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Antiphospholipid antibody syndromefr...

Meroni, Pier Luigi.

Antiphospholipid antibody syndromefrom bench to bedside /

Record Type:	Electronic resources : Monograph/item
Title/Author:	Antiphospholipid antibody syndromeedited by Pier Luigi Meroni.
Reminder of title:	from bench to bedside /
other author:	Meroni, Pier Luigi.
Published:	Cham :Springer International Publishing :2015.
Description:	x, 267 p. :ill., digital ;24 cm.
Contained By:	Springer eBooks
Subject:	Antiphospholipid syndrome.
Online resource:	http://dx.doi.org/10.1007/978-3-319-11044-8
ISBN:	9783319110448 (electronic bk.)

Antiphospholipid antibody syndromefrom bench to bedside /
Antiphospholipid antibody syndromefrom bench to bedside /[electronic resource] :edited by Pier Luigi Meroni. - Cham :Springer International Publishing :2015. - x, 267 p. :ill., digital ;24 cm. - Rare diseases of the immune system,2282-6505. - Rare diseases of the immune system..

Foreword -- Preface -- 1 APS: Introductory notes -- 2 Immunology and Genetics of APS -- 3 The paradox of the lupus anticoagulant -- 4 The pathogenic mechanism(s) for APS-mediated thrombosis -- 5 The pathogenic mechanism(s) for APS-mediated pregnancy loss -- 6 Classification criteria -- 7 Non-classification criteria -- 8 Obstetric APS -- 9 APS and the nervous system -- 10 APS and renal involvement -- 11 Non-thrombotic hematologic manifestations in APS -- 12 Heart and APS -- 13 Skin and APS -- 14 Additional organs involved in APS (eye, ENT, GI, endocrine) -- 15 Treatment of thrombosis -- 16 Treatment of pregnancy complications -- 17 Asymptomatic carries of APS -- 18 New treatments -- 19 Secondary APS -- 20 Catastrophic APS.

This book, part of the series Rare Diseases of the Immune System, offers comprehensive, up-to-date coverage of the pathophysiology and management of the antiphospholipid syndrome (APS). Immunologic and genetic aspects are discussed and the pathogenic mechanisms responsible for such phenomena as APS-mediated thrombosis and pregnancy loss or complications are explained. The main clinical manifestations and classification criteria are described and diagnostic tools, identified. Close attention is paid to the nature of the involvement of other organs or organ systems in APS, including the nervous, endocrine, hematologic, cardiovascular, and gastrointestinal systems, the kidney, the skin, and the eye. Specific chapters describe the treatment of the different symptoms, the preventive therapies of value in avoiding recurrences, and innovative treatment approaches. The authors are senior experts in the field who are aided by younger fellows, ensuring that the book is also educationally oriented. This handy volume will be a valuable tool for postgraduates in training and professionals wishing to extend their knowledge of this specific syndrome

ISBN: 9783319110448 (electronic bk.)

Standard No.: 10.1007/978-3-319-11044-8doiSubjects--Topical Terms:

454047
Antiphospholipid syndrome.

LC Class. No.: RC600

Dewey Class. No.: 616.978

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505 0 $a Foreword -- Preface -- 1 APS: Introductory notes -- 2 Immunology and Genetics of APS -- 3 The paradox of the lupus anticoagulant -- 4 The pathogenic mechanism(s) for APS-mediated thrombosis -- 5 The pathogenic mechanism(s) for APS-mediated pregnancy loss -- 6 Classification criteria -- 7 Non-classification criteria -- 8 Obstetric APS -- 9 APS and the nervous system -- 10 APS and renal involvement -- 11 Non-thrombotic hematologic manifestations in APS -- 12 Heart and APS -- 13 Skin and APS -- 14 Additional organs involved in APS (eye, ENT, GI, endocrine) -- 15 Treatment of thrombosis -- 16 Treatment of pregnancy complications -- 17 Asymptomatic carries of APS -- 18 New treatments -- 19 Secondary APS -- 20 Catastrophic APS.
520 $a This book, part of the series Rare Diseases of the Immune System, offers comprehensive, up-to-date coverage of the pathophysiology and management of the antiphospholipid syndrome (APS). Immunologic and genetic aspects are discussed and the pathogenic mechanisms responsible for such phenomena as APS-mediated thrombosis and pregnancy loss or complications are explained. The main clinical manifestations and classification criteria are described and diagnostic tools, identified. Close attention is paid to the nature of the involvement of other organs or organ systems in APS, including the nervous, endocrine, hematologic, cardiovascular, and gastrointestinal systems, the kidney, the skin, and the eye. Specific chapters describe the treatment of the different symptoms, the preventive therapies of value in avoiding recurrences, and innovative treatment approaches. The authors are senior experts in the field who are aided by younger fellows, ensuring that the book is also educationally oriented. This handy volume will be a valuable tool for postgraduates in training and professionals wishing to extend their knowledge of this specific syndrome
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