Behçet's Disease: A Guide to its Clinical Understanding Textbook and Atlas
A Turkish dermatologist named Hulusi Beh~et defined a syndrome, the major symptoms of which comprise oral ulcers, genital ulcers, eye lesions, and skin lesions, as a specific disease in 1937, and the disease was named Beh~et's disease after him. Since then, there have been more than 4500 reports presented world­ wide on this disease showing that Beh~et's disease is no longer rare. Because Beh~et's disease is clinically dynamic and its clinical symptoms are various and their spectrum very wide. However, there are insufficient pathognomic laborato­ ry data for the diagnosis of Beh~et's disease, so it is with great difficulty that Beh~et's disease specialists diagnose the disease based only on their clinical expe­ rience. We have therefore collected data from more than 5500 living Beh~et's disease patients whom we have seen, and we have brought together data from other nations and other continents. We hope the result is a clinical guide for those inter­ ested in Beh~et's disease. To improve the accessibility of the information, this text­ book was made in a photo-monography style with an atlas style, and we have tried our best to make our sentences short and clear. We are grateful to the many scholars worldwide whose contributions have added greatly to the value of this textbook. We are especially grateful to the staff of Springer-Verlag who have shown deep kindness and patience. Special thanks to Ms. Heather Yu for helping us in writing this monograph in English, and Mr. Jung-Woon Lee for his assistance.
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Behçet's Disease: A Guide to its Clinical Understanding Textbook and Atlas
A Turkish dermatologist named Hulusi Beh~et defined a syndrome, the major symptoms of which comprise oral ulcers, genital ulcers, eye lesions, and skin lesions, as a specific disease in 1937, and the disease was named Beh~et's disease after him. Since then, there have been more than 4500 reports presented world­ wide on this disease showing that Beh~et's disease is no longer rare. Because Beh~et's disease is clinically dynamic and its clinical symptoms are various and their spectrum very wide. However, there are insufficient pathognomic laborato­ ry data for the diagnosis of Beh~et's disease, so it is with great difficulty that Beh~et's disease specialists diagnose the disease based only on their clinical expe­ rience. We have therefore collected data from more than 5500 living Beh~et's disease patients whom we have seen, and we have brought together data from other nations and other continents. We hope the result is a clinical guide for those inter­ ested in Beh~et's disease. To improve the accessibility of the information, this text­ book was made in a photo-monography style with an atlas style, and we have tried our best to make our sentences short and clear. We are grateful to the many scholars worldwide whose contributions have added greatly to the value of this textbook. We are especially grateful to the staff of Springer-Verlag who have shown deep kindness and patience. Special thanks to Ms. Heather Yu for helping us in writing this monograph in English, and Mr. Jung-Woon Lee for his assistance.
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Behçet's Disease: A Guide to its Clinical Understanding Textbook and Atlas

Behçet's Disease: A Guide to its Clinical Understanding Textbook and Atlas

Behçet's Disease: A Guide to its Clinical Understanding Textbook and Atlas

Behçet's Disease: A Guide to its Clinical Understanding Textbook and Atlas

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Overview

A Turkish dermatologist named Hulusi Beh~et defined a syndrome, the major symptoms of which comprise oral ulcers, genital ulcers, eye lesions, and skin lesions, as a specific disease in 1937, and the disease was named Beh~et's disease after him. Since then, there have been more than 4500 reports presented world­ wide on this disease showing that Beh~et's disease is no longer rare. Because Beh~et's disease is clinically dynamic and its clinical symptoms are various and their spectrum very wide. However, there are insufficient pathognomic laborato­ ry data for the diagnosis of Beh~et's disease, so it is with great difficulty that Beh~et's disease specialists diagnose the disease based only on their clinical expe­ rience. We have therefore collected data from more than 5500 living Beh~et's disease patients whom we have seen, and we have brought together data from other nations and other continents. We hope the result is a clinical guide for those inter­ ested in Beh~et's disease. To improve the accessibility of the information, this text­ book was made in a photo-monography style with an atlas style, and we have tried our best to make our sentences short and clear. We are grateful to the many scholars worldwide whose contributions have added greatly to the value of this textbook. We are especially grateful to the staff of Springer-Verlag who have shown deep kindness and patience. Special thanks to Ms. Heather Yu for helping us in writing this monograph in English, and Mr. Jung-Woon Lee for his assistance.

Product Details

ISBN-13: 9783642564550
Publisher: Springer-Verlag New York, LLC
Publication date: 12/06/2012
Sold by: Barnes & Noble
Format: eBook
File size: 23 MB
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Table of Contents

I Special Contribution.- Advances in the Immunopathogenesis of Behçet’s Disease.- II Clinical Understanding of Behçet’s Disease.- 1 Introduction.- 2 Etiopathogenesis.- 3 Clinical Manifestations.- 4 Diagnosis.- 5 Immunologic Aspects.- 6 Histopathology.- 7 Interdepartmental Cooperation Approach System.- 8 Therapy.- 9 Prognosis.- 10 Prevention.- 11 Animal Models.- Appendix Special issue on Behçet’s Disease of Yonsei Medical Journal (Vol 38, No. 6, December 1997).- Appendix 1 Life Story of Dr. Hûlusi Behçet.- Appendix 2 Molecular Genetics (HLA) of Behçet’s Disease.- Appendix 3 Behçet’s Disease Etiopathology: Immunological Aspects*.- Appendix 4 Etiopathology of Behçet’s Disease: Herpes Simplex Virus Infection and Animal Model.- Appendix 5 Diagnostic Criteria of Behçet’s Diesease: Problems and Suggestions.- Appendix 6 Recurrent Aphthous Stomatitis in the Diagnosis of Behçet’s Disease*.- Appendix 7 Dermatologic Manifestation of Behçet’s Disease.- Appendix 8 Ophthalmologic Manifestations of Behçet’s Disease.- Appendix 9 Behçet’s Disease — A Rheumatologic Perspective.- Appendix 10 Treatment of Behçet’s Disease.- Appendix 11 Adamantiades-Behçet’s Disease: Epidemiology in Germany and in Europe*.- Appendix 12 Clinical Manifestations of Behçet’s Disease: An Analysis of 2147 Patients*.- Appendix 13 Epidemiological and Clinical Features of Behçet’s Disease in Korea.- Appendix 14 The Influence of Pregnancy on Behçet’s Disease.- Appendix 15 Immunological Aspects of Hyperreactivity to Streptococcal Antigens in Behçet’s Disease*.- Appendix 16 Surgical Treatment of Intestinal Behçet’s Disease.
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