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Edited by Pavel Strnad, Mark L. Brantly and Robert BalsThis Monograph offers a comprehensive and up-to-date overview of AATD. It covers basic biology, genetics, laboratory diagnostics and the major organ manifestations; describes the clinical presentation of AATD in both adults and children; and features chapters on genetic counselling, patient views and future therapies. The content has been tailored to meet the needs of the physician, who takes care of lung and liver patients in daily practice, and the general practitioner, who is responsible for the medical guidance of these patients.Contents list1. Patient view2. Serpinopathies3. Genetics and epidemiology4. Laboratory diagnosis5. Mechanisms of lung disease6. Clinical approach to diagnosis and assessment7. Treatment of lung disease8. Mechanisms of liver disease9. Clinical approach to paediatric liver disease10. Clinical approach to liver disease in adults11. Rare manifestations12. Genetic counselling13. Registries: roles, objectives and registry data study outcomes14. Future directions: diagnostic approaches and therapy with AATThis book also includes clinical casesBibliographic InformationTitle: α1-Antitrypsin DeficiencyEdited by: Pavel Strnad, Mark L. Brantly, Robert BalsPublished: 2019-09-01Copyright year: 2019DOI: 10.1183/2312508X.erm8519ISBN electronic: 978-1-84984-109-2Series: ERS Monograph
