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020			_a9783030022396
024	7		_a10.1007/978-3-030-02239-6 _2doi
040			_aES-MaUEC _bspa _cES-MaUEC _dES-MaUEC
050		4	_aRC694.5 _b.A58 2020 EB
245	0	0	_aAnti-Neutrophil Cytoplasmic Antibody (ANCA) Associated Vasculitis _cedited by Renato Alberto Sinico, Loïc Guillevin.
250			_a1st ed. 2020.
264		1	_aCham _bSpringer International Publishing : _bImprint: Springer _c2020.
300			_a1 recurso en línea (X, 336 páginas) _b52 ilustraciones, 35 ilustraciones a color
336			_2rdacontent _aTexto _btxt
337			_2rdamedia _aelectrónico _bc
338			_2rdacarrier _arecurso electrónico _bcr
347			_atext file _bPDF
490	0		_aRare Diseases of the Immune System _x2282-6505
490	0		_aMedicine (Springer-11650)
505	0		_aPreface -- 1 Introduction: Nomenclature and Classification -- 2 Epidemiology -- 3 Genetics -- 4 Pathogenesis B lymphocytes T lymphocytes -- 5 ANCA: methods and clinical significance -- 6 Activity and Damage -- 7 Eosinophilic Granulomatosis with Polyangiitis (EGPA) -- 8 Granulomatosis with Polyangiitis (GPA) -- 9 Microscopic Polyangiitis (MPA) -- 10 Vasculitis /organs involvement -- 11 ENT involvement -- 12 Lung involvement -- 13 Kidney involvement -- 14 Nervous system involvement. 15 Peripheral Nervous System -- 16 Central Nervous System -- 17 Skin involvement -- 18 Miscellaneous organ/system involvement (heart, gastrointestinal, articular....) -- 19 Prognosis and outcome -- 20 Therapy -- Subject Index.
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.
988			_aSegundosemestre_2019_Medicine
650		0	_2embne _9541194 _aVasculitis
700	1		_aSinico, Renato Alberto _eeditor _4edt _4http://id.loc.gov/vocabulary/relators/edt
700	1		_aGuillevin, Loïc _eeditor _4edt _4http://id.loc.gov/vocabulary/relators/edt
710	2		_aSpringerLink (Online service) _9106937
773	0		_tSpringer eBooks
776	0	8	_iPrinted edition: _z9783030022389
776	0	8	_iPrinted edition: _z9783030022402
856	4	0	_uhttps://go.openathens.net/redirector/universidadeuropea.es?url=https://doi.org/10.1007/978-3-030-02239-6 _zAcceso a este recurso digital (usuarios Universidad Europea de Valencia)
942			_2lcc _cLE
998			_db _feng _ggw _h0 _ea _zSI