A review of cystic fibrosis children born to single mothers von Macpherson, C, Redmond, AOB, Leavy, A, McMullan, M

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Energy balance in cystic fibrosis when stable and during a respiratory exacerbation von Mc Closkey, Margaret, Redmond, Aileen O.B., Mc Cabe, Christine, Pyper, Siobhan, Westerterp, Klass R., Elborn, Stuart J.

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Risk Factors for Early Acquisition of Pseudomonas Aeruginosa Endobronchial Infection in Cystic Fibrosis (CF) Children von Reid, AJM, McCaughen, J, Shields, M D, Redmond, AOB

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Clinical outcome after acquisition of Burkholderia Cepacia in Cystic Fibrosis von Mc Closkey, M, Mc Caughen, J, Redmond, AOB, Elborn, J S

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Clinical Features Associated with a Delayed Diagnosis of Cystic Fibrosis von McCloskey, M., Redmond, A.O.B., Hill, A., Elborn, J.S.

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Antibiotic resistance in Burkholderia cepacia at two regional cystic fibrosis centres in Northern Ireland: is there a need for synergy testing? von Moore, John E., Crowe, Mary, Shaw, Adrienne, McCaughan, John, Redmond, Aileen O. B., Elborn, J. Stuart

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Total energy expenditure in stable patients with cystic fibrosis von McCLOSKEY, M., REDMOND, A.O.B., PYPER, S., McCABE, C., WESTERTERP, K.R., ELBORN, J.S.

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Resource allocation trade-offs in a mast-seeding conifer: piñon pine prioritizes reproduction over defence von Redmond, Miranda D, Davis, Thomas Seth, Ferrenberg, Scott, Wion, Andreas P

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Improved cultural detection of Burkholderia cepacia from sputum in patients with cystic fibrosis von Wright, R M, Moore, J E, Shaw, A, Dunbar, K, Dodd, M, Webb, K, Redmond, A O B, Crowe, M, Murphy, P G, Peacock, S, Elborn, J S

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Misidentification of a genomovar of Burkholderia cepacia by recA restriction fragment length polymorphism von Moore, J E, Millar, B C, Xu, J, Crowe, M, Redmond, A O B, Elborn, J S

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Burkholderia cepacia from a sink drain von Moore, J.E., Thompson, I., Crowe, M., Xu, J., Shaw, A., Millar, B.C., Redmond, A.O.B., Reid, A.J.M., Clarke, C., Elborn, J.S.

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Molecular (PCR) detection of Pseudomonas spp. other than P. aeruginosa directly from the sputum of adults and children with cystic fibrosis von Xu, J., Moore, J.E., Murphy, P.G., Millar, B.C., Redmond, A.O.B., Elborn, J.S.

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GENOTYPE IDENTIFICATION CHARACTERISED BY VARIATION IN BASAL METABOLIC RATE IN CYSTIC FIBROSIS von O'Rawe, A, Dodge, J A, Redmond, AOB, McIntosh, I, Brock, DJH

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GENOTYPE IDENTIFICATION CHARACTERISED BY VARIATION IN BASAL METABOLIC RATE IN CYSTIC FIBROSIS von OʼRawe, A, Dodge, J A, Redmond, AOB, McIntosh, I, Brock, DJH

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Retransplantation in a patient with cystic fibrosis von McCloskey, M, Maxwell, A P, Hall, V, Redmond, A O B, Elborn, J S

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Tolerance and safety of ciprofloxacin in paediatric patients von Black, A., Redmond, A. O. B., Steen, H. J., Oborska, I. T.

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Low incidence of Neisseria meningitidis serogroups B and C in lower respiratory tract secretions in patients with cystic fibrosis von Dunbar, K, Moore, J E, Xu, J, Devine, M, Murphy, P G, Redmond, A O B, Elborn, J S

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An unusual cause of thoracic mass von Wilson, D C, Redmond, A O

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Comparison between a standard pancreatic supplement and a high enzyme preparation in cystic fibrosis von MORRISON, G., MORRISON, J. M., REDMOND, A. O. B., BYERS, C. A., McCRACKEN, K. J., DODGE, J. A., GUILFORDS, S. A., BOWDEN, M. W.

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Gene/energy interaction in cystic fibrosis von O'Rawe, A., Dodge, J.A., Redmond, A.O.B., Mcintosh, I., Brock, D.J.H.

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