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Acta Neurologica Belgica|June 25, 2026
Rare Listeria monocytogenes brain abscess presenting as a tunnel-like lesion in an immunocompromised patientTeymine Andreasyan, Tim Vanderhasselt
Journal of the Belgian Society of Radiology|February 23, 2023
Unusual Lesion in the Splenium of the Corpus Callosum and COVID-19 Infection: A Case ReportWiem Abid, Tim Vanderhasselt, Gert-Jan Allemeersch
BMC Medical Imaging|April 8, 2021
Detection of parathyroid adenomas with multiphase 4DCT: towards a true four-dimensional techniqueSteven Raeymaeckers, Yannick De Brucker, Tim Vanderhasselt, et al.
AJNR. American Journal of Neuroradiology|December 12, 2025
Internal Cerebral Vein Doppler Velocities Reflect Maturational Changes and Hemorrhage Risk in Preterm InfantsFleur A Camfferman, Paul Govaert, Floris Groenendaal, et al.
Frontiers in Systems Neuroscience|January 14, 2017
Interhemispheric Connections between the Primary Visual Cortical Areas via the Anterior Commissure in Human Callosal AgenesisNathalie van Meer, Anne C Houtman, Peter Van Schuerbeek, et al.
BMC Geriatrics|June 20, 2020
Leptomeningeal metastasis in a marginal zone lymphoma, presenting as a delirium: case reportLisa Dreessen, Nicolas Maréchal, Michel Verheyden, et al.
Physiotherapy|August 9, 2011
Postmastectomy lymphoedema: different patterns of fluid distribution visualised by ultrasound imaging compared with magnetic resonance imagingAn Tassenoy, Johan De Mey, Filip De Ridder, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 7, 2014
Thin genu of the corpus callosum points to mutation in FOXG1 in a child with acquired microcephaly, trigonocephaly, and intellectual developmental disorder: a case report and review of literatureCaroline De Bruyn, Tim Vanderhasselt, Ibrahim Tanyalçin, et al.
Neuroimage. Clinical|January 1, 2021
Synthetic MRI demonstrates prolonged regional relaxation times in the brain of preterm born neonates with severe postnatal morbidityTim Vanderhasselt, Roya Zolfaghari, Maarten Naeyaert, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 13, 2013
Elaborating the phenotypic spectrum associated with mutations in ARFGEF2: case study and literature reviewIbrahim Tanyalçin, Helene Verhelst, Dicky J J Halley, et al.
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