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American Journal of Respiratory Cell and Molecular Biology|April 27, 2010
Quantification of periciliary fluid height in human airway biopsies is feasible, but not suitable as a biomarkerUta Griesenbach, Samia Soussi, Mia B Larsen, et al.
Chest|November 29, 2012
High rhinovirus burden in lower airways of children with cystic fibrosisElisabeth Kieninger, Florian Singer, Caroline Tapparel, et al.
Thorax|September 15, 2022
Reduced lung function and health-related quality of life after treatment for pulmonary tuberculosis in Gambian children: a cross-sectional comparative studyEsin Nkereuwem, Schadrac Agbla, Azeezat Sallahdeen, et al.
American Journal of Respiratory Cell and Molecular Biology|February 2, 2008
Nasal abnormalities in cystic fibrosis mice independent of infection and inflammationTom N Hilliard, Jie Zhu, Ray Farley, et al.
Pediatric Pulmonology|April 23, 2014
Mannose-binding lectin 2 gene polymorphism and lung damage in primary ciliary dyskinesiaMassimo Pifferi, Andrew Bush, Angela Michelucci, et al.
American Journal of Respiratory and Critical Care Medicine|January 26, 2008
Increased airway smooth muscle mass in children with asthma, cystic fibrosis, and non-cystic fibrosis bronchiectasisNicolas Regamey, Matthias Ochs, Tom N Hilliard, et al.
Diagnostics (Basel, Switzerland)|December 23, 2022
Genetics in Idiopathic Pulmonary Fibrosis: A Clinical PerspectiveSpyros A Papiris, Caroline Kannengiesser, Raphael Borie, et al.
Pediatric Pulmonology|January 3, 2024
The genetic framework of primary ciliary dyskinesia assessed by soft computing analysisMassimo Pifferi, Attilio L Boner, Angela Cangiotti, et al.
Thorax|March 2, 2018
Olfactory dysfunction is worse in primary ciliary dyskinesia compared with other causes of chronic sinusitis in childrenMassimo Pifferi, Andrew Bush, Michele Rizzo, et al.
Thorax|July 3, 2015
European protocols for the diagnosis and initial treatment of interstitial lung disease in childrenAndrew Bush, Steve Cunningham, Jacques de Blic, et al.
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