van den Ameele, J. ., Jedlickova, I. ., Pristoupilova, A. ., Sieben, A. ., Van Mossevelde, S. ., de Groote, C.-. ., … Dermaut, B. . (2018). Teenage-onset progressive myoclonic epilepsy due to a familial <i>C9orf72</i> repeat expansion. Neurology. https://doi.org/10.1212/WNL.0000000000004999 (Original work published 2018)
S Van Mossevelde
First name:
S
Last name:
Van Mossevelde
Sieben, A. ., Van Mossevelde, S. ., Wauters, E. ., Engelborghs, S. ., van der Zee, J. ., Van Langenhove, T. ., … Martin, J. . (2018). Extended FTLD pedigree segregating a Belgian GRN-null mutation: neuropathological heterogeneity in one family. Alzheimer’s Research & Therapy, 10(1), 7. https://doi.org/10.1186/s13195-017-0334-y (Original work published 2018)
