Sara Van Mossevelde

Antwerpen, VLG, Belgium

Last Updated: 09/26/2026

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Found 31 publications

Biomarker-Based Diagnosis and Care Pathways for Alzheimer's Disease in the Era of Disease-Modifying Treatments: A Consensus Statement by Belgian Experts.

Biomarker-Based Diagnosis and Care Pathways for Alzheimer's Disease in the Era of Disease-Modifying Treatments: A Consensus Statement by Belgian Experts.

Journal: European journal of neurology

Published: September 25, 2025

Diagnostic utility of electrophysiological markers for early and differential diagnosis of Alzheimer's, Frontotemporal, and Lewy Body dementias: A systematic review.

Diagnostic utility of electrophysiological markers for early and differential diagnosis of Alzheimer's, Frontotemporal, and Lewy Body dementias: A systematic review.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Published: October 15, 2024

Tacrolimus-induced cognitive impairment: a case report.

Tacrolimus-induced cognitive impairment: a case report.

Journal: Acta neurologica Belgica

Published: August 16, 2023

Patients carrying the mutation p.R406W in MAPT present with non-conforming phenotypic spectrum.

Patients carrying the mutation p.R406W in MAPT present with non-conforming phenotypic spectrum.

Journal: Brain : a journal of neurology

Published: February 15, 2022

Contribution of rare homozygous and compound heterozygous VPS13C missense mutations to dementia with Lewy bodies and Parkinson's disease.

Contribution of rare homozygous and compound heterozygous VPS13C missense mutations to dementia with Lewy bodies and Parkinson's disease.

Journal: Acta neuropathologica communications

Published: October 21, 2020

No association of CpG SNP rs9357140 with onset age in Belgian C9orf72 repeat expansion carriers.

No association of CpG SNP rs9357140 with onset age in Belgian C9orf72 repeat expansion carriers.

Journal: Neurobiology of aging

Published: June 12, 2020

Loss of DPP6 in neurodegenerative dementia: a genetic player in the dysfunction of neuronal excitability.

Loss of DPP6 in neurodegenerative dementia: a genetic player in the dysfunction of neuronal excitability.

Journal: Acta neuropathologica

Published: December 03, 2018

Association of short-term cognitive decline and MCI-to-AD dementia conversion with CSF, MRI, amyloid- and 18F-FDG-PET imaging.

Association of short-term cognitive decline and MCI-to-AD dementia conversion with CSF, MRI, amyloid- and 18F-FDG-PET imaging.

Journal: NeuroImage. Clinical

Published: September 13, 2018

Genotype-phenotype links in frontotemporal lobar degeneration.

Genotype-phenotype links in frontotemporal lobar degeneration.

Journal: Nature reviews. Neurology

Published: May 20, 2018

No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients.

No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients.

Journal: Neurobiology of aging

Published: March 22, 2018

Genetic screening in early-onset dementia patients with unclear phenotype: relevance for clinical diagnosis.

Genetic screening in early-onset dementia patients with unclear phenotype: relevance for clinical diagnosis.

Journal: Neurobiology of aging

Published: December 26, 2017

Clinical variability and onset age modifiers in an extended Belgian GRN founder family.

Clinical variability and onset age modifiers in an extended Belgian GRN founder family.

Journal: Neurobiology of aging

Published: November 09, 2017

Showing 1-12 of 31

Last Updated: 09/26/2026