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Publications by Kris De Boeck
Classification of CFTR Mutation Classes – Authors' Reply
Lancet Respiratory Medicine,The
Pulmonary
Respiratory Medicine
Long-Term Inhaled Dry Powder Mannitol in Cystic Fibrosis
American Journal of Respiratory and Critical Care Medicine
Pulmonary
Critical Care
Respiratory Medicine
Intensive Care Medicine
Trying to Find a Cure for Cystic Fibrosis: CFTR Biomarkers as Outcomes
European Respiratory Journal
Medicine
Pulmonary
Respiratory Medicine
Antisense Oligonucleotide Eluforsen Is Safe and Improves Respiratory Symptoms in F508DEL Cystic Fibrosis
Journal of Cystic Fibrosis
Child Health
Pulmonary
Pediatrics
Perinatology
Respiratory Medicine
Communication of Information About Reproductive and Sexual Health in Cystic Fibrosis. Patients, Parents and Caregivers' Experience
Journal of Cystic Fibrosis
Child Health
Pulmonary
Pediatrics
Perinatology
Respiratory Medicine
CFTR Activity Is Enhanced by the Novel Corrector GLPG2222, Given With and Without Ivacaftor in Two Randomized Trials
Journal of Cystic Fibrosis
Child Health
Pulmonary
Pediatrics
Perinatology
Respiratory Medicine
Lung Transplantation in Cystic Fibrosis Normalizes Essential Fatty Acid Profiles
Journal of Cystic Fibrosis
Child Health
Pulmonary
Pediatrics
Perinatology
Respiratory Medicine
Primary Ciliary Dyskinesia and Humoral Immunodeficiency - What Is the Missing Link?
Clinical and Translational Allergy
Immunology
Pulmonary
Allergy
Respiratory Medicine
Optimisation of Children Z-Score Calculation Based on New Statistical Techniques
PLoS ONE
Multidisciplinary
Disease-Specific Clinical Trials Networks: The Example of Cystic Fibrosis
European Journal of Pediatrics
Child Health
Pediatrics
Perinatology