Explore the latest in inflammatory CNS disorders, including advances in diagnosis and treatment of paraneoplastic and autoimmune encephalitides.
This case-control study develops and evaluates a set of diagnostic criteria for Vogt-Koyanagi-Harada disease, an immune-mediated disorder affecting both eyes, using data from Chinese patients.
This Viewpoint examines the use of tocilizumab as glucocorticoid-sparing treatment in patients with giant cell arteritis.
The case series describes myelin oligodendrocyte glycoprotein IgG– and aquaporin 4 IgG–associated disease in 134 English patients who presented with seizure.
This cross-sectional study evaluates structural changes noted on neuroimaging and cognitive outcomes in patients with leucine-rich, glioma-inactivated 1 protein encephalitis.
A man in his 40s had a 1-year history of decreased vision and the sensation of tunnel vision, as well as cognitive decline for the past 2 years; he had undergone left nephrectomy 1 year prior for renal cell carcinoma, with no recurrence. What would you do next?
This case report describes a man in his 20s who was admitted with a clinical demyelination syndrome and a recent diagnosis of dengue fever.
This study describes a novel IgG autoantibody found in serum or cerebrospinal fluid that is specific for a cytosolic intermediate filament protein of astrocytes.
This study discusses the association between levels of high-sensitivity C-reactive protein and general psychological distress symptoms.
This meta-analysis quantitatively summarizes data on peripheral inflammatory cytokines in patients with Parkinson disease.
This case series describes 2 women with anti-N-methyl-d-aspartate receptor (anti-NMDAR) encephalitis whose disease remitted with bortezomib treatment.
This case series describes the clinical and radiographic characteristics of patients with anti–contactin-associated protein-like 2 (CASPR2) antibodies in their cerebrospinal fluid.
This study uses UK national survey data to investigate the association between C-reactive protein levels and risk of suicide.
This case report describes a 57-year-old man with hemochromatosis and panhypopituitarism who presented with a 6-month history of word-finding difficulty, short-term memory loss, and rapidly cycling symptoms.
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