Kris De Boeck Department of Development and Regeneration, Woman and Child Unit, CF research lab KU Leuven Biography Publications Institution JoVE Articles Kris De Boeck has not added a biography. If you are Kris De Boeck and would like to personalize this page please email our Author Liaison for assistance. Publications Assays of CFTR Function In Vitro, Ex Vivo and In Vivo International Journal of Molecular Sciences. Jan, 2022 | Pubmed ID: 35163362 A Comparative Analysis of Pricing and Reimbursement of Cystic Fibrosis Transmembrane Conductance Regulator Modulators in Europe Frontiers in Pharmacology. 2021 | Pubmed ID: 34858177 Rectal Organoid Morphology Analysis (ROMA) As a Promising Diagnostic Tool in Cystic Fibrosis Thorax. 11, 2021 | Pubmed ID: 33859053 Correction of CFTR Function in Intestinal Organoids to Guide Treatment of Cystic Fibrosis The European Respiratory Journal. 01, 2021 | Pubmed ID: 32747394 Author Correction: Allele Specific Repair of Splicing Mutations in Cystic Fibrosis Through AsCas12a Genome Editing Nature Communications. Oct, 2020 | Pubmed ID: 33093446 Cystic Fibrosis Drug Trial Design in the Era of CFTR Modulators Associated with Substantial Clinical Benefit: Stakeholders' Consensus View Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. 09, 2020 | Pubmed ID: 32527602 Phenotyping of Rare Mutations Reveals Distinct Trafficking and Functional Defects Cells. 03, 2020 | Pubmed ID: 32204475 Defining Polysaccharide Antibody Deficiency: Measurement of Anti-Pneumococcal Antibodies and Anti-Salmonella Typhi Antibodies in a Cohort of Patients with Recurrent Infections Journal of Clinical Immunology. 01, 2020 | Pubmed ID: 31705452 Changing Epidemiology of the Respiratory Bacteriology of Patients with Cystic Fibrosis-data from the European Cystic Fibrosis Society Patient Registry Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. 05, 2020 | Pubmed ID: 31492646 Lung Function Evolution in Children with Old and New Type Bronchopulmonary Dysplasia: a Retrospective Cohort Analysis European Journal of Pediatrics. Dec, 2019 | Pubmed ID: 31486896 Allele Specific Repair of Splicing Mutations in Cystic Fibrosis Through AsCas12a Genome Editing Nature Communications. 08, 2019 | Pubmed ID: 31391465 No Easy Road to Better Cystic Fibrosis Care in Eastern Europe? Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. 07, 2018 | Pubmed ID: 29859834 Where Are We with Transformational Therapies for Patients with Cystic Fibrosis? Current Opinion in Pharmacology. 06, 2017 | Pubmed ID: 28992608 The Diagnosis of Cystic Fibrosis Presse Medicale (Paris, France : 1983). Jun, 2017 | Pubmed ID: 28576637 Fifth Percentile Cutoff Values for Antipneumococcal Polysaccharide and Anti- Vi IgG Describe a Normal Polysaccharide Response Frontiers in Immunology. 2017 | Pubmed ID: 28553290 Ethnicity Impacts the Cystic Fibrosis Diagnosis: A Note of Caution Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. Jul, 2017 | Pubmed ID: 28233695 Does Newborn Screening Influence the Young Cystic Fibrosis Cohort Included in National Registries? The European Respiratory Journal. 01, 2017 | Pubmed ID: 28077474 New Horizons for Cystic Fibrosis Treatment Pharmacology & Therapeutics. 02, 2017 | Pubmed ID: 27916649 Equitable CF Care As a Basic Human Right Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. 11, 2016 | Pubmed ID: 27751793 A Novel Translational Model for Fetoscopic Intratracheal Delivery of Nanoparticles in Piglets Prenatal Diagnosis. Oct, 2016 | Pubmed ID: 27567969 Classification of CFTR Mutation Classes - Authors' Reply The Lancet. Respiratory Medicine. 08, 2016 | Pubmed ID: 27377413 Progress in Therapies for Cystic Fibrosis The Lancet. Respiratory Medicine. 08, 2016 | Pubmed ID: 27053340 Disease-specific Clinical Trials Networks: the Example of Cystic Fibrosis European Journal of Pediatrics. Jun, 2016 | Pubmed ID: 26979528 The Influence of Nebulized Drugs on Nasal Ciliary Activity Journal of Aerosol Medicine and Pulmonary Drug Delivery. 08, 2016 | Pubmed ID: 26741301 Searching for a Cure for Cystic Fibrosis. A 25-year Quest in a Nutshell European Journal of Pediatrics. Jan, 2016 | Pubmed ID: 26567541 Morphometric Analysis of Explant Lungs in Cystic Fibrosis American Journal of Respiratory and Critical Care Medicine. Mar, 2016 | Pubmed ID: 26551917 RAAV-CFTRΔR Rescues the Cystic Fibrosis Phenotype in Human Intestinal Organoids and Cystic Fibrosis Mice American Journal of Respiratory and Critical Care Medicine. Feb, 2016 | Pubmed ID: 26509335 Is the Raised Volume Rapid Thoracic Compression Technique Ready for Use in Clinical Trials in Infants with Cystic Fibrosis? Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. Jan, 2016 | Pubmed ID: 25890589 Proximity to Blue Spaces and Risk of Infection with Pseudomonas Aeruginosa in Cystic Fibrosis: A Case-control Analysis Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. Nov, 2015 | Pubmed ID: 25940953 Efficacy and Safety of Ivacaftor in Patients with Cystic Fibrosis and a Non-G551D Gating Mutation Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. Dec, 2014 | Pubmed ID: 25266159 Medical Consensus, Guidelines, and Position Papers: a Policy for the ECFS Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. Sep, 2014 | Pubmed ID: 25053447 The Relative Frequency of CFTR Mutation Classes in European Patients with Cystic Fibrosis Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. Jul, 2014 | Pubmed ID: 24440181 Lung Clearance Index: Evidence for Use in Clinical Trials in Cystic Fibrosis Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. Mar, 2014 | Pubmed ID: 24315208 A New Clinical Trials Directive to Boost Academic Trials? The Lancet. Respiratory Medicine. Apr, 2013 | Pubmed ID: 24429080 Impact of Air Pollution on Cystic Fibrosis Pulmonary Exacerbations: a Case-crossover Analysis Chest. Apr, 2013 | Pubmed ID: 23081770 CFTR Biomarkers: Time for Promotion to Surrogate End-point The European Respiratory Journal. Jan, 2013 | Pubmed ID: 22878883 Guideline on the Design and Conduct of Cystic Fibrosis Clinical Trials: the European Cystic Fibrosis Society-Clinical Trials Network (ECFS-CTN) Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. Jun, 2011 | Pubmed ID: 21658644 Rectal Organoid Morphology Analysis (ROMA): A Diagnostic Assay in Cystic Fibrosis Senne Cuyx1,2, Anabela S. Ramalho1, Nikky Corthout3,4, Steffen Fieuws5, Eva Fürstová6, Kaline Arnauts7,8, Marc Ferrante7,9, Catherine Verfaillie8, Sebastian Munck3,4, Mieke Boon1,2, Marijke Proesmans1,2, Lieven Dupont10,11, Kris De Boeck1,2, François Vermeulen1,2 1Department of Development and Regeneration, Woman and Child Unit, CF research lab, KU Leuven, 2Department of Pediatrics, Pediatric Pulmonology, University Hospitals Leuven, 3VIB Bio Imaging Core, VIB-KU Leuven Center for Brain & Disease Research, 4Department for Neuroscience, KU Leuven, 5Interuniversity Center for Biostatistics and Statistical Bioinformatics, University of Leuven and University of Hasselt, 6Department of Pediatrics, 2nd Faculty of Medicine, Charles University and Motol University Hospital, 7Department of Chronic Diseases and Metabolism (CHROMETA), Translational Research Center for Gastrointestinal Disorders (TARGID), KU Leuven, 8Department of Development and Regeneration, Stem Cell Institute Leuven (SCIL), KU Leuven, 9Department of Gastroenterology and Hepatology, University Hospitals Leuven, KU Leuven, 10Department of Chronic Diseases, Metabolism and Ageing; Pneumology, KU Leuven, 11Department of Respiratory Diseases, University Hospitals Leuven JoVE 63818 Médecine
Rectal Organoid Morphology Analysis (ROMA): A Diagnostic Assay in Cystic Fibrosis Senne Cuyx1,2, Anabela S. Ramalho1, Nikky Corthout3,4, Steffen Fieuws5, Eva Fürstová6, Kaline Arnauts7,8, Marc Ferrante7,9, Catherine Verfaillie8, Sebastian Munck3,4, Mieke Boon1,2, Marijke Proesmans1,2, Lieven Dupont10,11, Kris De Boeck1,2, François Vermeulen1,2 1Department of Development and Regeneration, Woman and Child Unit, CF research lab, KU Leuven, 2Department of Pediatrics, Pediatric Pulmonology, University Hospitals Leuven, 3VIB Bio Imaging Core, VIB-KU Leuven Center for Brain & Disease Research, 4Department for Neuroscience, KU Leuven, 5Interuniversity Center for Biostatistics and Statistical Bioinformatics, University of Leuven and University of Hasselt, 6Department of Pediatrics, 2nd Faculty of Medicine, Charles University and Motol University Hospital, 7Department of Chronic Diseases and Metabolism (CHROMETA), Translational Research Center for Gastrointestinal Disorders (TARGID), KU Leuven, 8Department of Development and Regeneration, Stem Cell Institute Leuven (SCIL), KU Leuven, 9Department of Gastroenterology and Hepatology, University Hospitals Leuven, KU Leuven, 10Department of Chronic Diseases, Metabolism and Ageing; Pneumology, KU Leuven, 11Department of Respiratory Diseases, University Hospitals Leuven JoVE 63818 Médecine