JA Innes
- Laboratory assessment of fitness to fly in patients with lung disease: a practical approachBy AG Robson, TK Hartung and JA InnesAG RobsonTK Hartung
- Correlation between nasal potential difference measurements, genotype and clinical condition in patients with cystic fibrosisBy LP Ho, JM Samways, DJ Porteous, Dorin, A Carothers, AP Greening and JA InnesLP HoJM SamwaysDJ PorteousDorin JRA CarothersAP Greening
- Expired hydrogen peroxide in breath condensate of cystic fibrosis patientsBy LP Ho, J Faccenda, JA Innes and AP GreeningLP HoJ FaccendaJA Innes
- Recombinant DNase in cystic fibrosis: a protocol for targeted introduction through n-of-1 trials. Scottish Cystic Fibrosis GroupBy FG Bollert, JY Paton, TG Marshall, J Calvert, AP Greening and JA InnesFG BollertJY PatonTG MarshallJ CalvertAP Greening
- Totally implantable venous access devices in cystic fibrosis: complications and patients' opinionsBy HC Rodgers, K Liddle, SJ Nixon, JA Innes and AP GreeningHC RodgersK LiddleSJ NixonJA Innes
- Exhaled nitric oxide is not elevated in the inflammatory airways diseases of cystic fibrosis and bronchiectasisBy LP Ho, JA Innes and AP GreeningLP HoJA Innes
- The current single exhalation method of measuring exhales nitric oxide is affected by airway calibreBy LP Ho, FT Wood, A Robson, JA Innes and AP GreeningLP HoFT WoodA RobsonJA Innes
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About the ERS books
The ERS Monograph is the quarterly book series from the European Respiratory Society. Each Monograph covers a specific area of respiratory medicine, providing in-depth reviews that give clinicians at all levels a concise, comprehensive guide to symptoms, diagnosis and treatment.
The ERS Handbooks are compact guides to broad areas of the respiratory field. Launched in 2010, the series now covers adult, paediatric and sleep respiratory medicine, includes a companion volume of self-assessment questions and features the ERS Practical Handbooks.