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Researcher
Tim Van Langenhove
Profile
Projects
Publications
Activities
Awards & Distinctions
30
Results
2024
De Nederlandstalige vertaling van de MoCA-HI : een cognitieve screeningstest voor personen met gehoorverlies
Katrien Kestens
Heleen Van Der Biest
Paul Corthals
Marijke Miatton
Marta Scarioni
Tineke Van Vrekhem
Bregje D'haeze
Tim Van Langenhove
Hannah Keppler
C3
Conference
2024
De Nederlandstalige vertaling van de MoCA-HI : een cognitieve screeningstest voor personen met gehoorverlies
Katrien Kestens
Heleen Van Der Biest
Paul Corthals
Marijke Miatton
Marta Scarioni
Tineke Van Vrekhem
Bregje D'haeze
Tim Van Langenhove
Hannah Keppler
A2
Journal Article
in
LOGOPEDIE (HERENTALS)
2024
Hearing-related quality of life in people with Alzheimer's disease
Katrien Kestens
Tim Van Langenhove
Marijke Miatton
Marta Scarioni
Tineke Van Vrekhem
Bregje D'haeze
Hannah Keppler
U
Conference
2024
2023
Exome sequencing and multigene panel testing in 1,411 patients with adult-onset neurologic disorders
Nika Schuermans
Hannah Verdin
Jody Ghijsels
Madeleine Hellemans
Elke Debackere
Elke Bogaert
Sofie Symoens
Leslie Naesens
Elien Lecomte
David Crosiers
et al.
A1
Journal Article
in
NEUROLOGY-GENETICS
2023
2022
HEARDEM : the importance of evaluating hearing in people with dementia
Katrien Kestens
Marijke Miatton
Tim Van Langenhove
Hannah Keppler
C3
Conference
2022
Therapy-induced electrophysiological changes in primary progressive aphasia : a preliminary study
Jara Stalpaert
Sofie Standaert
Lien D’Helft
Marijke Miatton
Anne Sieben
Tim Van Langenhove
Wouter Duyck
Pieter van Mierlo
Miet De Letter
A1
Journal Article
in
FRONTIERS IN HUMAN NEUROSCIENCE
2022
2021
A case series of verbal semantic processing in primary progressive aphasia : evidence from the N400 effect
Jara Stalpaert
Elissa-Marie Cocquyt
Marijke Miatton
Anne Sieben
Tim Van Langenhove
Pieter van Mierlo
Miet De Letter
A1
Journal Article
in
INTERNATIONAL JOURNAL OF LANGUAGE & COMMUNICATION DISORDERS
2021
GAD65 autoimmune encephalitis : a cause of rapidly evolving frontotemporal atrophy
Alexander Vanhoorne
Tim Van Langenhove
Marijke Miatton
Guy Laureys
A1
Journal Article
in
ALZHEIMER DISEASE & ASSOCIATED DISORDERS
2021
In-depth phenotypic description of TBK1 mutations ; a frequent cause of FTD and ALS in the Flanders-Belgian population
H Gossye
S Van Mossevelde
J Van der Zee
Y Vermeiren
N De Roeck
Jan De Bleecker
P Cras
P De Deyn
S Engelborghs
Tim Van Langenhove
et al.
