Bart Dermaut

Gent, VLG 9000, Belgium

Last Updated: 09/26/2026

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Found 40 publications

Upper limb freezing, palilalia and tachyphemia in atypical Pantothenate kinase-associated neurodegeneration.

Upper limb freezing, palilalia and tachyphemia in atypical Pantothenate kinase-associated neurodegeneration.

Journal: Parkinsonism & related disorders

Published: December 18, 2025

Genetic Landscape of Monogenic Parkinson's Disease in the African Population-A Systematic Review.

Genetic Landscape of Monogenic Parkinson's Disease in the African Population-A Systematic Review.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: December 10, 2025

Increased plasma fibronectin mirrors intimal phenotypic switching of vascular smooth muscle cells in moyamoya arteriopathy.

Increased plasma fibronectin mirrors intimal phenotypic switching of vascular smooth muscle cells in moyamoya arteriopathy.

Journal: Scientific reports

Published: September 10, 2025

Myopathic aggregation-prone variants in the TDP-43 prion-like domain: genetics paving the way.

Myopathic aggregation-prone variants in the TDP-43 prion-like domain: genetics paving the way.

Journal: Brain : a journal of neurology

Published: September 03, 2024

Pooled analysis of patients with inherited prion disease caused by two- to twelve-octapeptide repeat insertions in the prion protein gene (PRNP).

Pooled analysis of patients with inherited prion disease caused by two- to twelve-octapeptide repeat insertions in the prion protein gene (PRNP).

Journal: Journal of neurology

Published: July 19, 2023

C-terminal frameshift variant of TDP-43 with pronounced aggregation-propensity causes rimmed vacuole myopathy but not ALS/FTD.

C-terminal frameshift variant of TDP-43 with pronounced aggregation-propensity causes rimmed vacuole myopathy but not ALS/FTD.

Journal: Acta neuropathologica

Published: December 29, 2022

Loss of phospholipase PLAAT3 causes a mixed lipodystrophic and neurological syndrome due to impaired PPARγ signaling.

Loss of phospholipase PLAAT3 causes a mixed lipodystrophic and neurological syndrome due to impaired PPARγ signaling.

Journal: Nature genetics

Published: December 22, 2022

SRSF1 haploinsufficiency is responsible for a syndromic developmental disorder associated with intellectual disability.

SRSF1 haploinsufficiency is responsible for a syndromic developmental disorder associated with intellectual disability.

Journal: American journal of human genetics

Published: December 14, 2022

Exome Sequencing and Multigene Panel Testing in 1,411 Patients With Adult-Onset Neurologic Disorders.

Exome Sequencing and Multigene Panel Testing in 1,411 Patients With Adult-Onset Neurologic Disorders.

Journal: Neurology. Genetics

Published: October 19, 2022

Marked hypotonia: An additional feature of ANO3-related movement disorder.

Marked hypotonia: An additional feature of ANO3-related movement disorder.

Journal: European journal of medical genetics

Published: May 30, 2022

Tau promotes oxidative stress-associated cycling neurons in S phase as a pro-survival mechanism: Possible implication for Alzheimer's disease.

Tau promotes oxidative stress-associated cycling neurons in S phase as a pro-survival mechanism: Possible implication for Alzheimer's disease.

Journal: Progress in neurobiology

Published: May 23, 2022

Moyamoya disease emerging as an immune-related angiopathy.

Moyamoya disease emerging as an immune-related angiopathy.

Journal: Trends in molecular medicine

Published: May 20, 2022

Showing 1-12 of 40

Last Updated: 09/26/2026