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£34.99
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Cystic Fibrosis
Edited by Alex Horsley, Steve Cunningham, and Alistair Innes
192 pages
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numerous black-and-white line drawings and photographs
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180x100mm
978-0-19-958270-9
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Paperback
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16 September 2010
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- Helpful Key Points at the beginning of each chapter to summarise content
- Portable, accessible format for quick reference
- Includes up-to-date research literature that has direct clinical application for busy healthcare professionals
Cystic fibrosis is the most common life-threatening inherited disease in the UK and Europe. It affects around 1 in 2500 live births in the UK. There have been enormous advances in the treatment of CF over the last 40 years, with life expectancy increasing from just 5 years in 1964 to mid 30s today, and it now affects as many adults as children. The burden of care for CF patients is, however, considerable, and with the increase in life expectancy the impact of CF on respiratory medicine has increased considerably. Part of the Oxford Respiratory Medicine Library series, this pocketbook aims to be a
concise companion for all health care professionals who manage, or come across, patients with CF. The book covers all aspects of care, including both paediatric and adult-specific issues. The book will appeal to a wide variety of health professionals in respiratory medicine, paediatrics, and primary care.Readership: The book will appeal to a wide variety of health professionals in respiratory medicine, paediatrics, and primary care.
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Edited by Alex Horsley, Senior Fellow, Manchester Adult CF Centre, University Hospitals South Manchester, Wythenshawe Hospital, Manchester, UK, Steve Cunningham, Consultant Respiratory Paediatrician & Part Time Senior Lecturer, Department of Child Life & Health, Royal Hospital for Sick Children, Edinburgh, UK, and Alistair Innes, Consultant Physician and Honorary Reader in Respiratory Medicine Scottish Adult CF Service, Western General Hospital, Edinburgh, UK Contributors: Eric Alton, Professor of Respiratory Medicine and Gene Therapy, Honorary Consultant Physician at the Royal Brompton and Harefield
Hospital, Department of Gene Therapy, National Heart & Lung Institute, Imperial College, London, UK Sally Connolly, Consultant Paediatrician, Sheffield Children's Hospital, Sheffield, UK Steve Cunningham, Consultant Respiratory Paediatrician & Part Time Senior Lecturer, Department of Child Life & Health, Royal Hospital for Sick Children, Edinburgh, UK Jane Davies, Reader in Paediatric Respiratory Medicine and Gene Therapy, Honorary Consultant at the Royal Brompton and Harefield Hospital, National Heart & Lung Institute, Imperial College, London, UK Gerd Döring, Professor and Head of Cystic Fibrosis Research Group, Institute of Medical Microbiology and Hygiene, University of Tübingen, Tübingen, Germany Alistair Duff, Consultant
Clinical Psychologist & Honorary Senior Lecturer, Head of Psychology Services, Leeds Teaching Hospitals & Leeds University School of Medicine, Leeds, UK Frank Edenborough, Consultant Respiratory Physician and Clinical Lead, Sheffield Adult CF Centre, Northern General Hospital, Sheffield, UK Andrew J Fisher, Professor of Respiratory Transplant Medicine & Honorary Consultant Chest Physician, Cardiopulmonary Transplant Unit, Freeman Hospital, Newcastle Upon Tyne, UK Uta Griesenbach, Reader in Molecular Medicine, National Heart & Lung Institute, Imperial College, London, UK Charles Haworth, Consultant Respiratory Physician, Adult Cystic Fibrosis Centre and Lung Defence Unit, Papworth Hospital, Cambridge, UK Alex Horsley, Senior
Fellow, Manchester Adult CF Centre, University Hospitals South Manchester, Wythenshawe Hospital, Manchester, UK J Alastair Innes, Consultant Physician and Honorary Reader in Respiratory Medicine, Scottish Adult CF Service, Western General Hospital, Edinburgh, UK Antoinette Moran, Division Chief & Professor of Paediatric Endocrinology, University of Minnesota, Minneapolis, USA Stephen O'Riordan, Clinician Researcher in Diabetes, Endocrinology and CFRD, The Institute of Child Health & Great Ormond Street Hospital, London, UK Helen Oxley, Consultant Clinical Psychologist, Manchester Adult CF Centre, Wythenshawe Hospital, Manchester, UK Manchester, UK Laura Tanner, Specialist Registrar in Respiratory Medicine, Cardiopulmonary Transplant Unit,
Freeman Hospital, Newcastle Upon Tyne, UK Christopher Taylor, Professor of Paediatric Gastroenterology, Academic Unit of Child Health, University of Sheffield, Sheffield, UK Dieter Worlitzsch, Senior Physician & Specialist for Hygiene and Environmental Medicine, Institute of Hygiene, University Hospital of Halle, Halle, Germany
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1: Alex Horsley: Genetics and pathophysiology
2: Steve Cunningham: Diagnosis and process of care
3: Gerd Döring and Dieter Worlitzsch: Microbiology of CF lung disease
4: J. Alastair Innes: Management of stable CF lung disease
5: Alex Horsley: Management of respiratory exacerbations
6: Christopher Taylor and Sally Connolly: Gastrointestinal disease and nutrition
7: Stephen M. P. O'Riordan and Antoinette Moran: Cystic fibrosis related diabetes
8: Charles Haworth: Metabolic and musculoskeletal effects
9: Alistair J.A. Duff and Helen Oxley: Psychosocial aspects of CF care
10: Laura Tanner and Andrew J. Fisher: Lung transplantation
11: Frank P. Edenborough: Fertility, contraception and pregnancy
12: Uta Griesenbach, Jane C. Davies, and Eric W.F.W. Alton: Future treatments
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The specification in this catalogue, including without limitation price, format, extent, number of illustrations, and month of publication, was as accurate as possible at the time the catalogue was compiled. Occasionally, due to the nature of some contractual restrictions, we are unable to ship a specific product to a particular territory. Jacket images are provisional and liable to change before publication.
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