Select Publications
Journal articles
2003, 'Urokinase in the treatment of childhood empyema [5] (multiple letters)', Thorax, 58, pp. 93 - 94, http://dx.doi.org/10.1136/thorax.58.1.93
,2002, 'Are annual blood tests in preschool cystic fibrosis patients worthwhile?', Archives of Disease in Childhood, 87, pp. 518 - 520, http://dx.doi.org/10.1136/adc.87.6.518
,2002, 'Macrolides in the respiratory tract in cystic fibrosis', Journal of the Royal Society of Medicine, Supplement, 95, pp. 27 - 31
,2002, 'Treatment of severe small airways disease in children with cystic fibrosis: Alternatives to corticosteroids', Pediatric Drugs, 4, pp. 381 - 389, http://dx.doi.org/10.2165/00128072-200204060-00005
,2001, 'The anti-inflammatory effects of macrolides in cystic fibrosis', Japanese Journal of Antibiotics, 54, pp. 77 - 82
,2001, 'Routine ventilation scans in children with cystic fibrosis: Diagnostic usefulness and prognostic value', European Journal of Nuclear Medicine, 28, pp. 1313 - 1318, http://dx.doi.org/10.1007/s002590100573
,2001, 'Anti-inflammatory effects of macrolides in lung disease', Pediatric Pulmonology, 31, pp. 464 - 473, http://dx.doi.org/10.1002/ppul.1076
,2001, 'Cystic fibrosis: Review of the decade', Monaldi Archives for Chest Disease, 56, pp. 240 - 247
,2001, 'Genetic contributions to rare childhood lung diseases', Paediatric Respiratory Reviews, 2, pp. 268 - 275, http://dx.doi.org/10.1053/prrv.2001.0150
,2001, 'Health effects of air pollution exposure on children and adolescents in São Paulo, Brazil', Pediatric Pulmonology, 31, pp. 106 - 113, http://dx.doi.org/10.1002/1099-0496(200102)31:2<106::AID-PPUL1017>3.0.CO;2-M
,2000, 'Confirmation of abnormal chloride ion secretion in the lower airway of children with cystic fibrosis', Thorax, 55
,2000, 'Cationic lipid-mediated gene transfer to the growing murine and human airway', Gene Therapy, 7, pp. 273 - 278, http://dx.doi.org/10.1038/sj.gt.3301091
,1999, 'Corticosteroid insensitive asthma in children', Thorax, 54
,1999, 'If you can't stand the rash, get out of the kitchen: An unusual adverse reaction to ciprofloxacin', Pediatric Pulmonology, 28, pp. 449 - 450, http://dx.doi.org/10.1002/(SICI)1099-0496(199912)28:6<449::AID-PPUL11>3.0.CO;2-H
,1999, 'Cationic lipid-mediated CFTR gene transfer to the lungs and nose of patients with cystic fibrosis: A double-blind placebo-controlled trial', Lancet, 353, pp. 947 - 954, http://dx.doi.org/10.1016/S0140-6736(98)06532-5
,1999, 'Pulmonary disease severity in men with ΔF508 cystic fibrosis and residual chloride secretion', Lancet, 353, pp. 984 - 985, http://dx.doi.org/10.1016/S0140-6736(98)05447-6
,1999, 'Cystic fibrosis: A management update', Prescribers' Journal, 39, pp. 91 - 96
,1999, 'Prospects for gene therapy in cystic fibrosis', Archives of Disease in Childhood, 80, pp. 286 - 289, http://dx.doi.org/10.1136/adc.80.3.286
,1999, 'The in vivo effects of milrinone on the airways of cystic fibrosis mice and human subjects', American Journal of Respiratory Cell and Molecular Biology, 20, pp. 129 - 134, http://dx.doi.org/10.1165/ajrcmb.20.1.3278
,1998, 'Cationic lipid-mediated gene transfer to the growing murine airway', Thorax, 53
,1998, 'Comparison of the active cycle of breathing techniques and external high frequency oscillation jacket for clearance of secretions in children with cystic fibrosis', Thorax, 53
,1998, 'Long-term azithromycin may improve lung function in children with cystic fibrosis', Lancet, 351, pp. 420, http://dx.doi.org/10.1016/S0140-6736(05)78360-4
,1998, 'Distal 10q trisomy syndrome with unusual cardiac and pulmonary abnormalities', Journal of Medical Genetics, 35, pp. 72 - 74, http://dx.doi.org/10.1136/jmg.35.1.72
,1997, 'A double blind placebo controlled trial of pulmonary and nasal administration of liposome-mediated CFTR gene transfer in CF subjects', Thorax, 52
,1997, 'Long term azithromycin improves lung function in children with cystic fibrosis', Thorax, 52
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