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Number of items: 6.


Allen, Lucy, Allen, Lorna, Carr, Siobhan B, Davies, Gwyneth, Downey, Damian, Egan, Marie, Forton, Julian T, Gray, Robert, Haworth, Charles, Horsley, Alexander
et al (show 3 more authors) (2023) Future therapies for cystic fibrosis. Nature communications, 14 (1). p. 693.


Southern, Kevin W ORCID: 0000-0001-6516-9083, Barben, Jürg, Goldring, Stephen, Kneen, Rachel, Southward, Suzanne, Rajeev, Yashavi, Davies, Jane C and Bush, Andrew
(2023) Raised Intracranial Pressure in Three Children with Cystic Fibrosis Receiving Elexacaftor-Tezacaftor-Ivacaftor Modulator Therapy. American journal of respiratory and critical care medicine, 208 (1). pp. 103-105.


Mahenthiralingam, Eshwar, Weiser, Rebecca, Floto, R Andres, Davies, Jane C and Fothergill, Joanne L ORCID: 0000-0002-7012-1508
(2022) Selection of Relevant Bacterial Strains for Novel Therapeutic Testing: a Guidance Document for Priority Cystic Fibrosis Lung Pathogens. Current Clinical Microbiology Reports, 9 (4). pp. 33-45.


Barben, Jurg, Castellani, Carlo, Munck, Anne, Davies, Jane C, De Winter-de Groot, Karin M, Gartner, Silvia, Kashirskaya, Nataliya, Linnane, Barry, Mayell, Sarah J, McColley, Susanna
et al (show 8 more authors) (2021) Updated guidance on the management of children with cystic fibrosis transmembrane conductance regulator-related metabolic syndrome/cystic fibrosis screen positive, inconclusive diagnosis (CRMS/CFSPID). JOURNAL OF CYSTIC FIBROSIS, 20 (5). pp. 810-819.


Bell, Scott C, Mall, Marcus A, Gutierrez, Hector, Macek, Milan, Madge, Susan, Davies, Jane C, Burgel, Pierre-Regis, Tullis, Elizabeth, Castaos, Claudio, Castellani, Carlo
et al (show 28 more authors) (2020) The future of cystic fibrosis care: a global perspective. LANCET RESPIRATORY MEDICINE, 8 (1). pp. 65-124.


Rosenfeld, Margaret, Cunningham, Steve, Harris, William T, Lapey, Allen, Regelmann, Warren E, Sawicki, Gregory S, Southern, Kevin W ORCID: 0000-0001-6516-9083, Chilvers, Mark, Higgins, Mark, Tian, Simon
et al (show 2 more authors) (2019) An open-label extension study of ivacaftor in children with CF and a <i>CFTR</i> gating mutation initiating treatment at age 2-5 years (KLIMB). JOURNAL OF CYSTIC FIBROSIS, 18 (6). pp. 838-843.

This list was generated on Sun Feb 25 01:23:53 2024 GMT.