272nd ENMC international workshop: 10 Years of progress - revision of the ENMC 2013 diagnostic criteria for inclusion body myositis and clinical trial readiness. 16–18 June 2023, Hoofddorp, The Netherlands

Lilleker, J. B., Naddaf, E., Saris, C. G. J., Schmidt, J., de Visser, M., Weihl, C. C., Alexandersson, H., Alfano, L., Allenbach, Y., Badrising, U., Benveniste, O., Bhai, S., de Bleecker, J., Breeveld, M. C., Chinoy, H., Diederichsen, L., Dimachkie, M., Greenberg, S., Johari, M., Lilleker, J., & 12 othersLindgren, U., Lloyd, T., Machado, P., Mozaffar, T., Mischke, R., Needham, M., Nishino, I., Oldfors, A., Saris, C., Stenzel, W., Tasca, G. & the 272nd ENMC workshop participants, 1 Apr 2024, In: Neuromuscular disorders. 37, p. 36-51 16 p.

Research output: Contribution to journal › Article › Academic › peer-review

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

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 othersEng, C., Lamy, F., Plançon, J-P., Haberlova, J., Brusse, E., Hoeijmakers, J. G. J., de Visser, M., Claeys, K. G., Paradas, C., Toscano, A., Silani, V., Gyenge, M., Reviers, E., Hamroun, D., Vroom, E., Wilkinson, M. D., Lochmuller, H. & Evangelista, T., 1 Dec 2024, In: Orphanet Journal of Rare Diseases. 19, 1, 66.

Research output: Contribution to journal › Review article › Academic › peer-review

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., 2024, (E-pub ahead of print) In: European journal of neurology.

Research output: Contribution to journal › Editorial › Academic › peer-review

Performance of the 2017 EULAR/ACR Classification Criteria for adult and juvenile idiopathic inflammatory myopathies and their major subgroups: a scoping review

Saygin, D., Glaubitz, S., Zeng, R., Bottai, M., de Visser, M., Dimachkie, M. M., Fiorentino, D., Gerhardson, I., Kuwana, M., Miller, F. W., Needham, M., Rider, L. G., Salem, Y., Schlüter, S., Shinjo, S. K., Wang, G., Werth, V. P., Aggarwal, R. & Lundberg, I. E., 1 Feb 2024, In: Clinical and experimental rheumatology. 42, 2, p. 403-412 10 p.

Research output: Contribution to journal › Review article › Academic › peer-review