ePS2.10 Exercise testing and training in cystic fibrosis clinics in the United Kingdom: a 10-year update by Tomlinson, O.W, Williams, C.A, Saynor, Z.L, Stevens, D, Urquhart, D.S

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WS01.02 The current state of play regarding exercise testing in cystic fibrosis: co-development with the community by Saynor, Z.L, Gruet, M, McNarry, M.A, Button, B, Morrison, L, Wagner, M, Sawyer, A, Hebestreit, H, Stanford, G.E, Radtke, T, Urquhart, D.S

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EPS1.03 Feasibility of obtaining submaximal outcomes in people with advanced cystic fibrosis lung disease undergoing cardiopulmonary exercise testing by Urquhart, D.S, Burns, P, Jamieson, P, Barry, P.J, Waller, I, Petch, N, Sovtic, A, Gojsina, B, Verges, S, de Maat, T, Morrison, L, Wood, J, Crute, S, Williams, C.A, Tomlinson, O.W, Quon, B.S, Kwong, E, Saynor, Z.L, Causer, A.J, Dwyer, T, Stevens, D, Remus, N, Douvry, B, Foster, K, Hebestreit, H, Radtke, T

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WS01.01 Cardiopulmonary exercise testing provides prognostic information in advanced cystic fibrosis lung disease by Radtke, T, Urquhart, D.S, Braun, J, Barry, P, Waller, I, Petch, N, Mei-Zahav, M, Kramer, M.R, Hua-Huy, T, Dinh-Xuan, A.T, Innes, J.A, McArthur, S, Sovtic, A, Gojsina, B, Verges, S, de Maat, T, Morrison, L, Wood, J, Crute, S, Williams, C.A, Tomlinson, O.W, Bar-Yoseph, R, Hebestreit, A, Quon, B.S, Kwong, E, Saynor, Z.L, Causer, A.J, Stephenson, A.L, Schneiderman, J.E, Shaw, M, Dwyer, T, Stevens, D, Remus, N, Douvry, B, Foster, K, Ratjen, F, Benden, C, Hebestreit, H

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The impact of plasma 25-hydroxyvitamin d on lung function in patients with cystic fibrosis by Causer, A.J, Saynor, Z.L, Arregui-Fresneda, I, Connett, G, Allenby, M.I, Daniels, T, Carroll, M.P, Urquhart, D.S, Revuelta Iniesta, R

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WS16.2 The reliability of maximal cardiopulmonary exercise testing for young cystic fibrosis patients by Williams, C.A, Saynor, Z.L, Barker, A.R, Oades, P.J

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168 A protocol to determine O2max in young patients with cystic fibrosis: recommendations for clinical practice by Saynor, Z.L, Barker, A.R, Oades, P.J, Williams, C.A

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Exercise testing in cystic fibrosis: Who and why? by Urquhart, D.S., Saynor, Z.L.

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WS08.1 The utility of oxygen uptake efficiency as a marker of aerobic fitness in children with cystic fibrosis by Tomlinson, O.W., Barker, A.R., Chubbock, L.V., Stevens, D., Saynor, Z.L., Oades, P.J., Williams, C.A.

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WS08.3 Combined ramp and supramaximal cardiopulmonary exercise testing for individuals with cystic fibrosis by Saynor, Z.L., Causer, A.J., Allenby, M.I., Carroll, M., Connett, G., Daniels, T., Shute, J.K., Cummings, M.H., Shepherd, A.I.

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