• 2861 Citations
  • 22 h-Index
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Fingerprint Fingerprint is based on mining the text of the experts' scientific documents to create an index of weighted terms, which defines the key subjects of each individual researcher.

  • 18 Similar Profiles
Cystic Fibrosis Medicine & Life Sciences
Cystic Fibrosis Transmembrane Conductance Regulator Medicine & Life Sciences
Lung Medicine & Life Sciences
Mucus Medicine & Life Sciences
Mucociliary Clearance Medicine & Life Sciences
Lung Diseases Medicine & Life Sciences
Epithelial Sodium Channels Medicine & Life Sciences
Therapeutics Medicine & Life Sciences

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Projects 2000 2020

Research Output 1996 2018

1 Citations

Changes in lung clearance index in preschool-aged patients with cystic fibrosis treated with ivacaftor (GOAL): A clinical trial

Ratjen, F., Klingel, M., Black, P., Powers, M. R., Grasemann, H., Solomon, M., Sagel, S. D., Donaldson, S. H., Rowe, S. M. & Rosenfeld, M., Aug 15 2018, In : American Journal of Respiratory and Critical Care Medicine. 198, 4, p. 526-528 3 p.

Research output: Contribution to journalLetter

Cystic Fibrosis
Clinical Trials

Critical Care of the Adult Patient With Cystic Fibrosis

King, C. S., Brown, A. W., Aryal, S., Ahmad, K. & Donaldson, S. H., Jan 1 2018, (Accepted/In press) In : Chest.

Research output: Contribution to journalArticle

Critical Care
Cystic Fibrosis
Patient Care
Exocrine Pancreatic Insufficiency

Homogeneity of Aerosol Deposition and Mucociliary Clearance are Improved Following Ivacaftor Treatment in Cystic Fibrosis

Bennett, W. D., Zeman, K. L., Laube, B. L., Wu, J., Sharpless, G., Mogayzel, P. J. & Donaldson, S. H., Aug 1 2018, In : Journal of Aerosol Medicine and Pulmonary Drug Delivery. 31, 4, p. 204-211 8 p.

Research output: Contribution to journalArticle

Mucociliary Clearance
Cystic Fibrosis
2 Citations

Ivacaftor withdrawal syndrome in cystic fibrosis patients with the G551D mutation

Trimble, A. T. & Donaldson, S. H., Mar 1 2018, In : Journal of Cystic Fibrosis. 17, 2, p. e13-e16

Research output: Contribution to journalArticle

Cystic Fibrosis
Withholding Treatment
Clinical Trials

SPLUNC1 degradation by the cystic fibrosis mucosal environment drives airway surface liquid dehydration

Webster, M. J., Reidel, B., Tan, C. D., Ghosh, A., Alexis, N. E., Donaldson, S. H., Kesimer, M., Ribeiro, C. M. P. & Tarran, R., Oct 1 2018, In : European Respiratory Journal. 52, 4, 1800668.

Research output: Contribution to journalArticle

Cystic Fibrosis
Clone Cells