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Antiphospholipid syndrome in systemi...
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Cervera, Ricard.
Antiphospholipid syndrome in systemic autoimmune diseases
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Antiphospholipid syndrome in systemic autoimmune diseaseseditors, R. Cervera, Munther A. Khamashta, Joan Carles Reverter.
其他作者:
Reverter, Joan Carles.
出版者:
Amsterdam ;Elsevier Science,2009.
面頁冊數:
p.cm.
標題:
Antiphospholipid syndrome.
電子資源:
An electronic book accessible through the World Wide Web; click for information
ISBN:
9780444531698
Antiphospholipid syndrome in systemic autoimmune diseases
Antiphospholipid syndrome in systemic autoimmune diseases
[electronic resource] /editors, R. Cervera, Munther A. Khamashta, Joan Carles Reverter. - Amsterdam ;Elsevier Science,2009. - p.cm. - Handbook of systemic autoimmune diseases ;10. - Handbook of systemic autoimmune diseases ;10..
Classification and Epidemiology of the Antiphospholipid Syndrome -- Laboratory Heterogeneity of the Antiphospholipid Antibodies -- Pathogenesis of the Antiphospholipid Syndrome -- Immunogenetics of the Antiphospholipid Syndrome -- Systemic Manifestations of the Antiphospholipid Syndrome -- Obstetric Manifestations of the Antiphospholipid Syndrome -- Antiphospholipid Antibodies and Infections and Drugs -- Antiphospholipid Antibodies and Malignancies -- Antiphospholipid Antibodies and Vascular Disorders (Atheromatosis and Vasculitis) -- Treatment of the Antiphospholipid Syndrome -- Difficult situations in the Antiphospholipid Syndrome.
Antiphospholipid syndrome is an autoimmune disease which causes abnormal blood clots. It is now recognised as a major cause of common conditions, including stroke, heart attack, miscarriage, epilepsy and memory loss and as such is gaining recognition in all branches of medicine, from obstetrics to cardiology, from psychiatry to orthopaedics.<BR id="CRLF"><BR id="CRLF">This book provides an overview of our current understanding of this major disease. It includes the latest information on the new pathogenetic mechanisms involved as well as clinical manifestations in both b3 sthe thrombotic b4 s and b3 snon thrombotic b4 s manifestations of this important disease. * Comprehensive review of this major disease<BR id="CRLF">* Includes information on treatment options available.
Electronic reproduction.
Amsterdam :
Elsevier Science & Technology,
2009.
Mode of access: World Wide Web.
ISBN: 9780444531698
Source: 140964:141106Elsevier Science & Technologyhttp://www.sciencedirect.comSubjects--Topical Terms:
454047
Antiphospholipid syndrome.
Index Terms--Genre/Form:
214472
Electronic books.
LC Class. No.: RC600 / .A58 2009
Dewey Class. No.: 616.978
Antiphospholipid syndrome in systemic autoimmune diseases
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Classification and Epidemiology of the Antiphospholipid Syndrome -- Laboratory Heterogeneity of the Antiphospholipid Antibodies -- Pathogenesis of the Antiphospholipid Syndrome -- Immunogenetics of the Antiphospholipid Syndrome -- Systemic Manifestations of the Antiphospholipid Syndrome -- Obstetric Manifestations of the Antiphospholipid Syndrome -- Antiphospholipid Antibodies and Infections and Drugs -- Antiphospholipid Antibodies and Malignancies -- Antiphospholipid Antibodies and Vascular Disorders (Atheromatosis and Vasculitis) -- Treatment of the Antiphospholipid Syndrome -- Difficult situations in the Antiphospholipid Syndrome.
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Antiphospholipid syndrome is an autoimmune disease which causes abnormal blood clots. It is now recognised as a major cause of common conditions, including stroke, heart attack, miscarriage, epilepsy and memory loss and as such is gaining recognition in all branches of medicine, from obstetrics to cardiology, from psychiatry to orthopaedics.<BR id="CRLF"><BR id="CRLF">This book provides an overview of our current understanding of this major disease. It includes the latest information on the new pathogenetic mechanisms involved as well as clinical manifestations in both b3 sthe thrombotic b4 s and b3 snon thrombotic b4 s manifestations of this important disease. * Comprehensive review of this major disease<BR id="CRLF">* Includes information on treatment options available.
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