Sarah L. Ollosson

London, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 8 publications

Telemedicine and cystic fibrosis: Do we still need face-to-face clinics?

Telemedicine and cystic fibrosis: Do we still need face-to-face clinics?

Journal: Paediatric respiratory reviews

Published: February 26, 2021

Initiating home spirometry for children during the COVID-19 pandemic - A practical guide.

Initiating home spirometry for children during the COVID-19 pandemic - A practical guide.

Journal: Paediatric respiratory reviews

Published: January 26, 2021

Clinical utility of NGS diagnosis and disease stratification in a multiethnic primary ciliary dyskinesia cohort.

Clinical utility of NGS diagnosis and disease stratification in a multiethnic primary ciliary dyskinesia cohort.

Journal: Journal of medical genetics

Published: August 13, 2019

Risk factors for situs defects and congenital heart disease in primary ciliary dyskinesia.

Risk factors for situs defects and congenital heart disease in primary ciliary dyskinesia.

Journal: Thorax

Published: May 23, 2018

Primary Ciliary Dyskinesia Due to Microtubular Defects is Associated with Worse Lung Clearance Index.

Primary Ciliary Dyskinesia Due to Microtubular Defects is Associated with Worse Lung Clearance Index.

Journal: Lung

Published: September 07, 2017

Accuracy of Immunofluorescence in the Diagnosis of Primary Ciliary Dyskinesia.

Accuracy of Immunofluorescence in the Diagnosis of Primary Ciliary Dyskinesia.

Journal: American journal of respiratory and critical care medicine

Published: February 16, 2017

High prevalence of CCDC103 p.His154Pro mutation causing primary ciliary dyskinesia disrupts protein oligomerisation and is associated with normal diagnostic investigations.

High prevalence of CCDC103 p.His154Pro mutation causing primary ciliary dyskinesia disrupts protein oligomerisation and is associated with normal diagnostic investigations.

Journal: Thorax

Published: January 16, 2017

Cyanide levels found in infected cystic fibrosis sputum inhibit airway ciliary function.

Cyanide levels found in infected cystic fibrosis sputum inhibit airway ciliary function.

Journal: The European respiratory journal

Published: September 05, 2014

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Last Updated: 09/26/2026