Elise Lammertyn
- Quantitative evaluation of CF airways using HRCT, µCT and histologyBy Mieke Boon, Barbara Bosch, Elise Lammertyn, Stijn Verleden, Pieter Goeminne, Bart Vanaudenaerde, Dirk Van Raemdonck, Erik Verbeken, Geert Verleden, James Hogg, Johny Verschakelen, Lieven Dupont and Kris De BoeckMieke Boon1Department of Pediatrics, Cystic Fibrosis Centre, University Hospitals Leuven, Leuven, BelgiumBarbara Bosch1Department of Pediatrics, Cystic Fibrosis Centre, University Hospitals Leuven, Leuven, BelgiumElise Lammertyn2Leuven Lung Transplant Unit, KULeuven, Leuven, BelgiumStijn Verleden2Leuven Lung Transplant Unit, KULeuven, Leuven, BelgiumPieter Goeminne2Leuven Lung Transplant Unit, KULeuven, Leuven, BelgiumBart Vanaudenaerde2Leuven Lung Transplant Unit, KULeuven, Leuven, BelgiumDirk Van Raemdonck2Leuven Lung Transplant Unit, KULeuven, Leuven, BelgiumErik Verbeken3Department of Pathology, University Hospitals Leuven, Leuven, BelgiumGeert Verleden2Leuven Lung Transplant Unit, KULeuven, Leuven, BelgiumJames Hogg4University of British Columbia James Hogg Research Centre, St. Paul's Hospital, Vancouver, BC, CanadaJohny Verschakelen5Department of Pulmonary Radiology, University Hospitals Leuven, Leuven, BelgiumLieven Dupont2Leuven Lung Transplant Unit, KULeuven, Leuven, BelgiumKris De Boeck1Department of Pediatrics, Cystic Fibrosis Centre, University Hospitals Leuven, Leuven, Belgium
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