Author

L. Wolff

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Open access Aug 2026

Clinical Spectrum, Treatments and Outcomes of VEXAS Syndrome: A Multicenter Belgian Cohort

Background VEXAS syndrome is a late onset autoinflammatory disease caused by somatic UBA1 mutations and characterized by heterogeneous systemic and hematologic manifestations. We aimed to describe all identified Belgian cases through a national multicenter cohort. Methods We conducted a retrospective study across four...

L. Funaro, L. Naesens, A. Betrains et al. · medRxiv · 0 citations

Aug 2026

[Anti-LGI1 antibody encephalitis: A monocentric retrospective series of seven patients].

Anti-leucine-rich glioma-inactivated 1 (LGI1) autoimmune encephalitis is a rare neurological disorder caused by autoantibodies targeting the LGI1 protein, leading to synaptic dysfunction predominantly affecting the temporal lobes and hippocampi. It is mainly characterized by cognitive impairment, focal seizures, and fa...

L. Wolff, Mathieu Zuber, V. Roubeau · La Revue de medecine interne · 0 citations