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020 _a9784431544876
040 _aES-MaUEC
050 4 _aRC122.B4
_b2015 EB
082 0 4 _a616.723
245 0 0 _aBehçet's disease :
_bfrom genetics to therapies
_cedited by Yoshiaki Ishigatsubo
260 _aTokyo
_bSpringer
_ccop. 2015
300 _a1 recurso en línea (IX, 176 p.)
_bil.
336 _aTexto (visual)
_btxt
_2rdacontent
337 _aelectrónico
_bc
_2rdamedia
338 _arecurso electrónico
_bcr
_2rdacarrier
338 _aonline resource
_bcr
_2rdacarrier
347 _atext file
_bPDF
_2rda
520 _aThis book, besides reviewing basic and clinical aspects of BehÃ{u00A7}et's disease, covers the latest findings, including genetic studies and treatment with biologics for the disease. Although the cause of BehÃ{u00A7}et's disease is still unknown, it is well known that genetic factors, such as HLA-B51, are involved in its development. Recently, novel susceptibility loci including IL10, IL23R-IL12RB2, and endoplasmic reticulum aminopeptidase 1 have been identified, providing new insights into the pathogenesis of the disease. In addition to basic research, the beneficial efficacy of anti-TNF-alpha monoclonal antibodies has also been suggested for not only uveitis associated with the disease but also other subtypes of the disease such as entero-, vasculo-, and neuro- BehÃ{u00A7}et's disease. BehÃ{u00A7}et's Disease:Â{u01B2}om Genetics to Therapies Â{u0CAF}vides essential information both for basic researchers working in the fields of immunology, inflammation, and genetics, and for clinical physicians who are interested in BehÃ{u00A7}et's disease, such as ophthalmologists, rheumatologists, dermatologists, gastroenterologists, neurologists, and vascular surgeons.
650 0 7 _aSíndrome de Behçet
_0LocalX
_2embne
_9672746
700 1 _aIshigatsubo, Yoshiaki
_eeditor literario
_995641
_0Local
856 4 0 _uhttps://go.openathens.net/redirector/universidadeuropea.es?url=https://link.springer.com/book/10.1007/978-4-431-54487-6
_zAcceso a este recurso digital (usuarios Universidad Europea de Madrid)
901 _ai9784431544876
907 _a.b12912414
_b10-10-17
_c10-02-16
942 _2lcc
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945 _aRC122.B4 B44 2015 EB
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