UBA1 gene mutations are NOT always synonymous with #VEXAS syndrome. As such, #GRAI (Romanian Group for Autoinflammatory Diseases) presents a small reminder of the clinical phenotypes associated with UBA1 mutated genotypes, such as SMAX2 or lung cancer in never smokers.
Presented at #EULAR2026:
In a phase 3 trial, obexelimab led to a lower risk of disease flares than placebo among patients with IgG4-related disease. Glucocorticoid use was lower and the incidence of remission was higher with obexelimab than with placebo. Full INDIGO trial results: https://t.co/Lynf6nmA9N
Editorial: Obexelimab and the Promise of Nondepleting B-Cell Therapy in IgG4-Related Disease https://t.co/BUQ7r8jVWz
@eular_org
Congrats on this prospective study in @GreenJournal!
Beyond the striking finding that nearly half of rapidly progressive dementia etiologies were immune-mediated, it is a great example of how neurologists can generate meaningful data while doing clinical work👏🏽
Example to follow!
Great @NEJM review;
#Neurology should take note
Inflammatory myopathies are moving beyond antibody status to a pathophysiology-based understanding👇🏽
Inclusion Body → CD8+ T cells
Necrotizing or antisynthetase → pathogenic antibodies
Dermatomyositis → acquired interferonopathy
A breakthrough in anti-IgLON5 disease research: patient-derived autoantibodies directly trigger neuronal hyperactivity, abnormal Tau redistribution/phosphorylation, and neuroinflammation — establishing a causal link between autoimmunity and Tau pathology.
https://t.co/QUz8f2aJEn
Pragmatic. Full of information. Cutting edge. Cool figs!
Honored to lead The Lancet review on Encephalitis. With amazing Sophie B, Ava E, Kiran T & @DeannaSaylor1
We hope you enjoy reading it:
https://t.co/0baEHVhjeH
@mayoneurores@mayocliniclabs@MayoClinic@NDCNOxford
Inflammatory myopathies are typically associated with a myositis-specific autoantibody that determines the diagnosis and prognosis. Myositis subgroups have distinct pathomechanisms that now allow for targeted therapies.
Learn more in the Review Article “Inflammatory Myopathies” by Yves Allenbach, MD, PhD, and Olivier Benveniste, MD, PhD: https://t.co/ZeCKdNe87v
Every square tells a story - a new schema, a sharpened illness script, a diagnostic pivot, a moment of uncertainty transformed into insight.
A constant reminder that the best part of medicine is learning together.
@CPSolvers Academy 😇
@ASanchez_PS Substrate could be autonomic neuropathy/failure. In terms of causes: Parkinson's, amyloidosis, pure autonomic failure, neurogenic shoch from various acute causes.
Not all pulmonary emboli are thrombotic. NTPE includes septic, tumor, fat, air, and iatrogenic causes—often mimicking PE but needing different management. Imaging clues and clinical context are key for timely diagnosis. @BrighamRad@BWHRadEdu https://t.co/ASxSrgdXoh
🚨🧠 happening now: exciting session on CAA on the intersection between stroke, neurodegeneration x neuroinflammation covering a large spectrum of CAA from ICH to degeneration, neuroinflammation, iatrogenic forms and back! Thought provoking session. #ESOC2026
📅 Mark your calendars for the 25th European Congress of Internal Medicine (ECIM 2027)!
🗓 31 March – 3 April 2027
📍Paris, France 🇫🇷
Integrating Evidence Based and Personalised Medicine in the heart of France.
Stay tuned👉https://t.co/EKWbHK8POg
#ECIM2027#Paris