C3
Conference
2021
The electrophysiological correlates of phoneme perception in primary progressive aphasia : a preliminary case series
Jara Stalpaert
Marijke Miatton
Anne Sieben
Tim Van Langenhove
Pieter van Mierlo
Miet De Letter
A1
Journal Article
in
FRONTIERS IN HUMAN NEUROSCIENCE
2021
2020
A genetic answer to a neuropsychiatric challenge
Hannah Dhaene
Céline Cousaert
Hannelore Tandt
Tim Van Langenhove
Marijke Miatton
Helena Gosseye
Gilbert Lemmens
Anne Sieben
A2
Journal Article
in
ACTA PSYCHIATRICA BELGICA
2020
Language and speech markers of primary progressive aphasia : a systematic review
Jara Stalpaert
Elissa-Marie Cocquyt
Yana Criel
Lieselot Segers
Marijke Miatton
Tim Van Langenhove
Pieter van Mierlo
Miet De Letter
A1
Journal Article
in
AMERICAN JOURNAL OF SPEECH-LANGUAGE PATHOLOGY
2020
2019
Clinical and electrophysiological markers of primary progressive aphasia : a systematic review
Jara Stalpaert
Elissa-Marie Cocquyt
Lieselot Segers
Tim Van Langenhove
Marijke Miatton
Pieter van Mierlo
Miet De Letter
C3
Conference
2019
Klinisch logopedische en elektrofysiologische markers van primair progressieve afasie : een systematische review
Jara Stalpaert
Elissa-Marie Cocquyt
Lieselot Segers
Tim Van Langenhove
Marijke Miatton
Pieter van Mierlo
Miet De Letter
C3
Conference
2019
2018
Clinical variability and onset age modifiers in an extended Belgian GRN founder family
Eline Wauters
Sara Van Mossevelde
Kristel Sleegers
Julie van der Zee
Sebastiaan Engelborghs
Anne Sieben
Rik Vandenberghe
Stephanie Philtjens
Marleen Van den Broeck
Karin Peeters
et al.
A1
Journal Article
in
NEUROBIOLOGY OF AGING
2018
2017
Clinical evidence of disease anticipation in families segregating a C9orf72 repeat expansion
Sara Van Mossevelde
Julie van der Zee
Ilse Gijselinck
Kristel Sleegers
Jan De Bleecker
Anne Sieben
Rik Vandenberghe
Tim Van Langenhove
Jonathan Baets
Olivier Deryck
et al.
A1
Journal Article
in
JAMA NEUROLOGY
2017
2016
Clinical features of TBKI carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort
Sara Van Mossevelde
Julie van der Zee
Ilse Gijselinck
Sebastiaan Engelborghs
Anne Sieben
Tim Van Langenhove
Jan De Bleecker
Jonathan Baets
Mathieu Vandenbulcke
Koen Van Laere
et al.
A1
Journal Article
in
BRAIN
2016
The C9orf72 repeat size correlates with onset age of disease, DNA methylation and transcriptional downregulation of the promoter
I Gijselinck
S Van Mossevelde
J van der Zee
Anne Sieben
S Engelborghs
Jan De Bleecker
A Ivanoiu
O Deryck
D Edbauer
M Zhang
et al.
A1
Journal Article
in
MOLECULAR PSYCHIATRY
2016
2015
Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brains
Jonathan Janssens
Stephanie Philtjens
Gernot Kleinberger
Sara Van Mossevelde
Julie van der Zee
Rita Cacace
Sebastiaan Engelborghs
Anne Sieben
Julia Banzhaf-Strathmann
Lubina Dillen
et al.
A1
Journal Article
in
ACTA NEUROPATHOLOGICA COMMUNICATIONS
2015
2014
Investigating the role of rare heterozygous TREM2 variants in Alzheimer's disease and frontotemporal dementia
Elise Cuyvers
Karolien Bettens
Stéphanie Philtjens
Tim Van Langenhove
Ilse Gijselinck
Julie van der Zee
Sebastiaan Engelborghs
Mathieu Vandenbulcke
Jasper Van Dongen
Nathalie Geerts
et al.
A1
Journal Article
in
NEUROBIOLOGY OF AGING
2014
Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration
Julie van der Zee
Tim Van Langenhove
Gabor G Kovacs
Lubina Dillen
William Deschamps
Sebastiaan Engelborghs
Radoslav Matěj
Mathieu Vandenbulcke
Anne Sieben
Bart Dermaut
et al.
