J.G.J. Hoeijmakers

Kool, D., Hoeijmakers, J. G. J., Faber, C. G., & Merkies, I. S. J. (2025). Where Does It All Itch? Exploring the Characteristics of Pruritus in Small Fiber Neuropathy. Journal of the Peripheral Nervous System, 30(3), Article e70041. https://doi.org/10.1111/jns.70041

van Tienen, F. H. J., Hoeijmakers, J. G. J., van der Leij, C., Timmer, E., Wanders, N., Lindsey, P. J., Yi, F., Lin, F., Kortekaas, S. P. M., Roelofs, H., Westra, I. M., Meij, P., Wijnen, L. A. C. M., de Coo, I. F. M., & Smeets, H. J. M. (2025). Intra-arterial transplantation of autologous mesoangioblasts in m.3243A>G mutation carriers is safe - first phase I/II human clinical study. Molecular Therapy. Advance online publication. https://doi.org/10.1016/j.ymthe.2025.07.005

Mané-Damas, M., Schöttler, A. K., Marcuse, F., Molenaar, P., Mohile, T., Hoeijmakers, J., Hochstenbag, M., Damoiseaux, J., Maessen, J., Abdul-Hamid, M., Zur Hausen, A., de Baets, M., Losen, M., & Martinez-Martinez, P. (2025). Myasthenia gravis with antibodies against the AChR, current knowledge on pathophysiology and an update on treatment strategies with special focus on targeting plasma cells. Autoimmunity Reviews, 24(10), Article 103875. Advance online publication. https://doi.org/10.1016/j.autrev.2025.103875

Rouvroye, M. D., Warendorf, J., Vrancken, A., Eftimov, F., Wieske, L., Faber, C. G., Hoeijmakers, J. G. J., Damoiseaux, J., van de Warrenburg, B., van Gaalen, J., van der Molen, R., Bouma, G., & Bontkes, H. (2025). Serological analysis of gluten-related antibodies in idiopathic neuropathies and cerebellar ataxia. Journal of Neurology, 272(7), Article 447. https://doi.org/10.1007/s00415-025-13187-w

Damci, A., den Hollander, M., Hoeijmakers, J. G. J., Faber, C. G., Goossens, M. E. J. B., & Verbunt, J. A. M. C. F. (2024). Biopsychosocial rehabilitation therapy in small fiber neuropathy: research protocol to study the effect of rehabilitation treatment. Frontiers in Neurology, 15, Article 1493326. https://doi.org/10.3389/fneur.2024.1493326

Misra, K., Sleczkowska, M., Santoro, S., Gerrits, M. M., Mascia, E., Marchi, M., Salvi, E., Smeets, H. J. M., Hoeijmakers, J. G. J., Boneschi, F. G. M., Filippi, M., Pinter, G. L., Faber, C. G., & Esposito, F. (2024). Broadening the Genetic Spectrum of Painful Small-Fiber Neuropathy through Whole-Exome Study in Early-Onset Cases. International Journal of Molecular Sciences, 25(13), Article 7248. https://doi.org/10.3390/ijms25137248

Geerts, M., Hoeijmakers, J. G. J., Essers, B. A. B., Merkies, I. S. J., Faber, C. G., & Goossens, M. E. J. B. (2024). Development, validation and feasibility of a Patient Satisfaction Questionnaire for evaluating the quality performance of a diagnostic small fibre neuropathy service: A qualitative study. Health Expectations, 27(2), Article e14011. https://doi.org/10.1111/hex.14011

Geerts, M., Hoeijmakers, J. G. J., Essers, B. A. B., Merkies, I. S. J., Faber, C. G., & Goossens, M. E. J. B. (2024). Patient satisfaction and patient accessibility in a small fiber neuropathy diagnostic service in the Netherlands: A single-center, prospective, survey-based cohort study. PLOS ONE, 19(4), Article e0298881. https://doi.org/10.1371/journal.pone.0298881

van Gool, R., Far, A., Drenthen, G. S., Jansen, J. F. A., Goijen, C. P., Backes, W. H., Linden, D. E. J., Merkies, I. S. J., Faber, C. G., Upadhyay, J., & Hoeijmakers, J. G. J. (2024). Peripheral Pain Captured Centrally: Altered Brain Morphology on MRI in Small Fiber Neuropathy Patients With and Without an SCN9A Gene Variant. The Journal of Pain, 25(3), 730-741. https://doi.org/10.1016/j.jpain.2023.10.002

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., ... Evangelista, T. (2024). EURO-NMD registry: federated FAIR infrastructure, innovative technologies and concepts of a patient-centred registry for rare neuromuscular disorders. Orphanet Journal of Rare Diseases, 19(1), Article 66. https://doi.org/10.1186/s13023-024-03059-3