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Ultra-low-dose thoracic CT with model-based iterative reconstruction (MBIR) in cystic fibrosis patients undergoing treatment with cystic fibrosis transmembrane conductance regulators (CFTR)
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Ultra-low-dose thoracic CT with model-based iterative reconstruction (MBIR) in cystic fibrosis patients undergoing treatment with cystic fibrosis transmembrane conductance regulators (CFTR)

Moloney, F. ; Kavanagh, R.G. ; Ronan, N.J. ; Grey, T.M. ; Joyce, S. ; Ryan, D.J. ; Moore, N. ; O'Connor, O.J. ; Plant, B.J. ; Maher, M.M.

Clinical radiology, 2021-05, Vol.76 (5), p.393.e9-393.e17 [Periódico revisado por pares]

England: Elsevier Ltd

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WS14.1 Changes in population frequency of adaptive mutations in Pseudomonas aeruginosa in an ivacaftor-treated population
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WS14.1 Changes in population frequency of adaptive mutations in Pseudomonas aeruginosa in an ivacaftor-treated population

Smalley, N.E ; Ronan, N.J ; McCarthy, M ; O'Callaghan, G ; Dandekar, A.A ; Plant, B.J

Journal of cystic fibrosis, 2016-06, Vol.15, p.S22-S23 [Periódico revisado por pares]

Elsevier B.V

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3
Ivacaftor therapy in siblings with cystic fibrosis-the potential implications of Itraconazole in dosage and efficacy
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Ivacaftor therapy in siblings with cystic fibrosis-the potential implications of Itraconazole in dosage and efficacy

Harrison, M.J ; Ronan, N.J ; Khan, K.A ; O'Callaghan, G ; Murphy, D.M ; Plant, B.J

Pulmonary pharmacology & therapeutics, 2015-04, Vol.31, p.49-50 [Periódico revisado por pares]

England: Elsevier Ltd

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4
WS07.4 Effect of ivacaftor on airway bacterial community composition in CF patients with the G551D mutation
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WS07.4 Effect of ivacaftor on airway bacterial community composition in CF patients with the G551D mutation

Mooney, D ; Ronan, N.J ; Einarsson, G ; Flanagan, E.T ; Eustace, J.A ; Tunney, M.M ; Elborn, J.S ; Plant, B.J

Journal of cystic fibrosis, 2016-06, Vol.15, p.S12-S12 [Periódico revisado por pares]

Elsevier B.V

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5
157 Ivacaftor does not produce a significant change in anti-Pseudomonas aeruginosa antibodies
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157 Ivacaftor does not produce a significant change in anti-Pseudomonas aeruginosa antibodies

Collins, A ; Ronan, N.J ; McCarthy, Y ; Daly, M ; Shortt, C ; McCarthy, M ; Fleming, C ; Howlett, C ; Hickey, C ; Murphy, D.M ; Plant, B.J

Journal of cystic fibrosis, 2017-06, Vol.16, p.S106-S106 [Periódico revisado por pares]

Elsevier B.V

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6
232 Lumacaftor/Ivacaftor is associated with a significant improvement in walk test and reduction in sweat chloride in a cohort of homozygous F508del CF patients with severe disease – a single centre experience
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232 Lumacaftor/Ivacaftor is associated with a significant improvement in walk test and reduction in sweat chloride in a cohort of homozygous F508del CF patients with severe disease – a single centre experience

Ronan, N.J ; McCarthy, Y ; James, K ; Arooj, P ; Hunt, E.B ; Shortt, C ; Fleming, C ; McCarthy, M ; Howlett, C ; Hickey, C ; Flanagan, E ; Daly, M ; Eustace, J.A ; Maher, M.M ; Plant, B.J

Journal of cystic fibrosis, 2017-06, Vol.16, p.S122-S122 [Periódico revisado por pares]

Elsevier B.V

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7
128 The metabolic consequences of CFTR modulation with ivacaftor in a single adult cystic fibrosis centre cohort
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128 The metabolic consequences of CFTR modulation with ivacaftor in a single adult cystic fibrosis centre cohort

Ronan, G ; Ronan, N.J ; Shortt, C ; Fleming, C ; Cronin, K ; McCarthy, M ; Hickey, C ; Murphy, D.M ; Eustace, J.A ; O'Halloran, D.J ; Plant, B.J

Journal of cystic fibrosis, 2015-06, Vol.14, p.S90-S90 [Periódico revisado por pares]

Elsevier B.V

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217 Medical outcomes post transition of clinical care from a paediatric cystic fibrosis care model to an adult cystic fibrosis care model – an Irish perspective
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217 Medical outcomes post transition of clinical care from a paediatric cystic fibrosis care model to an adult cystic fibrosis care model – an Irish perspective

Thornton, K.P ; Ronan, N.J ; Shortt, C ; McCarthy, M ; Fleming, C ; Daly, M ; Hickey, C ; Howlett, C ; Flanagan, E.T ; Eustace, J.A ; Murphy, D.M ; Plant, B.J

Journal of cystic fibrosis, 2016-06, Vol.15, p.S106-S106 [Periódico revisado por pares]

Elsevier B.V

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9
WS04.3 A comparison of Toll-like receptor mediated innate immune response in children with cystic fibrosis and an age matched control cohort
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WS04.3 A comparison of Toll-like receptor mediated innate immune response in children with cystic fibrosis and an age matched control cohort

Ronan, N.J ; Harrison, M.J ; Wurfel, M ; Goss, C ; Shanahan, F ; O'Callaghan, G ; O'Donovan, D ; Jennings, R ; Murphy, C ; Keating, E ; Chroinin, M. Ni ; Murphy, D.M ; Mullane, D ; Eustace, J.A ; Plant, B.J

Journal of cystic fibrosis, 2016-06, Vol.15, p.S6-S7 [Periódico revisado por pares]

Elsevier B.V

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10
WS03.3 A longitudinal, multi-centre investigation into the gut microbiota of adult CF patients – the CFMATTERS perspective
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WS03.3 A longitudinal, multi-centre investigation into the gut microbiota of adult CF patients – the CFMATTERS perspective

Fouhy, F ; Ronan, N.J ; McCarthy, Y ; Arooj, P ; Daly, M ; Flanagan, E.T ; Deane, J ; O'Sullivan, O ; Murphy, K ; Fleming, C ; McCarthy, M ; Shortt, C ; Eustace, J.A ; Shanahan, F ; Rea, M.C ; Ross, R.P ; Floto, R.A ; Harrison, M.J ; Haworth, C.S ; Dupont, L ; Stanton, C ; Plant, B.J

Journal of cystic fibrosis, 2017-06, Vol.16, p.S5-S5 [Periódico revisado por pares]

Elsevier B.V

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