دانلود کتاب فیبروز کیستیک هادسون و گدس
Hodson and Geddes’ Cystic Fibrosis, 4ed

Review

About the Author

Contents

Chapter 1: Introduction: From the discovery of the CFTR gene in 1989 through to 2014
Chapter 2: Epidemiology of cystic fibrosis
Chapter 3: Living with cystic fibrosis: The voices of patients and families
Chapter 4: Molecular biology of cystic fibrosis: CFTR processing and functions and classes of mutations
Chapter 5: Underlying concepts of the pathophysiology of cystic fibrosis in the sweat glandr GI tract, and lung
Chapter 6: What have we learned from animal models?
Chapter 7: Interactions between infection and inflammation in the cystic fibrosis airway
Chapter 8: CFTR and interactions with modifier genes and the environment: Genotype-phenotypecorrelations and modifier genes
Chapter 9: CFTR and interactions with modifier genes and the environment: Environment
Chapter 10: Diagnosis of the symptomatic patient
Chapter 11: Screening: What tests?
Chapter 12: Pathway of pain: Your normal baby has a life-threatening disease
Chapter 13: Microbiology of cystic fibrosis: Epidemiology of cystic fibrosis pathogens and clinical microbiology laboratory methods
Chapter 14: New methods for detecting and identifying bacteria
Chapter 15: Infection control
Chapter 16: Respiratory disease: Infectious complications
Chapter 17: Pulmonary exacerbations
Chapter 18: Respiratory disease: Noninfectious complications
Chapter 19: Sleep, lung mechanics,and work of breathing, including noninvasive ventilation
Chapter 20: Delivering therapy to the cystic fibrosis lung
Chapter 21: Upper airway disease
Chapter 22: Gastrointestinal disease in cystic fibrosis
Chapter 23: The liver in cystic fibrosis
Chapter 24: Insulin deficiency and cystic fibrosis-related diabetes
Chapter 25: Growth and puberty
Chapter 26: Bone disease
Chapter 27: Other cystic fibrosis-related disease
Chapter 28: Sexual and reproductive issues
Chapter 29: Transplantation
Chapter 30: Growing old with cystic fibrosis
Chapter 31: Quality improvement: Using databases to improve cystic fibrosis care
Chapter 32: Infant and preschool lung function
Chapter 33: Role of bronchoscopy and bronchoalveolar lavage in infants with cystic fibre
Chapter 34: Clinical and radiological aspects of imaging the lungs
Chapter 35: Physiological monitoring of older children and adults
Chapter 36: Exercise: Testing and use in therapy
Chapter 37: Outcome of clinical trials: Electricity, induced sputum, and breath
Chapter 38: Chest computed tomography and clinical trials in cystic fibrosis
Chapter 39: Outcomes of clinical trials: Multiple breath washout tests in cystic fibrosis
Chapter 40: What have we learned over the last 5 years?
Chapter 41: Cystic fibrosis center care
Chapter 42: Nursing
Chapter 43: Physiotherapy
Chapter 44: Nutritional aspects
Chapter 45: Psychology
Chapter 46: Palliative and spiritual care
Chapter 47: Basic science: What will it deliver? Gene and stem cell therapy
Chapter 48: Basic science: What will it deliver? Non-genetherapy treatments
Chapter 49: The future: Flow will management change?