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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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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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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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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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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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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Risk-benefit experience of ciprofloxacin use in pediatric patients in the United Kingdom von Redmond, A O

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

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Clinical and pharmacokinetic aspects of ciprofloxacin in the treatment of acute exacerbations of pseudomonas infection in cystic fibrosis patients von Steen, H. J., Scott, E. M., Stevenson, M. I., Black, A. E., Redmond, A. O. B., Collier, P. S.

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

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Detection of cystic fibrosis homozygotes and heterozygotes by serum isoelectrofocusing von Nevin, G B, Nevin, N C, Redmond, A O, Young, I R, Tully, G W

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Cystic fibrosis in Northern Ireland von Nevin, G B, Nevin, N C, Redmond, A O

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The colon in kwashiorkor von Redmond, A. O. B., Kaschula, R. O. C., Freeseman, C., Hansen, J. D. L.

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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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Prevalence and survival of patients with cystic fibrosis in Northern Ireland, 1961-1971 von Nevin, G B, Nevin, N C, Redmond, A O

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Hypothalamic tumour presenting as anorexia nervosa von McClean, P, Redmond, A O

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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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Renal tubular acidosis with nerve deafness von McShane, M A, Carson, D J, Redmond, A O, Adams, D

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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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