000			03457nam a22003735i 4500
001			82215
003			ES-MaUEC
005			20230207040401.0
007			cr nn 008mamaa
008			141120s2015 gw | s |||| 0|eng d
020			_a9783319110448
024	7		_a10.1007/978-3-319-11044-8 _2doi
050		4	_aRC600 _b2015 EB
245	1	0	_aAntiphospholipid Antibody Syndrome : _bFrom Bench to Bedside _cedited by Pier Luigi Meroni.
260			_aCham, Switzerland _bSpringer _c2015
300			_a1 recurso en línea (X, 267 páginas) _b19 ilustraciones, 15 ilustraciones en color
336			_aTexto _btxt _2rdacontent
337			_aelectrónico _bc _2rdamedia
338			_arecurso electrónico _bcr _2rdacarrier
490	0		_aRare Diseases of the Immune System _x2282-6505
505	0		_aForeword -- 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 -- 20Â{u2820} Catastrophic APS.
520	3		_aThis 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.
710	2		_aSpringerLink (Online service) _0Local _9106996
942			_2lcc _cLE
650		7	_aReumatología _0 _2embne _9141883
650	2	7	_aReumatología _0 _2embne _9141883
650		7	_aGinecología _0 _2embne _9138562
700	1		_aMeroni, Pier Luigi _eeditor literario _994990 _0Local
856	4	0	_uhttps://go.openathens.net/redirector/universidadeuropea.es?url=https://link.springer.com/book/10.1007/978-3-319-11044-8 _zAcceso a este recurso digital (usuarios Universidad Europea de Madrid)
907			_a.b12908551 _b10-10-17 _c10-02-16
988			_aSpringer_Medicine_2015
998			_am _a_alco _a_vill _b - - _cm _dz _e- _feng _ggw _h0
945			_aRC600 .A585 2015 EB _g1 _ieBOOK _j0 _lmae _o- _pEUR0.00 _q- _r- _sb _t15 _u0 _v0 _w0 _x0 _y.i11576236 _z06-04-17
999			_c82215 _d82215 _x1