Cystic Fibrosis

Author:   Julian Allen (University of Pennsylvania School of Medicine, The Children’s Hospital of Philadelphia, USA.) ,  Howard Panitch (University of Pennsylvania School of Medicine, The Children’s Hospital of Philadelphia, USA) ,  Ronald Rubenstein (University of Pennsylvania School of Medicine, The Children’s Hospital of Philadelphia, USA)
Publisher:   Taylor & Francis Ltd
ISBN:  

9781138112612


Pages:   544
Publication Date:   31 May 2017
Format:   Paperback
Availability:   In Print   Availability explained
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Cystic Fibrosis


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Author:   Julian Allen (University of Pennsylvania School of Medicine, The Children’s Hospital of Philadelphia, USA.) ,  Howard Panitch (University of Pennsylvania School of Medicine, The Children’s Hospital of Philadelphia, USA) ,  Ronald Rubenstein (University of Pennsylvania School of Medicine, The Children’s Hospital of Philadelphia, USA)
Publisher:   Taylor & Francis Ltd
Imprint:   CRC Press
Weight:   1.010kg
ISBN:  

9781138112612


ISBN 10:   1138112615
Pages:   544
Publication Date:   31 May 2017
Audience:   Professional and scholarly ,  Professional & Vocational
Format:   Paperback
Publisher's Status:   Active
Availability:   In Print   Availability explained
This item will be ordered in for you from one of our suppliers. Upon receipt, we will promptly dispatch it out to you. For in store availability, please contact us.

Table of Contents

Preface; Pathophysiology; The Genetics of Cystic Fibrosis; Ion Transport; Mucus Abnormalities and Ciliary Dysfunction; Microbiology in Cystic Fibrosis; Inflammation in the Cystic Fibrosis Lung; Modifier Genes of Cystic Fibrosis; Diagnostics; Cystic Fibrosis: Diagnosis, Sweat Testing, and Newborn Screening; Diagnostic Approach to Diseases Associated with Cystic Fibrosis Transmembrane Conductance Regulator Gene Mutations; Lung Function Testing in Infants; Assessment of Lung Function in Young Children with Cystic Fibrosis; Lung Function Testing in School-Age Children with Cystic Fibrosis; Thoracic Imaging in Cystic Fibrosis Pulmonary Disease; Clinical Manifestations and Treatment; Pulmonary Manifestations; Treatment Strategies for Maintaining Pulmonary Health in Cystic Fibrosis; Mucolytic Therapy and Airway Clearance Techniques; Pulmonary Exacerbations; Gastrointestinal Complications of Cystic Fibrosis; Liver Disease; Nutrition; Bone Health and Treatment; Cystic Fibrosis-Related Diabetes and Management; Other Extrapulmonary Complications and Treatment; Chronic Respiratory Failure and the Roles of Noninvasive Ventilation and Lung Transplantation; Gene Repair: Past, Present, and Future; Restoration of CFTR Function with Small-Molecule Modulators; Psychosocial Considerations and Care Systems; Quality Improvement in Cystic Fibrosis Care; Cystic Fibrosis and Infection Control; Transition to Adult Care; Reproduction, Sexuality, and Fertility; A Biopsychosocial Model of Cystic Fibrosis: Social and Emotional Functioning, Adherence, and Quality of Life; Palliative and End-of-Life Care in Cystic Fibrosis

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Author Information

Julian L. Allen, Howard B. Panitch, Ronald C. Rubenstein, all from the University of Pennsylvania School of Medicine, The Children’s Hospital of Philadelphia, Philadelphia, Pennsylvania, U.S.A.

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