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000922702 019__ $$a1125931405
000922702 020__ $$a9783030022396$$q(electronic book)
000922702 020__ $$a3030022390$$q(electronic book)
000922702 0247_ $$a10.1007/978-3-030-02239-6$$2doi
000922702 035__ $$aSP(OCoLC)on1120693969
000922702 035__ $$aSP(OCoLC)1120693969$$z(OCoLC)1125931405
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000922702 050_4 $$aRC694.5.I53
000922702 08204 $$a616.13$$223
000922702 24500 $$aAnti-neutrophil cytoplasmic antibody (ANCA) associated vasculitis /$$cRenato Alberto Sinico, Loïc Guillevin, editors.
000922702 260__ $$aCham :$$bSpringer,$$c2020.
000922702 300__ $$a1 online resource (334 pages)
000922702 336__ $$atext$$btxt$$2rdacontent
000922702 337__ $$acomputer$$bc$$2rdamedia
000922702 338__ $$aonline resource$$bcr$$2rdacarrier
000922702 4901_ $$aRare diseases of the immune system
000922702 504__ $$aIncludes bibliographical references and index.
000922702 506__ $$aAccess limited to authorized users.
000922702 520__ $$aThis volume, written by well-known experts in the field, covers all aspects of Anti-Neutrophil Cytoplasmic Antibody (ANCA) Associated Vasculitis (AAV). The expression refers to a group of diseases, characterized by destruction and inflammation of small vessels. The clinical signs vary and affect several organs, such as the kidney, lung, skin, nervous system and others. The opening chapters give some historical hints, explain the genetic basis of the disease and provide insights into the pathogenesis derived from recent experimental studies and guides the reader through classification and nomenclature. A large part of the book is then devoted to a detailed description of the specific related diseases and their clinical presentations, the disease course, and potential complications. The advice regarding treatment is based on the best currently available evidence in this constantly evolving area. The book is part of Springer's series Rare Diseases of the Immune System, which presents recently acquired knowledge on pathogenesis, diagnosis, and therapy with the aim of promoting a more holistic approach to these conditions. AAVs are systemic autoimmune diseases of unknown cause that affect small (to medium) sized blood vessels. They include granulomatosis with polyangiitis (formerly Wegener's granulomatosis), microscopic polyangiitis, and eosinophilic granulomatosis with polyangiitis (formerly Churg-Strauss syndrome). This volume will be an invaluable source of up-to-date information for all practitioners involved in the care of patients with these diseases.
000922702 588__ $$aOnline resource; title from PDF title page (SpringerLink, viewed September 23, 2019).
000922702 650_0 $$aVasculitis.
000922702 7001_ $$aSinico, Renato Alberto.
000922702 7001_ $$aGuillevin, L.$$q(Loïc)
000922702 77608 $$iPrint version:$$aSinico, Renato Alberto.$$tAnti-Neutrophil Cytoplasmic Antibody (ANCA) Associated Vasculitis.$$dCham : Springer, ©2019$$z9783030022389
000922702 830_0 $$aRare diseases of the immune system.
000922702 852__ $$bebk
000922702 85640 $$3SpringerLink$$uhttps://univsouthin.idm.oclc.org/login?url=http://link.springer.com/10.1007/978-3-030-02239-6$$zOnline Access$$91397441.1
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000922702 980__ $$aEBOOK
000922702 980__ $$aBIB
000922702 982__ $$aEbook
000922702 983__ $$aOnline
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