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Open access Aug 2026

Comparison of MRI sequences for optic nerve lesion detection in the follow-up of multiple sclerosis

Background: Optic nerve involvement is common in multiple sclerosis (MS) and is now recognized as a key site for dissemination in space under the most recent revision of McDonald's criteria. Reliable detection of optic nerve lesions is essential for diagnosis and monitoring, yet the optimal MRI sequence remains uncertain. Objective: To compare the diagnostic performance of three MRI sequences - short tau inversion recovery (STIR), fat-suppressed FLAIR (fs-FLAIR), and double inversion recovery (DIR)- in detecting optic nerve lesions in MS patients. Methods: Fifty-nine MS patients underwent MRI with STIR, fs-FLAIR, and DIR sequences and visual evoked potential (VEP) testing. Lesion detection was assessed independently for each sequence, and results were compared to structural and functional standards. Results: No significant differences were found in lesion detection across the three sequences. All sequences showed similar sensitivity to structural and functional changes. The incremental benefit of adding orbita specific sequence to a whole-brain sequence was limited in the follow-up of MS. Conclusion: In patients with established MS, whole-brain sequences (fs-FLAIR, DIR) perform comparably to dedicated orbital sequences (STIR) in detecting optic nerve lesions. This supports the feasibility of MRI protocols by omitting additional orbital sequences in routine follow-up, thereby reducing scan time and patient burden without compromising diagnostic sensitivity.

M. Csomós, M. Pribojszki, B. Loczi et al. · 0 citations
Open access Sep 2026

Mapping the dual functional organization of the substantia nigra.

The human substantia nigra (SN) is a central hub for dopaminergic signalling and a key site of pathology in Parkinson's disease (PD). However, its internal functional organization in human individuals is not well understood. To fill this knowledge gap, here we applied connectopic mapping to the SN in more than 1000 participants from four independent datasets. We identified two main gradients or axes of functional organization within the SN-a mediolateral and a posteroanterior-each showing distinct transcriptomic, behavioural, and pathological associations. Specifically, the mediolateral gradient was related to motor and executive functions, aging and α-synuclein pathology in both PD and Alzheimer's disease (AD). In contrast, the posteroanterior gradient was linked to memory, anxiety, depression and other neuropsychiatric symptoms in all cohorts. We found gradient-specific associations with gene expression profiles, neurotransmitter maps and cerebrospinal fluid biomarkers that further supported their neurobiological differences. Together, these results reveal a dual-gradient architecture that reflects the functional heterogeneity of the SN and offers new markers, grounded in behaviour and pathology, for stratifying neurodegenerative disease risk in aging, PD and AD.

D. Veréb, Blanca Zufiria-Gerbolés, M. Passaretti et al. · 0 citations

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