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Open access Oct 2026

Vitamin D receptor gene variants and their association with clinical phenotypes of multiple sclerosis.

The investigated VDR variants do not appear to independently influence MS susceptibility, specific genotype combinations and alleles may contribute to the clinical expression of the disease, and the results support a potential role for vitamin D signalling in shaping MS heterogeneity.

V. Siokas, Athanassios Raptis, Danae Komodromou et al. · 0 citations
Review Open access Sep 2026

Therapeutic Applications of rTMS in Migraine Prophylaxis.

Migraine is one of the main causes of neurological disability, especially in young adults. Recent developments in preventive migraine therapies have improved outcomes for many patients, while highlighting the need for additional therapeutic options for those who remain refractory to pharmacological prophylaxis. Repetit...

V. Siokas, Chrysoula Marogianni, Ioannis Liampas et al. · 0 citations
Review Open access Aug 2026

Apolipoprotein E Alleles Across the Spectrum of Frontotemporal Lobar Degeneration: A Systematic Review and Meta-Analysis

We conducted a systematic review and meta-analysis of associations between apolipoprotein E (APOE) alleles and frontotemporal lobar degeneration (FTLD)-spectrum disorders. MEDLINE, Embase, CENTRAL, and Google Scholar were searched. APOE2 and APOE4 carrier status were compared between FTLD-spectrum disorders and healthy...

Ioannis Liampas, Antonis Polyviou, Silvia Demiri et al. · 0 citations

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