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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2010 1
2011 1
2013 4
2014 4
2016 1
2017 1
2018 2
2019 4
2020 8
2021 4
2022 1
2023 2
2024 1

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24 results

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Page 1
Fourth ventricle papilloma and intractable cough.
Wiels WA, Geens W, Vanderhasselt T, Michotte A, Van Velthoven V. Wiels WA, et al. Among authors: vanderhasselt t. Acta Neurol Belg. 2020 Jun;120(3):751-753. doi: 10.1007/s13760-019-01249-6. Epub 2019 Nov 20. Acta Neurol Belg. 2020. PMID: 31745847 No abstract available.
Expanding the clinical spectrum of biallelic ZNF335 variants.
Stouffs K, Stergachis AB, Vanderhasselt T, Dica A, Janssens S, Vandervore L, Gheldof A, Bodamer O, Keymolen K, Seneca S, Liebaers I, Jayaraman D, Hill HE, Partlow JN, Walsh CA, Jansen AC. Stouffs K, et al. Among authors: vanderhasselt t. Clin Genet. 2018 Aug;94(2):246-251. doi: 10.1111/cge.13260. Epub 2018 May 3. Clin Genet. 2018. PMID: 29652087 Free PMC article.
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.
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.
Polymicrogyria with dysmorphic basal ganglia? Think tubulin!
Amrom D, Tanyalçin I, Verhelst H, Deconinck N, Brouhard GJ, Décarie JC, Vanderhasselt T, Das S, Hamdan FF, Lissens W, Michaud JL, Jansen AC. Amrom D, et al. Among authors: vanderhasselt t. Clin Genet. 2014 Feb;85(2):178-83. doi: 10.1111/cge.12141. Epub 2013 Apr 24. Clin Genet. 2014. PMID: 23495813
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.
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.
Abnormal primary gyration in relation to deep brain injury in preterm infants.
De Bisschop B, Camfferman F, van Hengel-Jacobs M, Delanghe G, Vanderhasselt T, Govaert P. De Bisschop B, et al. Among authors: vanderhasselt t. Acta Paediatr. 2020 Jan;109(1):204-205. doi: 10.1111/apa.14996. Epub 2019 Nov 8. Acta Paediatr. 2020. PMID: 31483907 No abstract available.
24 results