A1
Journal Article
in
ACTA NEUROPATHOLOGICA
2014
2013
A pan-European study of the C9orf72 repeat associated with FTLD : geographic prevalence, genomic instability, and intermediate repeats
Julie van der Zee
Ilse Gijselinck
Lubina Dillen
Tim Van Langenhove
Jessie Theuns
Sebastiaan Engelborghs
Stéphanie Philtjens
Mathieu Vandenbulcke
Kristel Sleegers
Anne Sieben
et al.
A1
Journal Article
in
HUMAN MUTATION
2013
Distinct clinical characteristics of C9orf72 expansion carriers compared with GRN, MAPT, and nonmutation carriers in a Flanders-Belgian FTLD cohort
Tim Van Langenhove
Julie van der Zee
Ilse Gijselinck
Sebastiaan Engelborghs
Rik Vandenberghe
Mathieu Vandenbulcke
Jan De Bleecker
Anne Sieben
Jan Versijpt
Adrian Ivanoiu
et al.
A1
Journal Article
in
JAMA NEUROLOGY
2013
Explorative genetic study of UBQLN2 and PFN1 in an extended Flanders-Belgian cohort of frontotemporal lobar degeneration patients
Lubina Dillen
Tim Van Langenhove
Sebastiaan Engelborghs
Mathieu Vandenbulcke
Stayko Sarafov
Ivailo Tournev
Celine Merlin
Patrick Cras
Rik Vandenberghe
Peter P De Deyn
et al.
A1
Journal Article
in
NEUROBIOLOGY OF AGING
2013
2012
A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum : a gene identification study
Ilse Gijselinck
Tim Van Langenhove
Julie van der Zee
Kristel Sleegers
Stephanie Philtjens
Gernot Kleinberger
Jonathan Janssens
Karolien Bettens
Caroline Van Cauwenberghe
Sandra Pereson
et al.
A1
Journal Article
in
LANCET NEUROLOGY
2012
Ataxin-2 polyQ expansions in FTLD-ALS spectrum disorders in Flanders-Belgian cohorts
Tim Van Langenhove
Julie van der Zee
Sebastiaan Engelborghs
Rik Vandenberghe
Patrick Santens
Marleen Van den Broeck
Maria Mattheijssens
Karin Peeters
Dirk Nuytten
Patrick Cras
et al.
A1
Journal Article
in
NEUROBIOLOGY OF AGING
2012
Distinct clinical characteristics of C9orf72 expansion carriers compared to GRN, MAPT and non-mutation carries in a Flanders-Belgian FTLD cohort
Tim Van Langenhove
Julie van der Zee
Ilse Gijselinck
Sebastiaan Engelborghs
Rik Vandenberghe
Mathieu Vandenbulcke
Jan De Bleecker
Anne Sieben
Adrian Ivanoiu
Oliver Deryck
et al.
C3
Conference
2012
Identification of novel causal genes for frontotemporal lobar degeneration using whole genome sequencing
Stephanie Philtjens
Ilse Gijselinck
Tim Van Langenhove
Julie van der Zee
Sebastiaan Engelborgs
Rik Vandenberghe
Matthieu Vandenbulcke
Patrick Santens
Peter De Deyn
Christine Van Broeckhoven
et al.
C3
Conference
2012
The genetics and neuropathology of frontotemporal lobar degeneration
Anne Sieben
Tim Van Langenhove
Sebastiaan Engelborghs
Jean-Jacques Martin
Paul Boon
Patrick Cras
Peter-Paul De Deyn
Patrick Santens
Christine Van Broeckhoven
Marc Cruts
A1
Journal Article
in
ACTA NEUROPATHOLOGICA
2012
2011
TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohort
Julie van der Zee
Tim Van Langenhove
Gernot Kleinberger
Kristel Sleegers
Sebastiaan Engelborghs
Rik Vandenberghe
Patrick Santens
Marleen Van Den Broeck
Geert Joris
Jolien Brys
et al.
A1
Journal Article
in
BRAIN
2011