000 04456cam a2200421Ii 4500
001 95682
003 ES-MaUEC
005 20230102112716.0
006 m o d
007 cr cnu---unuuu
008 170330s2017 sz a o 000 0 eng d
020 _a3319525425
_q(electronic bk.)
020 _a9783319525426
_q(electronic bk.)
020 _z3319525417
020 _z9783319525419
_q(print)
040 _aGW5XE
_cGW5XE
_dGW5XE
_dN$T
_dEBLCP
_dYDX
_dUAB
_dNJR
_dUPM
_dOCLCF
_dIOG
_dCOO
_dESU
_dJBG
_dIAD
_dICW
_dICN
_dOTZ
_dVT2
_dJG0
_dU3W
_dES-MaUEC
_bspa
050 4 _aRC582
_b.I347 2017 EB
245 0 0 _aIgG4-related disease
_cKazuichi Okazaki, editor.
246 3 _aImmunoglobulin G4-related disease
264 1 _aCham, Switzerland
_bSpringer
_c[2017]
300 _a1 recurso en línea (vii, 128 páginas)
_bilustraciones
336 _aTexto
_btxt
_2rdacontent
337 _aelectrónico
_bc
_2rdamedia
338 _arecurso electrónico
_bcr
_2rdacarrier
347 _atext file
_bPDF
_2rda
490 0 _aCurrent topics in microbiology and immunology
_vvolume 401
500 _aSpringerLink
_bSpringer Biomedical and Life Sciences eBooks 2017 English+International
505 0 _aPreface; Contents; 47 Current Concept of IgG4-Related Disease; Abstract; 1 The History of IgG4-Related Disease: Before and After Discovery of IgG4 (Table 1); 2 Current Concepts of IgG4-RD; 3 Nomenclatures and Individual Organ Manifestation of IgG4-RD; 3.1 Type 1 Autoimmune Pancreatitis (IgG4-Related Pancreatitis); 3.2 IgG4-Related Sclerosing Cholangitis (IgG4-SC); 3.3 IgG4-Related Dacryoadenitis and Sialoadenitis (Formerly Called Mikulicz's Disease); 3.4 IgG4-Related Ophthalmic Diseases (IgG4-Related OD); 3.5 IgG4-Related Kidney Disease (IgG4-Related KD)
505 8 _a3.2 Small-Scale GWAS for Detecting Genetic Factors Causing the Development of Lachrymal/Salivary Gland Lesions in AIP4 Conclusions and Future Perspectives; References; 38 The Histopathology of IgG4-Related Disease; Abstract; 1 Diagnosis of IgG4-Related Disease; 2 General Pathological Features of IgG4-RD; 2.1 Morphological Features; 2.2 Immunohistochemical Features; 3 Proposed Diagnostic Terminology for IgG4-RD; 4 Pancreatobiliary Manifestations; 5 Sialadenitis and Dacryoadenitis; 6 Lung Disease; 7 Periaortitis, Inflammatory Aneurysm, and Retroperitoneal Fibrosis; 8 Lymphadenopathy; 9 Summary
505 8 _a3.4 Treatment-Related Side Effects4 Prognosis; 5 Future Perspectives; References; 37 Immunogenetics of IgG4-Related AIP; Abstract; 1 Introduction; 2 Association Studies Using Polymorphic Markers in Candidate Genes; 2.1 Human Leukocyte Antigen (HLA) Complex; 2.2 Fc Receptor-Like 3 (FCRL3) Gene; 2.3 Cytotoxic T-Lymphocyte Antigen-4 (CTLA-4; CD152) Gene; 2.4 Toll-Like Receptor 4 (TLR4) and Protein Tyrosine Phosphatase N22 (PTPN22) Genes; 3 Association Studies Using Genome-Wide Polymorphic Markers; 3.1 Microsatellite Markers
505 8 _a3.6 IgG4-Related Retroperitoneal Fibrosis (IgG4-Related RPF)3.7 IgG4-Related Pulmonary Diseases (IgG4-Related PD); 3.8 IgG4-Related Thyroid Disease; 3.9 IgG4-Related Aortitis/Periaortitis; 3.10 IgG4-Related Lymphadenopathy; Acknowledgment; References; 36 Diagnosis and Treatment of IgG4-Related Disease; Abstract; 1 Introduction; 2 Diagnosis; 2.1 Epidemiology; 2.2 Clinical Symptoms; 2.3 Laboratory Tests; 2.4 Imaging; 2.5 Histopathology; 2.6 Steroid Responsiveness; 2.7 Diagnostic Criteria; 3 Treatment; 3.1 Indication of Treatment; 3.2 Induction of Remission; 3.3 Relapse and Maintenance Therapy
520 3 _aThis volume focuses on IgG4-related disease (IgG4-RD), a novel clinical entity involving multiple organs and of unknown origin, associated with the abundant infiltration of IgG4-positive cells. It consists of nine chapters written by prominent experts in the field and discusses the disease concept, diagnosis and treatment, as well as recent findings on its pathogenesis and pathophysiology. As such, it offers an invaluable source of information for researchers and clinicians alike.
650 7 _aEnfermedades autoinmunes
_2embne
_0(OCoLC)fst00822663
_0
_9143353
700 1 _aOkazaki, Kazuichi,
_d1953-
_eeditor literario
_988975
856 4 0 _uhttps://go.openathens.net/redirector/universidadeuropea.es?url=http://link.springer.com/10.1007/978-3-319-52542-6
_zAcceso a este recurso digital (usuarios Universidad Europea de Madrid)
988 _aEBOOK, asignarmaterias, EBSPRINGER_2017C
998 _b02/2018
_dz
_e-
_zSI
999 _c95682
_d95682
_x1