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Showing results for van mossevelde s[au]
Your search for VanMossevelde S[au] retrieved no results
Modifiers of GRN-Associated Frontotemporal Lobar Degeneration.
Wauters E, Van Mossevelde S, Van der Zee J, Cruts M, Van Broeckhoven C. Wauters E, et al. Among authors: van mossevelde s. Trends Mol Med. 2017 Oct;23(10):962-979. doi: 10.1016/j.molmed.2017.08.004. Epub 2017 Sep 7. Trends Mol Med. 2017. PMID: 28890134 Review.
Relationship between C9orf72 repeat size and clinical phenotype.
Van Mossevelde S, van der Zee J, Cruts M, Van Broeckhoven C. Van Mossevelde S, et al. Curr Opin Genet Dev. 2017 Jun;44:117-124. doi: 10.1016/j.gde.2017.02.008. Epub 2017 Mar 17. Curr Opin Genet Dev. 2017. PMID: 28319737 Free article. Review.
Tacrolimus-induced cognitive impairment: a case report.
Deprez V, Goeman J, Van Mossevelde S. Deprez V, et al. Among authors: van mossevelde s. Acta Neurol Belg. 2024 Jan 26. doi: 10.1007/s13760-023-02465-x. Online ahead of print. Acta Neurol Belg. 2024. PMID: 38277063 No abstract available.
Extended FTLD pedigree segregating a Belgian GRN-null mutation: neuropathological heterogeneity in one family.
Sieben A, Van Mossevelde S, Wauters E, Engelborghs S, van der Zee J, Van Langenhove T, Santens P, Praet M, Boon P, Miatton M, Van Hoecke S, Vandenbulcke M, Vandenberghe R, Cras P, Cruts M, De Deyn PP, Van Broeckhoven C, Martin JJ. Sieben A, et al. Among authors: van mossevelde s. Alzheimers Res Ther. 2018 Jan 22;10(1):7. doi: 10.1186/s13195-017-0334-y. Alzheimers Res Ther. 2018. PMID: 29370838 Free PMC article. Review.
Patients carrying the mutation p.R406W in MAPT present with non-conforming phenotypic spectrum.
Gossye H, Van Mossevelde S, Sieben A, Bjerke M, Hendrickx Van de Craen E, van der Zee J, De Deyn PP, De Bleecker J, Versijpt J, van den Ende J, Deryck O, Bourgeois P, Bier JC, Goethals M, Vandenberghe R, Engelborghs S, Van Broeckhoven C. Gossye H, et al. Among authors: van mossevelde s. Brain. 2023 Apr 19;146(4):1624-1636. doi: 10.1093/brain/awac362. Brain. 2023. PMID: 36171642 Free PMC article.
No association of CpG SNP rs9357140 with onset age in Belgian C9orf72 repeat expansion carriers.
Koçoğlu C, Gossye H, Dillen L, Van Mossevelde S, De Bleecker JL, Vandenberghe R, De Deyn PP, Sleegers K, Cras P, Engelborghs S, Van Broeckhoven C, van der Zee J; BELNEU Consortium. Koçoğlu C, et al. Among authors: van mossevelde s. Neurobiol Aging. 2021 Jan;97:145.e1-145.e4. doi: 10.1016/j.neurobiolaging.2020.07.021. Epub 2020 Aug 15. Neurobiol Aging. 2021. PMID: 32921502 Free article.
NEK1 genetic variability in a Belgian cohort of ALS and ALS-FTD patients.
Nguyen HP, Van Mossevelde S, Dillen L, De Bleecker JL, Moisse M, Van Damme P, Van Broeckhoven C, van der Zee J; BELNEU Consortium. Nguyen HP, et al. Among authors: van mossevelde s. Neurobiol Aging. 2018 Jan;61:255.e1-255.e7. doi: 10.1016/j.neurobiolaging.2017.08.021. Epub 2017 Aug 31. Neurobiol Aging. 2018. PMID: 28935222 Free article.
EEG Dominant Frequency Peak Differentiates Between Alzheimer's Disease and Frontotemporal Lobar Degeneration.
Goossens J, Laton J, Van Schependom J, Gielen J, Struyfs H, Van Mossevelde S, Van den Bossche T, Goeman J, De Deyn PP, Sieben A, Martin JJ, Van Broeckhoven C, van der Zee J, Engelborghs S, Nagels G. Goossens J, et al. Among authors: van mossevelde s. J Alzheimers Dis. 2017;55(1):53-58. doi: 10.3233/JAD-160188. J Alzheimers Dis. 2017. PMID: 27636837
Clinical variability and onset age modifiers in an extended Belgian GRN founder family.
Wauters E, Van Mossevelde S, Sleegers K, van der Zee J, Engelborghs S, Sieben A, Vandenberghe R, Philtjens S, Van den Broeck M, Peeters K, Cuijt I, De Coster W, Van Langenhove T, Santens P, Ivanoiu A, Cras P, De Bleecker JL, Versijpt J, Crols R, De Klippel N, Martin JJ, De Deyn PP, Cruts M, Van Broeckhoven C; Belgian Neurology (BELNEU) Consortium. Wauters E, et al. Among authors: van mossevelde s. Neurobiol Aging. 2018 Jul;67:84-94. doi: 10.1016/j.neurobiolaging.2018.03.007. Epub 2018 Mar 10. Neurobiol Aging. 2018. PMID: 29653316 Free article.
30 results