Diagnostic technology is rapidly evolving, and over the last decade, substantial progress has been made even for the identification of antibodies, increasingly approaching this type of diagnostic to that of automated clinical chemistry laboratory. In this review, we describe the analytical and diagnostic characteristics of chemiluminescence technology in its strength and in its applicability for…
Autoimmunity Highlights Template
Write in a clean editor, then format for Autoimmunity Highlights in one click — DocuGuru applies the official Springer Nature template with numbered references and exports a submission-ready PDF plus the editable LaTeX source. Free to start.
About the Autoimmunity Highlights format
Autoimmunity Highlights is a peer-reviewed journal published by Springer Nature, covering Systemic Lupus Erythematosus Research, Monoclonal and Polyclonal Antibodies Research, Diabetes and associated disorders.
| Publisher | Springer Nature |
|---|---|
| Reference style | Numbered (Springer Basic) Numbered — [1], [2] in the text 1. Smith A, Jones B, Lee C (2023) A representative article title. Autoimmunity Highlights 12:45–58
Formats any DOI in Autoimmunity Highlights style. No sign-up. |
| Publishes research in | Systemic Lupus Erythematosus Research Monoclonal and Polyclonal Antibodies Research Diabetes and associated disorders T-cell and B-cell Immunology Liver Diseases and Immunity |
| ISSN | 2038-0305 |
| h-index | 35 |
| i10-index | 105 |
| Total citations | 4,664 |
| Open access | Yes |
| Top institutions publishing here | University of Thessaly |
| Journal website | link.springer.com |
| You get | A submission-ready PDF and the editable LaTeX source — ready to submit. |
Papers published in Autoimmunity Highlights per year
Citation impact of Autoimmunity Highlights by publication year
Citations each year’s papers have accumulated so far — the most recent years are still building up.
Most-cited papers in Autoimmunity Highlights
The gold standard to characterize idiopathic inflammatory myopathies is the morphological, immunohistochemical and immunopathological analysis of muscle biopsy. Mononuclear cell infiltrates and muscle fiber necrosis are commonly shared histopathological features. Inflammatory cells that surround, invade and destroy healthy muscle fibers expressing MHC class I antigen are the typical pathological finding of polymyositis. Perifascicular atrophy and…
Behçet's disease, also known as the Silk Road Disease, is a rare systemic vasculitis disorder of unknown etiology. Recurrent attacks of acute inflammation characterize Behçet's disease. Frequent oral aphthous ulcers, genital ulcers, skin lesions and ocular lesions are the most common manifestations. Inflammation is typically self-limiting in time and relapsing episodes of clinical manifestations represent…
The clinical success of anti-CD20 monoclonal antibody (mAb)-mediated B cell depletion therapy has contributed to the understanding of B cells as major players in several autoimmune diseases. The first therapeutic anti-CD20 mAb, rituximab, is a murine-human chimera to which many patients develop antibodies and/or experience infusion-related reactions. A second generation of anti-CD20 mAbs has been…
Multiple sclerosis (MS) is an immune-mediated disease of the central nervous system characterized by focal or diffuse inflammation, demyelination, axonal loss and neurodegeneration. Brain atrophy can be seen in the earliest stages of MS, progresses faster compared to healthy adults, and is a reliable predictor of future physical and cognitive disability. In addition, it is…