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Chest|November 28, 2016
Adult Patients With Bronchiectasis: A First Look at the US Bronchiectasis Research RegistryTimothy R Aksamit, Anne E O'Donnell, Alan Barker, et al.NPJ Genomic Medicine|March 28, 2018
Improving imputation in disease-relevant regions: lessons from cystic fibrosisNaim Panjwani, Bowei Xiao, Lizhen Xu, et al.Nature Genetics|January 15, 2002
Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetryHeike Olbrich, Karsten Häffner, Andreas Kispert, et al.Annals of the American Thoracic Society|January 19, 2018
The Prevalence and Significance of Staphylococcus aureus in Patients with Non-Cystic Fibrosis BronchiectasisMark L Metersky, Timothy R Aksamit, Alan Barker, et al.American Journal of Respiratory and Critical Care Medicine|January 13, 2022
Hereditary Mucin Deficiency Caused by Biallelic Loss of Function of MUC5BGregory Costain, Zhen Liu, Vito Mennella, et al.American Journal of Respiratory and Critical Care Medicine|June 4, 2015
Pulmonary Nontuberculous Mycobacterial Infection. A Multisystem, Multigenic DiseaseEva P Szymanski, Janice M Leung, Cedar J Fowler, et al.Circulation|April 14, 2012
High prevalence of respiratory ciliary dysfunction in congenital heart disease patients with heterotaxyNader Nakhleh, Richard Francis, Rachel A Giese, et al.The European Respiratory Journal|December 23, 2017
Growth and nutritional status, and their association with lung function: a study from the international Primary Ciliary Dyskinesia CohortMyrofora Goutaki, Florian S Halbeisen, Ben D Spycher, et al.Pageof 2