“Il faut continuer à poser des questions” patient reported outcome measures in cystic fibrosis: An anthropological perspective
R. Coucke(Hôpital Necker-Enfants Malades), Diana Hofmann, Maxime Hautrive, Isabelle Sermet‐Gaudelus(Hôpital Necker-Enfants Malades), Elise Lammertyn, Anna Fonts, Anne Calvert, D. Hubert(Inserm), F. Chedevergne(Hôpital Necker-Enfants Malades), Emmanuelle Bardin(Centre National de la Recherche Scientifique), Véronique Bontemps(Institut de Recherche Interdisciplinaire sur les Enjeux Sociaux), H. De Keyser, T. Havermans, Veerle Bulteel, Isabelle Honoré(Inserm), A. Chansard, Clémence Martin(Délégation Paris 5), Claire Bresnihan, Maya Kirszenbaum(Hôpital Necker-Enfants Malades), Dominique Grenet(Hôpital Foch), Pierre‐Régis Burgel(Hôpital Cochin), P. De Carli(Vaincre la Mucoviscidose), Muriel Le Bourgeois(Hôpital Necker-Enfants Malades), Jutta Bend, Kate Hayes(Cystic Fibrosis Ireland), Andreas Häger
Cited by 6
Related Papers
Gain-of-function human <i>STAT1</i> mutations impair IL-17 immunity and underlie chronic mucocutaneous candidiasis
|The Journal of Experimental Medicine|2011|797
An Official American Thoracic Society/European Respiratory Society Statement: Research Questions in Chronic Obstructive Pulmonary Disease
|American Journal of Respiratory and Critical Care Medicine|2015|217
An official American Thoracic Society/European Respiratory Society statement: research questions in COPD
|European Respiratory Journal|2015|203
<i>Pseudomonas aeruginosa</i>infection in cystic fibrosis: pathophysiological mechanisms and therapeutic approaches
|Expert Review of Respiratory Medicine|2016|170
<i>Mycobacterium abscessus</i>and Children with Cystic Fibrosis
|Emerging infectious diseases|2003|159