Cystic fibrosis / / edited by Julian L. Allen, Howard B. Panitch, and Ronald C. Rubenstein |
Pubbl/distr/stampa | New York, N.Y. : , : Informa Healthcare USA, , 2010 |
Descrizione fisica | 1 online resource (546 p.) |
Disciplina | 616.3/72 |
Altri autori (Persone) |
AllenJulian Lewis
RubensteinRonald PanitchHoward B |
Collana | Lung biology in health and disease |
Soggetto topico |
Cystic fibrosis
Lungs - Diseases |
Soggetto genere / forma | Electronic books. |
ISBN |
0-429-06998-7
1-282-56094-8 9786612560941 1-4398-0182-7 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
Front Cover; Preface; Contents; Chapter 1. The Genetics of Cystic Fibrosis; Chapter 2. Ion Transport; Chapter 3. Mucus Abnormalities and Ciliary Dysfunction; Chapter 4. Microbiology in Cystic Fibrosis; Chapter 5. Inflammation in the Cystic Fibrosis Lung; Chapter 6. Modifier Genes of Cystic Fibrosis; Chapter 7. Cystic Fibrosis: Diagnosis, Sweat Testing, and Newborn Screening; Chapter 8. Diagnostic Approach to Diseases Associated with Cystic Fibrosis Transmembrane Conductance Regulator Gene Mutations; Chapter 9. Lung Function Testing in Infants
Chapter 10. Assessment of Lung Function in Young Children with Cystic FibrosisChapter 11. Lung Function Testing in School-Age Children with Cystic Fibrosis; Chapter 12. Thoracic Imaging in Cystic Fibrosis Pulmonary Disease; Chapter 13. Pulmonary Manifestations; Chapter 14. Treatment Strategies for Maintaining Pulmonary Health in Cystic Fibrosis; Chapter 15. Mucolytic Therapy and Airway Clearance Techniques; Chapter 16. Pulmonary Exacerbations; Chapter 17. Gastrointestinal Complications of Cystic Fibrosis; Chapter 18. Liver Disease; Chapter 19. Nutrition; Chapter 20. Bone Health and Treatment Chapter 21. Cystic Fibrosis-Related Diabetes and ManagementChapter 22. Other extrapulmonary Complications and Treatment; Chapter 23. Chronic Respiratory Failure and the Roles of Noninvasive Ventilation and Lung Transplantation; Chapter 24. Gene Repair: Past, Present, and Future; Chapter 25. Restoration of CFTR Function with Small-Molecule Modulators; Chapter 26. Quality IMprovement in Cystic Fibrosis Care; Chapter 27. Cystic Fibrosis and Infection Control; Chapter 28. Transition to Adult Care; Chapter 29. Reproduction, Sexuality, and Fertility Chapter 30. A Biopsychosocial Model of Cystic Fibrosis: Social and Emotional Functioning, Adherence, and Quality of LifeChapter 31. Palliative and End-of-Life Care in Cystic Fibrosis; Index; Back Cover |
Record Nr. | UNINA-9910456498103321 |
New York, N.Y. : , : Informa Healthcare USA, , 2010 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
Cystic fibrosis / / edited by Julian L. Allen, Howard B. Panitch, and Ronald C. Rubenstein |
Pubbl/distr/stampa | New York, N.Y. : , : Informa Healthcare USA, , 2010 |
Descrizione fisica | 1 online resource (546 p.) |
Disciplina | 616.3/72 |
Altri autori (Persone) |
AllenJulian Lewis
RubensteinRonald PanitchHoward B |
Collana | Lung biology in health and disease |
Soggetto topico |
Cystic fibrosis
Lungs - Diseases |
ISBN |
0-429-06998-7
1-282-56094-8 9786612560941 1-4398-0182-7 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
Front Cover; Preface; Contents; Chapter 1. The Genetics of Cystic Fibrosis; Chapter 2. Ion Transport; Chapter 3. Mucus Abnormalities and Ciliary Dysfunction; Chapter 4. Microbiology in Cystic Fibrosis; Chapter 5. Inflammation in the Cystic Fibrosis Lung; Chapter 6. Modifier Genes of Cystic Fibrosis; Chapter 7. Cystic Fibrosis: Diagnosis, Sweat Testing, and Newborn Screening; Chapter 8. Diagnostic Approach to Diseases Associated with Cystic Fibrosis Transmembrane Conductance Regulator Gene Mutations; Chapter 9. Lung Function Testing in Infants
