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Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|January 8, 2015
Breaking bad news, the diagnosis of cystic fibrosis in childhoodTrudy Havermans, Jessica Tack, Anneke Vertommen, et al.Journal of Child Health Care : for Professionals Working with Children in the Hospital and Community|October 25, 2013
Belgian siblings of children with a chronic illness: Is their quality of life different from their peers?Trudy Havermans, Ilse De Croock, Trui Vercruysse, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|August 10, 2020
The impact of the COVID-19 pandemic on the emotional well-being and home treatment of Belgian patients with cystic fibrosis, including transplanted patients and paediatric patientsTrudy Havermans, Janne Houben, Francois Vermeulen, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 11, 2011
Guiding principles on how to manage relevant psychological aspects within a CF team: interdisciplinary approachesRita M Nobili, Alistair J A Duff, Gerald Ullrich, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|May 27, 2014
European Cystic Fibrosis Society Standards of Care: Framework for the Cystic Fibrosis CentreSteven Conway, Ian M Balfour-Lynn, Karleen De Rijcke, et al.Plos One|December 21, 2019
Assessing gastro-intestinal related quality of life in cystic fibrosis: Validation of PedsQL GI in children and their parentsMieke Boon, Ine Claes, Trudy Havermans, et al.The Lancet. Respiratory Medicine|October 2, 2019
The future of cystic fibrosis care: a global perspectiveScott C Bell, Marcus A Mall, Hector Gutierrez, et al.Pageof 2