Jolien Perneel
Antwerpen, VLG, Belgium
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 13 publications
White matter pathology in FTLD caused by GRN mutations.
Journal: Acta neuropathologica
Published: November 05, 2024
Increased TMEM106B levels lead to lysosomal dysfunction which affects synaptic signaling and neuronal health.
Journal: Molecular neurodegeneration
Published: August 28, 2024
Accumulation of TMEM106B C-terminal fragments in Niemann-Pick type C disease.
Journal: Journal of neuropathology and experimental neurology
Published: July 04, 2024
Limbic-predominant age-related TDP-43 proteinopathy (LATE-NC) is associated with abundant TMEM106B pathology.
Journal: Acta neuropathologica
Published: March 13, 2023
Case report: TMEM106B haplotype alters penetrance of GRN mutation in frontotemporal dementia family.
Case report: TMEM106B haplotype alters penetrance of GRN mutation in frontotemporal dementia family.
Journal: Frontiers in neurology
Published: February 06, 2023
Correction to: Accumulation of TMEM106B C‑terminal fragments in neurodegenerative disease and aging.
Correction to: Accumulation of TMEM106B C‑terminal fragments in neurodegenerative disease and aging.
Journal: Acta neuropathologica
Published: January 06, 2023
C-terminal TMEM106B fragments in human brain correlate with disease-associated TMEM106B haplotypes.
Journal: Brain : a journal of neurology
Published: December 13, 2022
Accumulation of TMEM106B C-terminal fragments in neurodegenerative disease and aging.
Journal: Acta neuropathologica
Published: October 24, 2022
Homotypic fibrillization of TMEM106B across diverse neurodegenerative diseases.
Journal: Cell
Published: January 25, 2022
The Secretome of Filarial Nematodes and Its Role in Host-Parasite Interactions and Pathogenicity in Onchocerciasis-Associated Epilepsy.
Journal: Frontiers in cellular and infection microbiology
Published: February 01, 2021
Last Updated: 09/26/2026