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Encephalitis associated with the SARS-CoV-2 virus: A case report.
Vandervorst F, Guldolf K, Peeters I, Vanderhasselt T, Michiels K, Berends KJ, Van Laethem J, Pipeleers L, Vincken S, Seynaeve L, Engelborghs S. Vandervorst F, et al. Among authors: vanderhasselt t. Interdiscip Neurosurg. 2020 Dec;22:100821. doi: 10.1016/j.inat.2020.100821. Epub 2020 Jul 10. Interdiscip Neurosurg. 2020. PMID: 32835017 Free PMC article.
Inter- and Intra-Scanner Variability of Automated Brain Volumetry on Three Magnetic Resonance Imaging Systems in Alzheimer's Disease and Controls.
Wittens MMJ, Allemeersch GJ, Sima DM, Naeyaert M, Vanderhasselt T, Vanbinst AM, Buls N, De Brucker Y, Raeymaekers H, Fransen E, Smeets D, van Hecke W, Nagels G, Bjerke M, de Mey J, Engelborghs S. Wittens MMJ, et al. Among authors: vanderhasselt t. Front Aging Neurosci. 2021 Oct 7;13:746982. doi: 10.3389/fnagi.2021.746982. eCollection 2021. Front Aging Neurosci. 2021. PMID: 34690745 Free PMC article.
Towards validation in clinical routine: a comparative analysis of visual MTA ratings versus the automated ratio between inferior lateral ventricle and hippocampal volumes in Alzheimer's disease diagnosis.
Wittens MMJ, Allemeersch GJ, Sima DM, Vanderhasselt T, Raeymaeckers S, Fransen E, Smeets D, de Mey J, Bjerke M, Engelborghs S. Wittens MMJ, et al. Among authors: vanderhasselt t. Neuroradiology. 2024 Apr;66(4):487-506. doi: 10.1007/s00234-024-03280-8. Epub 2024 Jan 19. Neuroradiology. 2024. PMID: 38240767 Free PMC article.
Overlapping cortical malformations in patients with pathogenic variants in GRIN1 and GRIN2B.
Brock S, Laquerriere A, Marguet F, Myers SJ, Hongjie Y, Baralle D, Vanderhasselt T, Stouffs K, Keymolen K, Kim S, Allen J, Shaulsky G, Chelly J, Marcorelle P, Aziza J, Villard L, Sacaze E, de Wit MCY, Wilke M, Mancini GMS, Hehr U, Lim D, Mansour S, Traynelis SF, Beneteau C, Denis-Musquer M, Jansen AC, Fry AE, Bahi-Buisson N. Brock S, et al. Among authors: vanderhasselt t. J Med Genet. 2023 Feb;60(2):183-192. doi: 10.1136/jmedgenet-2021-107971. Epub 2022 Apr 7. J Med Genet. 2023. PMID: 35393335 Free PMC article.
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 literature.
De Bruyn C, Vanderhasselt T, Tanyalçin I, Keymolen K, Van Rompaey KL, De Meirleir L, Jansen AC. De Bruyn C, et al. Among authors: vanderhasselt t. Eur J Paediatr Neurol. 2014 May;18(3):420-6. doi: 10.1016/j.ejpn.2013.11.010. Epub 2013 Dec 6. Eur J Paediatr Neurol. 2014. PMID: 24388699 Review.
Defining the phenotypical spectrum associated with variants in TUBB2A.
Brock S, Vanderhasselt T, Vermaning S, Keymolen K, Régal L, Romaniello R, Wieczorek D, Storm TM, Schaeferhoff K, Hehr U, Kuechler A, Krägeloh-Mann I, Haack TB, Kasteleijn E, Schot R, Mancini GMS, Webster R, Mohammad S, Leventer RJ, Mirzaa G, Dobyns WB, Bahi-Buisson N, Meuwissen M, Jansen AC, Stouffs K. Brock S, et al. Among authors: vanderhasselt t. J Med Genet. 2021 Jan;58(1):33-40. doi: 10.1136/jmedgenet-2019-106740. Epub 2020 Jun 22. J Med Genet. 2021. PMID: 32571897 Free PMC article.
24 results