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Cystic Fibrosis
Cystic fibrosis (CF) is one of the most common fatal hereditary diseases. The discovery of the cystic fibrosis transmembrane conductance regulator (CFTR) gene 25 years ago set the stage for unraveling the pathogenesis of CF lung disease, continuous refinement of symptomatic treatments and the development of mutation-specific therapies, which are now becoming available for a subgroup of patients. This ERS Monograph provides an update on all aspects of CF lung disease, from infancy to adulthood, including current concepts on disease process, improvements in early diagnosis and monitoring, therapeutic approaches, and patient care. The book highlights important recent developments and discusses the next steps that will be required for further improvement of the life expectancy and quality of life of CF patients. It will be an essential reference for basic and clinical scientists and all members of the CF team.
Bronchiectasis, An Issue of Clinics in Chest Medicine
The first issue of Clinics in Chest Medicine to be published with this focus, this issue reviews bronchiectasis from numerous angles to provide comprehensive coverage on this important subject. Epidemiology, airway defense mechanisms, pathogenesis, imaging and genetic causes of bronchiectasis are discussed. Allergic bronchopulmonary aspergillosis is addressed, as well as non-tuberculous mycobacteria as a cause of bronchiectasis. Authors examine how to evaluate the success of therapy for bronchiectasis (what endpoints to use) and then discuss a variety of therapy options: inhaled and systemic antibiotic treatment, chest physiotherapy, pharmacologic agents for mucous clearance, antipinflammatory therapy and macrolides. Pulmonary resection and lung transplantation for bronchiectasis are reviewed. Recent advances in Cystic Fibrosis are also discussed.
Philosophy for Public Health and Public Policy
This work argues that philosophy is not just useful, but vital, for thinking coherently about priorities in health policy and public policy.
The Spectrum of Bronchial Infection
Lower respiratory tract infections are one the most frequent causes of medical consultation in primary care. They are also one of the main causes of emergency visits and hospital admissions. The majority of these infections occur in the bronchial tree and include a large spectrum of aetiologies and clinical manifestations, from mild acute bronchitis to severe bronchiectasis and exacerbations of chronic obstructive pulmonary disease. In this Monograph, a series of prestigious researchers and clinicians provide an overview of the advances in the pathogenesis, manifestations and new approaches to treatment of bronchial infection in a wide variety of clinical scenarios. This book offers the reader the best existing scientific evidence that can be applied to the care of patients with any kind of bronchial infection.
Sessional Papers
"Report of the Dominion fishery commission on the fisheries of the province of Ontario, 1893", issued as vol. 26, no. 7, supplement.
Hodson and Geddes' Cystic Fibrosis
Hodson and Geddes' Cystic Fibrosis provides everything the respiratory clinician, pulmonologist or health professional treating patients needs in a single manageable volume. This international and authoritative work brings together current knowledge and has become established in previous editions as a leading reference in the field. This fourth edition includes a wealth of new information, figures, useful videos, and a companion eBook. The basic science that underlies the disease and its progression is outlined in detail and put into a clinical context. Diagnostic and clinical aspects are covered in depth, as well as promising advances such as gene therapies and other novel molecular based t...
Chemistry and Biology of Serpins
Proceedings of an International Symposium held in Chapel Hill, North Carolina, April 13-16, 1996