Chapter 10. Assessment of Lung Function in Young Children with Cystic FibrosisChapter 11. Lung Function Testing in School-Age Children with Cystic Fibrosis; Chapter 12. Thoracic Imaging in Cystic Fibrosis Pulmonary Disease; Chapter 13. Pulmonary Manifestations; Chapter 14. Treatment Strategies for Maintaining Pulmonary Health in Cystic Fibrosis; Chapter 15. Mucolytic Therapy and Airway Clearance Techniques; Chapter 16. Pulmonary Exacerbations; Chapter 17. Gastrointestinal Complications of Cystic Fibrosis; Chapter 18. Liver Disease; Chapter 19. Nutrition; Chapter 20. Bone Health and Treatment Chapter 21. Cystic Fibrosis-Related Diabetes and ManagementChapter 22. Other extrapulmonary Complications and Treatment; Chapter 23. Chronic Respiratory Failure and the Roles of Noninvasive Ventilation and Lung Transplantation; Chapter 24. Gene Repair: Past, Present, and Future; Chapter 25. Restoration of CFTR Function with Small-Molecule Modulators; Chapter 26. Quality IMprovement in Cystic Fibrosis Care; Chapter 27. Cystic Fibrosis and Infection Control; Chapter 28. Transition to Adult Care; Chapter 29. Reproduction, Sexuality, and Fertility Chapter 30. A Biopsychosocial Model of Cystic Fibrosis: Social and Emotional Functioning, Adherence, and Quality of LifeChapter 31. Palliative and End-of-Life Care in Cystic Fibrosis; Index; Back Cover |
Record Nr. | UNINA-9910781029703321 |
New York, N.Y. : , : Informa Healthcare USA, , 2010 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
Cystic fibrosis / / edited by Julian L. Allen, Howard B. Panitch, Ronald C. Rubenstein |
Edizione | [1st ed.] |
Pubbl/distr/stampa | New York, : Informa Healthcare, c2010 |
Descrizione fisica | 1 online resource (546 p.) |
Disciplina | 616.3/72 |
Altri autori (Persone) |
AllenJulian Lewis
PanitchHoward B RubensteinRonald |
Collana | Lung biology in health and disease |
Soggetto topico |
Cystic fibrosis
Lungs - Diseases |
ISBN |
0-429-06998-7
1-282-56094-8 9786612560941 1-4398-0182-7 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
Front Cover; Preface; Contents; Chapter 1. The Genetics of Cystic Fibrosis; Chapter 2. Ion Transport; Chapter 3. Mucus Abnormalities and Ciliary Dysfunction; Chapter 4. Microbiology in Cystic Fibrosis; Chapter 5. Inflammation in the Cystic Fibrosis Lung; Chapter 6. Modifier Genes of Cystic Fibrosis; Chapter 7. Cystic Fibrosis: Diagnosis, Sweat Testing, and Newborn Screening; Chapter 8. Diagnostic Approach to Diseases Associated with Cystic Fibrosis Transmembrane Conductance Regulator Gene Mutations; Chapter 9. Lung Function Testing in Infants
Chapter 10. Assessment of Lung Function in Young Children with Cystic FibrosisChapter 11. Lung Function Testing in School-Age Children with Cystic Fibrosis; Chapter 12. Thoracic Imaging in Cystic Fibrosis Pulmonary Disease; Chapter 13. Pulmonary Manifestations; Chapter 14. Treatment Strategies for Maintaining Pulmonary Health in Cystic Fibrosis; Chapter 15. Mucolytic Therapy and Airway Clearance Techniques; Chapter 16. Pulmonary Exacerbations; Chapter 17. Gastrointestinal Complications of Cystic Fibrosis; Chapter 18. Liver Disease; Chapter 19. Nutrition; Chapter 20. Bone Health and Treatment Chapter 21. Cystic Fibrosis-Related Diabetes and ManagementChapter 22. Other extrapulmonary Complications and Treatment; Chapter 23. Chronic Respiratory Failure and the Roles of Noninvasive Ventilation and Lung Transplantation; Chapter 24. Gene Repair: Past, Present, and Future; Chapter 25. Restoration of CFTR Function with Small-Molecule Modulators; Chapter 26. Quality IMprovement in Cystic Fibrosis Care; Chapter 27. Cystic Fibrosis and Infection Control; Chapter 28. Transition to Adult Care; Chapter 29. Reproduction, Sexuality, and Fertility Chapter 30. A Biopsychosocial Model of Cystic Fibrosis: Social and Emotional Functioning, Adherence, and Quality of LifeChapter 31. Palliative and End-of-Life Care in Cystic Fibrosis; Index; Back Cover |
Record Nr. | UNINA-9910823422403321 |
New York, : Informa Healthcare, c2010 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|