Verfügbarkeit: Cystic fibrosis

Cystic fibrosis:

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Bibliographische Detailangaben
Format:	Buch
Sprache:	English
Veröffentlicht:	London [u.a.] Hodder Arnold 2007
Ausgabe:	3. ed.
Schlagworte:	Kystische fibrose Cystic Fibrosis Cystic fibrosis Mukoviszidose Aufsatzsammlung
Online-Zugang:	Inhaltsverzeichnis
Beschreibung:	Literaturangaben
Beschreibung:	XI, 503 S. Ill., graph. Darst.

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Datensatz im Suchindex

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adam_text	Contents Color plates appear between pages 259 and 260. Contributors ix Preface xiii PART 1 INTRODUCTION: WHAT IS CYSTIC FIBROSIS? 1 History of cystic fibrosis 3 James M. Littlewood 2 Epidemiology of cystic fibrosis 21 Sarah Walters and Anil Mehta PART 2 BASIC SCIENCE FOR THE CLINICIAN 3 Molecular biology of cystic fibrosis: CFTR processing and functions, and classes of mutations 49 Malka Nissim Rafinia, Batsheva Kerem and Eitan Kerem 4 Pathophysiology: epithelial cell biology and ion channel function in the lung, sweat gland and pancreas 59 Raymond D. Coakley and Richard C Boucher 5 Immunology of cystic fibrosis 69 Gerd Doring and Felix Ratjen 6a Genotype phenotype correlations and modifier genes 81 Jane C. Davies 6b Variability of clinical course in cystic fibrosis 87 Michael Schechter PART 3 DIAGNOSTIC ASPECTS OF CYSTIC FIBROSIS 7 Diagnosis of cystic fibrosis 99 Colin Wallis 8a The challenge of screening newborn infants for cystic fibrosis 109 Kevin W. Southern 8b How to manage the screened patient 117 Philip Robinson 9 Microbiology of cystic fibrosis: role of the clinical microbiology laboratory, susceptibility and 123 synergy studies and infection control Samiya Razvi and Lisa Saiman PART 4 CLINICAL ASPECTS OF CYSTIC FIBROSIS 10 Respiratory disease: infection 137 Ian M. Balfour Lynn andJ. Stuart Elborn 11 Respiratory disease: non infectious complications 159 Margaret Hodson and Andrew Bush 12 Sleep, lung mechanics and work of breathing, including NIPPV 175 Brigitte Fauroux andAnnick Clement 13 Delivery of therapy to the cystic fibrosis lung 185 Harm A. W. M. Tiddens and Sunalene G. Devadason 14 The upper airway in cystic fibrosis 199 William £ Grant 15a Gastrointestinal disease in cystic fibrosis 209 Ian Gooding and David Westaby 15b Liver, biliary and pancreatic disease 225 Vicky Dondos and David Westaby 16 Insulin deficiency and diabetes related to cystic fibrosis 241 Christopher D. Sheldon and Lee Dobson 17 Growth and puberty 253 Nicola Bridges 18 Cystic fibrosis related low bone mineral density 261 Sarah L Elkin and Charles S. Haworth 19 Other system disorders in cystic fibrosis 269 Khin Ma Gyi 20 Sexual and reproductive health 279 Susan M. Sawyer 21 Transplantation 291 Paul Aurora, Khin Gyi and Martin Carby PART 5 MONITORING 22 Using databases to improve care 311 Sheila G. McKenzie and Margaret £ Hodson 23a Infant and pre school children: lung function 321 Sarath Ranganathan 23b Infant and pre school children: role of bronchoscopy 331 Gary Connett 23c Infant and pre school children: imaging the lungs 337 Samatha Sonnappa and Catherine M. Owens 24 Physiological monitoring of older children and adults 345 Mark Rosenthal 25a Exercise: testing 353 David M. Orenstein and Wolfgang Gruber 25b Exercise: use in therapy 361 David M. Orenstein and Linda W. Higgins 26 Clinical outcome measures to assess new treatments for CF lung disease 375 Jane C. Davies and Eric W.F.W. Alton on behalf of the UK CF Gene Therapy Consortium PART 6 MULTIDISCIPLINARY CARE 27 Cystic fibrosis center care 387 Penny Agent and Susan Madge 28 Nursing care 399 Susan Madge and Christine Hockings 29 Physiotherapy 407 Craig Lapin, Anne Lapin and Jennifer A. Pryor 30 Nutritional aspects 421 Sue Wolfe and Sarah Collins 31 Psychological aspects of cystic fibrosis 431 AlistairJ. A. Duff and Helen Oxley 32 Palliative care in cystic fibrosis 441 Catherine £ Urch and Margaret £ Hodson PART 7 CYSTIC FIBROSIS: THE FUTURE 33a Gene and stem cell therapy 453 Uta Griesenbach and Eric W. F. W. Alton on behalf of the UK CF Gene Therapy Consortium 33b Non gene therapy treatments: what will they deliver? 463 Adam Jaffe and Pierre Barker 34 The future: how will management change? 471 Andrew Bush and Duncan Geddes APPENDICES Appendix 1 Transition form 479 Susan Madge and Jacqueline Francis Appendix 2 Practical nursing care required by the cystic fibrosis patient and its delivery 483 Frances Duncan Skingle and Tracey Catling Index 487
