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Cystic fibrosis / / edited by Julian L. Allen, Howard B. Panitch, and Ronald C. Rubenstein
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
Opac: Controlla la disponibilità qui
Cystic fibrosis / / edited by Julian L. Allen, Howard B. Panitch, and Ronald C. Rubenstein
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
Opac: Controlla la disponibilità qui
Cystic fibrosis / / edited by Julian L. Allen, Howard B. Panitch, Ronald C. Rubenstein
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
Opac: Controlla la disponibilità qui