Cantitate/Preț
Produs
Total produse
Vezi coșul
Cystic Fibrosis de Julian Allen

Cystic Fibrosis: Lung Biology in Health and Disease

Editat de Julian Allen, Howard Panitch, Ronald Rubenstein
en Limba Engleză Paperback – 31 mai 2017
The median age of survival for those with cystic fibrosis has risen considerably in recent years. This text thoroughly examines the developments and breakthroughs which have led to this improvement in life expectancy. With a focus on the latest discoveries in the diagnosis and treatment of the disease, this book provides a comprehensive overview of the past, current and forthcoming advancements in cystic fibrosis research and clinical care.
Citește tot Restrânge

Toate formatele și edițiile

Toate formatele și edițiile Preț Express
Paperback (1) 47243 lei  43-57 zile
  CRC Press – 31 mai 2017 47243 lei  43-57 zile
Hardback (1) 124439 lei  43-57 zile
  CRC Press – 25 mar 2010 124439 lei  43-57 zile

Din seria Lung Biology in Health and Disease

Preț: 47243 lei

Preț vechi: 57517 lei
-18% Nou

Puncte Express: 709
Preț estimativ în valută:
9042€ • 9424$ • 7527£

Carte tipărită la comandă

Livrare economică 06-20 ianuarie 25

 Adaugă în coș

Wish list
Gift list
Am citit!
Adaugă în listă
Preluare comenzi: 021 569.72.76

Specificații

ISBN-13: 9781138112612
ISBN-10: 1138112615
Pagini: 544
Ilustrații: 100
Dimensiuni: 152 x 229 x 28 mm
Greutate: 0.45 kg
Ediția:1
Editura: CRC Press
Colecția CRC Press
Seria Lung Biology in Health and Disease

Public țintă

Professional Reference

Cuprins

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

Notă biografică

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.

Descriere

The median age of survival for those with cystic fibrosis has risen considerably in recent years. This text thoroughly examines the developments and breakthroughs which have led to this improvement in life expectancy. With a focus on the latest discoveries in the diagnosis and treatment of the disease, this book provides a comprehensive overview of the past, current and forthcoming advancements in cystic fibrosis research and clinical care.