Research output per year
Research output per year
Personal profile
Research interests
Neuromuscular disorders: motor neuron disease, hereditary neuropathies, inflammatory myopathies
Specialisation
Neurology and in particular Neuromuscular Disorders
Network
Recent external collaboration on country/territory level. Dive into details by clicking on the dots or
-
Clinical spectrum time course in non-Asian patients positive for anti-MDA5 antibodies
AENEAS collaborative group, 1 Feb 2022, In: Clinical and experimental rheumatology. 40, 2, p. 274-283 10 p.Research output: Contribution to journal › Article* › Academic › peer-review
Open Access -
Cortical and subcortical changes in resting-state neuronal activity and connectivity in early symptomatic ALS and advanced frontotemporal dementia
Govaarts, R., Beeldman, E., Fraschini, M., Griffa, A., Engels, M. M. A., van Es, M. A., Veldink, J. H., van den Berg, L. H., van der Kooi, A. J., Pijnenburg, Y. A. L., de Visser, M., Stam, C. J., Raaphorst, J. & Hillebrand, A., 1 Jan 2022, In: NeuroImage: Clinical. 34, 102965.Research output: Contribution to journal › Article* › Academic › peer-review
Open Access -
Editorial: Palliative Care in Neurology, Volume II
Oliver, D., de Visser, M. & Voltz, R., 16 Feb 2022, In: Frontiers in Neurology. 13, 840110.Research output: Contribution to journal › Editorial* › Academic › peer-review
Open Access -
European Academy of Neurology guidance for developing and reporting clinical practice guidelines on rare neurological diseases
Aleksovska, K., Kobulashvili, T., Costa, J., Zimmermann, G., Ritchie, K., Reinhard, C., Vignatelli, L., Fanciulli, A., Damian, M., Pavlakova, L., Burgunder, J-M., Kopishinskaya, S., Rakusa, M., Kovacs, N., Erdogan, F. F., Linton, L. R., Copetti, M., Lamperti, C., Servidei, S., Evangelista, T. & 15 others, , Jun 2022, In: European journal of neurology. 29, 6, p. 1571-1586 16 p.Research output: Contribution to journal › Article* › Academic › peer-review
-
High-resolution breakpoint junction mapping of proximally extended D4Z4 deletions in FSHD1 reveals evidence for a founder effect
Lemmers, R. J. L. F., van der Vliet, P. J., Granado, D. S. L., van der Stoep, N., Buermans, H., van Schendel, R., Schimmel, J., de Visser, M., van Coster, R., Jeanpierre, M., Laforet, P., Upadhyaya, M., van Engelen, B., Sacconi, S., Tawil, R., Voermans, N. C., Rogers, M. & van der Maarel, S. M., 1 Mar 2022, In: Human Molecular Genetics. 31, 5, p. 748-760 13 p.Research output: Contribution to journal › Article* › Academic › peer-review