ECFS standards of care on CFTR-related disorders: Updated diagnostic criteria von Castellani, C, De Boeck, K, De Wachter, E, Sermet-Gaudelus, I, Simmonds, NJ, Southern, KW

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ECFS standards of care on CFTR-related disorders: Towards a comprehensive program for affected individuals von De Wachter, E, De Boeck, K, Sermet-Gaudelus, I, Simmonds, NJ, Munck, A, Naehrlich, L, Barben, J, Boyd, C, Veen, SJ, Carr, SB, Fajac, I, Farrell, PM, Girodon, E, Gonska, T, Grody, WW, Jain, M, Jung, A, Kerem, E, Raraigh, KS, van Koningsbruggen-Rietschel, S, Waller, MD, Southern, KW, Castellani, C

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Letter to the editor: Risk of false newborn screening after intra-uterine exposure to ETI von De Wachter, E, Davies, JC, Simmonds, NJ, Castellani, C, de Winter-de Groot, KM, Munck, A, Proesmans, M, Southern, KW, Barben, J

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Phenotypic characterisation of patients with intermediate sweat chloride values: towards validation of the European diagnostic algorithm for cystic fibrosis von Goubau, C, Wilschanski, M, Skalická, V, Lebecque, P, Southern, K W, Sermet, I, Munck, A, Derichs, N, Middleton, P G, Hjelte, L, Padoan, R, Vasar, M, De Boeck, K

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Azithromycin for cystic fibrosis von Southern, K.W, Barker, P.M

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Assessing the Liverpool Respiratory Symptom Questionnaire in children with cystic fibrosis von TRINICK, R, SOUTHERN, K. W, MCNAMARA, P. S

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Repeat administration of DNA/liposomes to the nasal epithelium of patients with cystic fibrosis von HYDE, S. C, SOUTHERN, K. W, EGAN, J. J, SORGI, F. L, HUANG, L, CUTHBERT, A. W, EVANS, M. J, COLLEDGE, W. H, HIGGINS, C. F, WEBB, A. K, GILL, D. R, GILEADI, U, FITZJOHN, E. M, MOFFORD, K. A, WADDELL, B. E, GOOI, H. C, GODDARD, C. A, HANNAVY, K, SMYTH, S. E

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A European consensus for the evaluation and management of infants with an equivocal diagnosis following newborn screening for cystic fibrosis von Mayell, S.J, Munck, A, Craig, J.V, Sermet, I, Brownlee, K.G, Schwarz, M.J, Castellani, C, Southern, K.W

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Cystic Fibrosis Screen Positive, Inconclusive Diagnosis (CFSPID): A new designation and management recommendations for infants with an inconclusive diagnosis following newborn scre... von Munck, A, Mayell, S.J, Winters, V, Shawcross, A, Derichs, N, Parad, R, Barben, J, Southern, K.W

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Topical cystic fibrosis transmembrane conductance regulator gene replacement for cystic fibrosis-related lung disease von Perry, LA, Penny-Dimri, JC, Aslam, AA, Lee, TW, Southern, KW

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International approaches for delivery of positive newborn bloodspot screening results for CF von Chudleigh, J, Ren, C.L, Barben, J, Southern, K.W

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Recommendations for the classification of diseases as CFTR-related disorders von Bombieri, C, Claustres, M, De Boeck, K, Derichs, N, Dodge, J, Girodon, E, Sermet, I, Schwarz, M, Tzetis, M, Wilschanski, M, Bareil, C, Bilton, D, Castellani, C, Cuppens, H, Cutting, G.R, Drevínek, P, Farrell, P, Elborn, J.S, Jarvi, K, Kerem, B, Kerem, E, Knowles, M, Macek, M, Munck, A, Radojkovic, D, Seia, M, Sheppard, D.N, Southern, K.W, Stuhrmann, M, Tullis, E, Zielenski, J, Pignatti, P.F, Ferec, C

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Inconclusive diagnosis after a positive newborn bloodspot screening result for cystic fibrosis; clarification of the harmonised international definition von Southern, K.W., Barben, J., Gartner, S., Munck, A., Castellani, C., Mayell, S.J., Davies, J.C., Winters, V., Murphy, J., Salinas, D., McColley, S.A., Ren, C.L., Farrell, P.M.

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A placebo-controlled study of liposome-mediated gene transfer to the nasal epithelium of patients with cystic fibrosis von GILL, D. R, SOUTHERN, K. W, LANE, D. J, LITTLEWOOD, J. M, WEBB, A. K, MIDDLETON, P. G, COLLEDGE, W. H, CUTHBERT, A. W, EVANS, M. J, HIGGINS, C. F, HYDE, S. C, MOFFORD, K. A, SEDDON, T, HUANG, L, SORGI, F, THOMSON, A, MACVINISH, L. J, RATCLIFF, R, BILTON, D

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Standards of care guidance for sweat testing; phase two of the ECFS quality improvement programme von Cirilli, N., Southern, K.W., Barben, J., Vermeulen, F., Munck, A., Wilschanski, M., Nguyen-Khoa, Thao, Aralica, M., Simmonds, NJ, De Wachter, E.

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A systematic cochrane review of corrector therapies (with or without potentiators) for people with cystic fibrosis with class II gene variants (most commonly F508DEL) [1] von Southern, K.W., Murphy, J., Sinha, I.P., Nevitt, S.J.

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A survey of palivizumab for infants with cystic fibrosis in the UK von McCormick, J, Southern, K W

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A systematic Cochrane Review of autogenic drainage (AD) for airway clearance in cystic fibrosis von McCormack, P., Burnham, P., Southern, K.W.

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ECFS standards of care on CFTR-related disorders: Identification and care of the disorders von Simmonds, N.J., Southern, K.W., De Wachter, E., De Boeck, K., Bodewes, F., Mainz, J.G., Middleton, P.G., Schwarz, C., Vloeberghs, V., Wilschanski, M., Bourrat, E., Chalmers, J.D., Ooi, C.Y., Debray, D., Downey, D.G., Eschenhagen, P., Girodon, E., Hickman, G., Koitschev, A., Nazareth, D., Nick, J.A., Peckham, D., VanDevanter, D., Raynal, C., Scheers, I., Waller, M.D., Sermet-Gaudelus, I., Castellani, C.

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Real life practice of sweat testing in Europe von Cirilli, N., Southern, K.W., Buzzetti, R., Barben, J., Nährlich, L., Munck, A., Wilschanski, M., De Boeck, K., Derichs, N.

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