Improving the care of patients with cystic fibrosis (CF)

por Khan, Ahsan Aftab, Nash, Edward F, Whitehouse, Joanna, Rashid, Rifat
Publicado 2017

Preferences for Prenatal Tests for Cystic Fibrosis: A Discrete Choice Experiment to Compare the Views of Adult Patients, Carriers of Cystic Fibrosis and Health Professionals

por Hill, Melissa, Suri, Ranjan, Nash, Edward F., Morris, Stephen, Chitty, Lyn S.
Publicado 2014

A prospective pilot study of home monitoring in adults with cystic fibrosis (HOME-CF): protocol for a randomised controlled trial

por Choyce, Jocelyn, Shaw, Karen L., Sitch, Alice J., Mistry, Hema, Whitehouse, Joanna L., Nash, Edward F.
Publicado 2017

Ease of use of tobramycin inhalation powder compared with nebulized tobramycin and colistimethate sodium: a crossover study in cystic fibrosis patients with pulmonary Pseudomonas a...

por Greenwood, James, Schwarz, Carsten, Sommerwerck, Urte, Nash, Edward F, Tamm, Michael, Cao, Weihua, Mastoridis, Paul, Debonnett, Laurie, Hamed, Kamal
Publicado 2017

A prospective randomised controlled mixed-methods pilot study of home monitoring in adults with cystic fibrosis

por Nash, Edward F., Choyce, Jocelyn, Carrolan, Victoria, Justice, Edwin, Shaw, Karen L., Sitch, Alice, Mistry, Hema, Whitehouse, Joanna L.
Publicado 2022

Physical Activity in Adults with Cystic Fibrosis Receiving Intravenous Antibiotics in Hospital and in the Community§

por Khiroya, Heena, Pound, Rebecca, Qureshi, Ushna, Brown, Catherine, Barrett, Joanne, Rashid, Rifat, Whitehouse, Joanna L, Turner, Alice M, Nash, Edward F
Publicado 2015

Chest wall motion analysis in healthy volunteers and adults with cystic fibrosis using a novel Kinect-based motion tracking system

por Harte, James M., Golby, Christopher K., Acosta, Johanna, Nash, Edward F., Kiraci, Ercihan, Williams, Mark A., Arvanitis, Theodoros N., Naidu, Babu
Publicado 2016

Porphyromonas pasteri and Prevotella nanceiensis in the sputum microbiota are associated with increased decline in lung function in individuals with cystic fibrosis

por Webb, Karmel, Zain, Nur Masirah M., Stewart, Iain, Fogarty, Andrew, Nash, Edward F., Whitehouse, Joanna L., Smyth, Alan R., Lilley, Andrew K., Knox, Alan, Williams, Paul, Cámara, Miguel, Bruce, Kenneth, Barr, Helen L.
Publicado 2022

Retinopathy and microalbuminuria are common microvascular complications in cystic fibrosis-related diabetes

por Kempegowda, Punith, Sunsoa, Harbinder, Chandan, Joht S., Quinn, Lauren M., Amrelia, Prashant M., Atta, Syed Noman, Amir, Sidrah, Teh, Yee Suh, Chaudhry, Sabba, de Bray, Anne, Rashid, Rifat, Whitehouse, Joanna L., Nash, Edward F., Syed, Ateeq
Publicado 2020

Pseudomonas aeruginosa quorum sensing molecules correlate with clinical status in cystic fibrosis

por Barr, Helen L., Halliday, Nigel, Cámara, Miguel, Barrett, David A., Williams, Paul, Forrester, Douglas L., Simms, Rebecca, Smyth, Alan R., Honeybourne, David, Whitehouse, Joanna L., Nash, Edward F., Dewar, Jane, Clayton, Andrew, Knox, Alan J., Fogarty, Andrew W.
Publicado 2015

The top 10 research priorities in cystic fibrosis developed by a partnership between people with CF and healthcare providers

por Rowbotham, Nicola J, Smith, Sherie, Leighton, Paul A, Rayner, Oli C, Gathercole, Katie, Elliott, Zoe C, Nash, Edward F, Daniels, Tracey, Duff, Alistair J A, Collins, Sarah, Chandran, Suja, Peaple, Ursula, Hurley, Matthew N, Brownlee, Keith, Smyth, Alan R
Publicado 2018

Diagnostic and prognostic significance of systemic alkyl quinolones for P. aeruginosa in cystic fibrosis: A longitudinal study

por Barr, Helen L., Halliday, Nigel, Barrett, David A., Williams, Paul, Forrester, Douglas L., Peckham, Daniel, Williams, Kate, Smyth, Alan R., Honeybourne, David, L. Whitehouse, Joanna, Nash, Edward F., Dewar, Jane, Clayton, Andrew, Knox, Alan J., Cámara, Miguel, Fogarty, Andrew W.
Publicado 2017