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期刊名:Autoimmunity highlights

缩写:AUTOIMMUN HIGHLIGHTS

ISSN:2038-0305

e-ISSN:2038-3274

IF/分区:0.0/

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共收录本刊相关文章索引146
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Carmen Gelpí,Elena Pérez,Cristina Roldan Carmen Gelpí
Purpose: The aim of this study was to compare the degree of agreement of a novel Zenit RA chemiluminescent immunoassay (CLIA) from A. Menarini Diagnostics (Florence, Italy) and the gold standard immunoprecipitation assay ...
D Squatrito,G Emmi,E Silvestri et al. D Squatrito et al.
Systemic lupus erythematosus (SLE) is considered an autoimmune disease with multiorgan involvement. Many advances have been made during the last decade regarding inflammatory pathways, genetic and epigenetic alterations, adaptive and innate...
Corrado Betterle,Silvia Garelli,Graziella Coco et al. Corrado Betterle et al.
Context: Type 3 autoimmune polyendocrine syndrome (APS-3) is defined by the presence of an autoimmune thyroid disease and another autoimmune illness, excluding Addison's disease; this is a frequent combination. ...
Beatrice Marinoni,Angela Ceribelli,Marco S Massarotti et al. Beatrice Marinoni et al.
Psoriasis and psoriatic arthritis represent two paradigmatic conditions characterized by chronic inflammation and possibly autoimmunity, despite the absence of known serum autoantibodies. The two diseases, albeit strongly correlated from cl...
Amedeo Amedei,Nicola Pimpinelli,Alessia Grassi et al. Amedeo Amedei et al.
Objective: To determine serum soluble CD30 (sCD30) levels in patients with graft versus host disease (GVHD). Methods: Serum soluble CD3...
Monica Galli Monica Galli
The antiphospholipid syndrome is characterized by a combination of laboratory findings (i.e., the presence of at least one antiphospholipid antibody) and clinical manifestations (arterial and/or venous thrombosis, obstetrical complications)...
Fatemeh Zare Shahneh,Fatemeh Hamzavi,Babak Bayazi et al. Fatemeh Zare Shahneh et al.
Behçet's syndrome (BS) is a chronic recurrent inflammatory disorder characterized by oral and genital ulcers and ocular inflammation. BS has a complex genetic etiology. To evaluate the influence of human leukocyte antigen (HLA) class I in ...
Petra M Pego,Inês Aguiar Câmara,José Pedro Andrade et al. Petra M Pego et al.
Introduction: Polyarteritis nodosa (PAN) is a systemic necrotizing medium-size-vessel vasculitis with variable clinical manifestations. Diagnosis is confirmed by histology or angiography. The mainstay of treatment is cort...
Periklis Vounotrypidis,Georgios Kouklakis,Konstantinos Anagnostopoulos et al. Periklis Vounotrypidis et al.
Purpose: This study aims to investigate any associations of the proinflammatory cytokine IL-1 in treated patients with inflammatory bowel disease (IBD) and the enteropathic seronegative spondylarthritis (eSpA). ...
Luiza Guilherme,Edilberto Postol,Frederico Moraes Ferreira et al. Luiza Guilherme et al.
Streptococcus pyogenes infections remain a health problem in multiple countries because of poststreptococcal sequelae, such as rheumatic fever and rheumatic heart disease. The epidemiological growth of streptococcal diseases in undeveloped ...