Specialization
Neurology and in particular Neuromuscular Disorders
Focus of research
Neuromuscular disorders: motor neuron disease, hereditary neuropathies, inflammatory myopathies
Amsterdam Neuroscience
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Correction to: A double-blind, placebo-controlled, randomized trial of PXT3003 for the treatment of Charcot–Marie–Tooth type 1A (Orphanet Journal of Rare Diseases, (2021), 16, 1, (433), 10.1186/s13023-021-02040-8)
Attarian, S., Young, P., Brannagan, T. H., Adams, D., van Damme, P., Thomas, F. P., Casanovas, C., Kafaie, J., Tard, C. L., Walter, M. C., Péréon, Y., Walk, D., Stino, A., de Visser, M., Verhamme, C., Amato, A., Carter, G., Magy, L., Statland, J. M. & Felice, K., 1 Dec 2024, In: Orphanet Journal of Rare Diseases. 19, 1, 142.Research output: Contribution to journal › Comment/Letter to the editor › Academic
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EURO-NMD registry: federated FAIR infrastructure, innovative technologies and concepts of a patient-centred registry for rare neuromuscular disorders
Atalaia, A., Wandrei, D., Lalout, N., Thompson, R., Tassoni, A., ’t Hoen, P. A. C., Athanasiou, D., Baker, S-A., Sakellariou, P., Paliouras, G., D’Angelo, C., Horvath, R., Mancuso, M., van der Beek, N., Kornblum, C., Kirschner, J., Pareyson, D., Bassez, G., Blacas, L., Jacoupy, M., & 18 others, 1 Dec 2024, In: Orphanet Journal of Rare Diseases. 19, 1, 66.Research output: Contribution to journal › Review article › Academic › peer-review
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Multidisciplinary management and care in rare neuromuscular disorders: A call for action
Ørstavik, K., Rosenberger, A. D., Fossmo, H. L., Nordstrøm, M. & de Visser, M., Jun 2024, In: European journal of neurology. 31, 6, e16265.Research output: Contribution to journal › Editorial › Academic › peer-review
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