adam_txt	Contents Color plates appear between pages 259 and 260. Contributors ix Preface xiii PART 1 INTRODUCTION: WHAT IS CYSTIC FIBROSIS? 1 History of cystic fibrosis 3 James M. Littlewood 2 Epidemiology of cystic fibrosis 21 Sarah Walters and Anil Mehta PART 2 BASIC SCIENCE FOR THE CLINICIAN 3 Molecular biology of cystic fibrosis: CFTR processing and functions, and classes of mutations 49 Malka Nissim Rafinia, Batsheva Kerem and Eitan Kerem 4 Pathophysiology: epithelial cell biology and ion channel function in the lung, sweat gland and pancreas 59 Raymond D. Coakley and Richard C Boucher 5 Immunology of cystic fibrosis 69 Gerd Doring and Felix Ratjen 6a Genotype phenotype correlations and modifier genes 81 Jane C. Davies 6b Variability of clinical course in cystic fibrosis 87 Michael Schechter PART 3 DIAGNOSTIC ASPECTS OF CYSTIC FIBROSIS 7 Diagnosis of cystic fibrosis 99 Colin Wallis 8a The challenge of screening newborn infants for cystic fibrosis 109 Kevin W. Southern 8b How to manage the screened patient 117 Philip Robinson 9 Microbiology of cystic fibrosis: role of the clinical microbiology laboratory, susceptibility and 123 synergy studies and infection control Samiya Razvi and Lisa Saiman PART 4 CLINICAL ASPECTS OF CYSTIC FIBROSIS 10 Respiratory disease: infection 137 Ian M. Balfour Lynn andJ. Stuart Elborn 11 Respiratory disease: non infectious complications 159 Margaret Hodson and Andrew Bush 12 Sleep, lung mechanics and work of breathing, including NIPPV 175 Brigitte Fauroux andAnnick Clement 13 Delivery of therapy to the cystic fibrosis lung 185 Harm A. W. M. Tiddens and Sunalene G. Devadason 14 The upper airway in cystic fibrosis 199 William £ Grant 15a Gastrointestinal disease in cystic fibrosis 209 Ian Gooding and David Westaby 15b Liver, biliary and pancreatic disease 225 Vicky Dondos and David Westaby 16 Insulin deficiency and diabetes related to cystic fibrosis 241 Christopher D. Sheldon and Lee Dobson 17 Growth and puberty 253 Nicola Bridges 18 Cystic fibrosis related low bone mineral density 261 Sarah L Elkin and Charles S. Haworth 19 Other system disorders in cystic fibrosis 269 Khin Ma Gyi 20 Sexual and reproductive health 279 Susan M. Sawyer 21 Transplantation 291 Paul Aurora, Khin Gyi and Martin Carby PART 5 MONITORING 22 Using databases to improve care 311 Sheila G. McKenzie and Margaret £ Hodson 23a Infant and pre school children: lung function 321 Sarath Ranganathan 23b Infant and pre school children: role of bronchoscopy 331 Gary Connett 23c Infant and pre school children: imaging the lungs 337 Samatha Sonnappa and Catherine M. Owens 24 Physiological monitoring of older children and adults 345 Mark Rosenthal 25a Exercise: testing 353 David M. Orenstein and Wolfgang Gruber 25b Exercise: use in therapy 361 David M. Orenstein and Linda W. Higgins 26 Clinical outcome measures to assess new treatments for CF lung disease 375 Jane C. Davies and Eric W.F.W. Alton on behalf of the UK CF Gene Therapy Consortium PART 6 MULTIDISCIPLINARY CARE 27 Cystic fibrosis center care 387 Penny Agent and Susan Madge 28 Nursing care 399 Susan Madge and Christine Hockings 29 Physiotherapy 407 Craig Lapin, Anne Lapin and Jennifer A. Pryor 30 Nutritional aspects 421 Sue Wolfe and Sarah Collins 31 Psychological aspects of cystic fibrosis 431 AlistairJ. A. Duff and Helen Oxley 32 Palliative care in cystic fibrosis 441 Catherine £ Urch and Margaret £ Hodson PART 7 CYSTIC FIBROSIS: THE FUTURE 33a Gene and stem cell therapy 453 Uta Griesenbach and Eric W. F. W. Alton on behalf of the UK CF Gene Therapy Consortium 33b Non gene therapy treatments: what will they deliver? 463 Adam Jaffe and Pierre Barker 34 The future: how will management change? 471 Andrew Bush and Duncan Geddes APPENDICES Appendix 1 Transition form 479 Susan Madge and Jacqueline Francis Appendix 2 Practical nursing care required by the cystic fibrosis patient and its delivery 483 Frances Duncan Skingle and Tracey Catling Index 487
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spellingShingle	Cystic fibrosis Kystische fibrose gtt Cystic Fibrosis Cystic fibrosis Mukoviszidose (DE-588)4040669-6 gnd
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title	Cystic fibrosis
title_auth	Cystic fibrosis
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