Germline Mutation.

Neonatal factors predictive for respiratory and gastro-intestinal morbidity after esophageal atresia repair.

New therapies for acute RSV infections: where are we?

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

Systemic Inflammation and Myelofibrosis in a Patient with Takenouchi-Kosaki Syndrome due to CDC42 Tyr64Cys Mutation.

High flow nasal cannula as respiratory support in treating infant bronchiolitis: a systematic review.

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

Transcriptomic analysis of CFTR-impaired endothelial cells reveals a pro-inflammatory phenotype.

Genomics of an endemic cystic fibrosis Burkholderia multivorans strain reveals low within-patient evolution but high between-patient diversity.

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

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

Cystic fibrosis and alpha-1 antitrypsin deficiency: case report and review of literature.

Risk factors for disease severity and increased medical resource utilization in respiratory syncytial virus (+) hospitalized children: A descriptive study conducted in four Belgian hospitals.