Behçet Syndrome
Editat de Yusuf Yazici, Gulen Hatemi, Emire Seyahi, Hasan Yazicien Limba Engleză Hardback – 14 noi 2019
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Specificații
ISBN-13: 9783030241308
ISBN-10: 3030241300
Pagini: 360
Ilustrații: XVI, 328 p. 98 illus., 75 illus. in color.
Dimensiuni: 178 x 254 mm
Ediția:2nd ed. 2020
Editura: Springer International Publishing
Colecția Springer
Locul publicării:Cham, Switzerland
ISBN-10: 3030241300
Pagini: 360
Ilustrații: XVI, 328 p. 98 illus., 75 illus. in color.
Dimensiuni: 178 x 254 mm
Ediția:2nd ed. 2020
Editura: Springer International Publishing
Colecția Springer
Locul publicării:Cham, Switzerland
Cuprins
Chapter 1. Introduction.- Chapter 2. Disease Definition and Epidemiology.- Chapter 3. Skin Mucosa Involvement and the Pathergy Reaction.- Chapter 4. Eye Disease.- Chapter 5. Nervous System Disease.- Chapter 6. Lung Disease.- Chapter 7. Peripheral Vascular and Cardiac Disease.- Chapter 8. Locomotor System Disease.- Chapter 9. Gastrointestinal Involvement.- Chapter 10. Other Clinical Aspects.- Chapter 11. Pediatric Behçet's Syndrome.- Chapter 12. Histopathology.- Chapter 13. Behçet’s Syndrome and Microbes.- Chapter 14. Thrombophilia in Behçet’s Syndrome.- Chapter 15. Genetics and Epigenetics.- Chapter 16. Disease Mechanisms.- Chapter 17. Prognosis.- Chapter 18. Disease Assessment.- Chapter 19. Management.- Chapter 20. The Patient’s View.- Chapter 21. Future Research Considerations.
Notă biografică
Yusuf Yazici, MD
Clinical Associate Professor of Medicine
New York University School of Medicine
New York, NY, USA
Gulen Hatemi, MD
Professor of Medicine
Istanbul University - Cerrahpaşa
Istanbul, Turkey
Emire Seyahi, MD,
Professor of Medicine
Istanbul University - Cerrahpaşa
Istanbul, Turkey
Hasan Yazici, MD
Professor of Medicine
Academic Hospital
Istanbul, Turkey
Textul de pe ultima copertă
The expanded second edition of this important work provides an up-to-date and comprehensive overview of Behçet syndrome. New and updated chapters focus on recent advances in the areas of pathogenesis, the microbiome, genetics and epigenetics, clustering of symptoms, disease assessment and new treatment options. The book examines how these developments have changed the way physicians approach diagnosis, treatment, and management of Behçet patients. It also analyzes the wide variety of clinical manifestations of the disease including mucocutaneous lesions, intraocular inflammation, central nervous system involvement, deep vein thrombosis and other forms of major vascular disease. Building on the success of its predecessor, the Second Edition of Behçet Syndrome is an invaluable resource for physicians, residents, fellows, and graduate students in rheumatology, dermatology, ophthalmology, neurology, gastroenterology, and internal medicine.
Caracteristici
Examines the latest basic and clinical developments in Behçet syndrome Provides a multidisciplinary approach involving rheumatology, dermatology, ophthalmology, neurology and gastroenterology Reviews recent research in pathogenesis, the microbiome, genetics, and treatment options