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Aslam, AA, Higgins, C, Sinha, IP and Southern, KW ORCID: 0000-0001-6516-9083
(2017)
Ataluren and similar compounds (specific therapies for premature termination codon class I mutations) for cystic fibrosis.
The Cochrane database of systematic reviews, 1 (1).
pp. 1-20.
Neill, DR ORCID: 0000-0002-7911-8153, Saint, GL ORCID: 0000-0003-4031-4939, Bricio-Moreno, L, Fothergill, J ORCID: 0000-0002-7012-1508, Southern, KW ORCID: 0000-0001-6516-9083, Winstanley, C ORCID: 0000-0002-2662-8053, Christmas, SE, Slupsky, JR ORCID: 0000-0002-7410-9004, McNamara, PS ORCID: 0000-0002-7055-6034, Kadioglu, A ORCID: 0000-0003-1137-6321 et al (show 1 more authors)
(2014)
THE B LYMPHOCYTE DIFFERENTIATION FACTOR (BAFF) IS EXPRESSED IN THE AIRWAYS OF CHILDREN WITH CF AND IN LUNGS OF MICE INFECTED WITH PSEUDOMONAS AERUGINOSA.
PLoS One, 9 (5).
e95892-.
Munck, A, Mayell, SJ, Winters, V, Shawcross, A, Derichs, N, Parad, R, Barben, J and Southern, KW ORCID: 0000-0001-6516-9083
(2015)
Cystic Fibrosis Screen Positive, Inconclusive Diagnosis (CFSPID): A new designation and management recommendations for infants with an inconclusive diagnosis following newborn screening.
Journal of Cystic Fibrosis, 14 (6).
pp. 706-713.
Southern, KW ORCID: 0000-0001-6516-9083, Barben, J, Gartner, S, Munck, A, Castellani, C, Mayell, SJ, Davies, JC, Winters, V, Murphy, J, Salinas, D et al (show 3 more authors)
(2019)
Inconclusive diagnosis after a positive newborn bloodspot screening result for cystic fibrosis; clarification of the harmonised international definition.
JOURNAL OF CYSTIC FIBROSIS, 18 (6).
pp. 778-780.
Chudleigh, J, Ren, CL, Barben, J and Southern, KW ORCID: 0000-0001-6516-9083
(2019)
International approaches for delivery of positive newborn bloodspot screening results for CF.
JOURNAL OF CYSTIC FIBROSIS, 18 (5).
pp. 614-621.
Castellani, C, Massie, J, Sontag, M and Southern, KW ORCID: 0000-0001-6516-9083
(2016)
Newborn screening for cystic fibrosis.
The Lancet Respiratory Medicine, 4 (8).
pp. 653-661.
Cirilli, N, Southern, KW ORCID: 0000-0001-6516-9083, Buzzetti, R, Barben, J, Nahrlich, L, Munck, A, Wilschanski, M, De Boeck, K, Derichs, N and Working, ECFS Diagnostic Network
(2018)
Real life practice of sweat testing in Europe.
JOURNAL OF CYSTIC FIBROSIS, 17 (3).
pp. 325-332.
Pybus, S
(2016)
Skin microbiome of children with cystic fibrosis.
Master of Philosophy thesis, University of Liverpool.
Cirilli, N, Southern, KW ORCID: 0000-0001-6516-9083, Barben, J, Vermeulen, F, Munck, A, Wilschanski, M, Nguyen-Khoa, Thao, Aralica, M, Simmonds, NJ and De Wachter, E
(2022)
Standards of care guidance for sweat testing; phase two of the ECFS quality improvement programme.
Journal of Cystic Fibrosis, 21 (1).
pp. 434-441.
Perry, LA, Penny-Dimri, JC, Aslam, AA, Lee, TW and Southern, KW ORCID: 0000-0001-6516-9083
(2017)
Topical cystic fibrosis transmembrane conductance regulator gene replacement for cystic fibrosis-related lung disease.
PAEDIATRIC RESPIRATORY REVIEWS, 22.
pp. 47-49.
Perry, LA, Penny-Dimri, JC, Aslam, AA, Lee, TW and Southern, KW ORCID: 0000-0001-6516-9083
(2017)
Topical cystic fibrosis transmembrane conductance regulator gene replacement for cystic fibrosis-related lung disease.
Paediatric respiratory reviews, 22.
pp. 47-49.
Barben, J, Winters, V, Castellani, C, Dankert-Roelse, J, Gartner, S, Kashirskaya, N, Linnane, B, Munck, A, Sands, D, Sommerburg, O et al (show 1 more authors)
(2016)
UPDATED SURVEY OF NEWBORN SCREENING FOR CYSTIC FIBROSIS IN EUROPE.
.
Schlüter, DK, Dryden, C, Southern, KW, Diggle, PJ and Taylor-Robinson, D
(2018)
WS05.1 Impact of newborn screening on outcomes and social inequalities in cystic fibrosis: a UK Registry-based study.
.
McCormack, P, Burnham, P and Southern, KW ORCID: 0000-0001-6516-9083
(2019)
A systematic Cochrane Review of autogenic drainage (AD) for airway clearance in cystic fibrosis.
, England.