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)
