S. Dell

Going beyond the chest X‐ray: Investigating laterality defects in primary ciliary dyskinesia

M. Knowles, M. Zariwala, M. Leigh, 2022, Pediatric pulmonology.

Founder Mutation in RSPH4A Identified in Patients of Hispanic Descent with Primary Ciliary Dyskinesia

F. Collins, M. Hazucha, J. Carson, 2013, Human mutation.

Hereditary Mucin Deficiency Caused by Biallelic Loss-of-Function of MUC5B.

C. Marshall, D. Manson, S. Walker, 2022, American journal of respiratory and critical care medicine.

Effect of Race and Ethnicity on Pulmonary Function Testing Interpretation: A CHEST/AARC/ATS/CTS Evidence Review and Research Statement.

S. Stanojevic, C. Bime, M. McCormack, 2023, Chest.

Treatment response to pulmonary exacerbation in primary ciliary dyskinesia

V. Waters, F. Ratjen, M. Solomon, 2023, Pediatric pulmonology.

First reports of primary ciliary dyskinesia caused by a shared DNAH11 allele in Canadian Inuit

R. Hegele, A. Lehman, D. Dyment, 2023, Pediatric pulmonology.

Airway Inflammation in Children with Primary Ciliary Dyskinesia.

M. Rosenfeld, H. Tiddens, T. Ferkol, 2022, Annals of the American Thoracic Society.

Olfaction and Gustation in Children With Primary Ciliary Dyskinesia

B. Papsin, F. Zawawi, E. Propst, 2023, OTO open.