M. Oosterloo

Considine, C. M., Eddy, C. M., Frank, S. A., Kostyk, S. K., Oosterloo, M., Killoran, A., Furr Stimming, E., Dose, M., Cruickshank, T., Bird, T. D., Vetter, L., Arnesen, A., Valvano, J., Lange, H. W., & Claassen, D. O. (2025). Improving the Clinical Diagnostic Criteria for Genetically Confirmed Adult-Onset Huntington Disease. Neurology: Clinical Practice, 15(2), Article e200427. https://doi.org/10.1212/CPJ.0000000000200427

Daemen, M. M. J., De Bruijn-Heijligers, B. A. A. G., Van Der Heijden, C., Boots, L. M. M., Oosterloo, M., De Vugt, M. E., & Duits, A. A. (2025). Navigating Life With Parkinson's Disease: A Focus Group Study on Coping Strategies and Considerations for Self-Management Support. Journal of Advanced Nursing, 81(4), 2003-2012. https://doi.org/10.1111/jan.16414

Daemen, M. M., Duits, A. A., van der Meer, L. B., Andriessen, R. L., Veenhuizen, R. B., Wassenberg, R., Peeters, T., de Jager, L., & Oosterloo, M. (2025). Through their eyes: A retrospective mixed-methods study on the experiences and support needs of children growing up with a parent with Huntington's disease. Journal of Huntington's disease, 14(1), 93-102. https://doi.org/10.1177/18796397241304333

Andriessen, R. L., Oosterloo, M., Molema, J., Daemen, M. M. J., Linden, D. E. J., & Leentjens, A. F. G. (2025). Pharmacological Treatment of Neuropsychiatric Symptoms in Huntington's Disease: A Systematic Review. Movement Disorders Clinical Practice. Advance online publication. https://doi.org/10.1002/mdc3.14343

Daemen, M. M. J., Boots, L. M. M., Oosterloo, M., de Vugt, M. E., & Duits, A. A. (2024). Evaluating the web-based 'Partner in Balance' program for informal caregivers of people with Huntington's disease: A pilot study. Internet Interventions, 38, Article 100782. https://doi.org/10.1016/j.invent.2024.100782

Heffels, J. C. F., Oosterloo, M., de Boer, B., Roos, R. A. C., Schols, J. M. G. A., & Everink, I. H. J. (2024). Quality of care through the eyes of residents with Huntington's disease living in a nursing home: A qualitative explorative study. Journal of Huntington's disease, 13(4), 523-533. https://doi.org/10.1177/18796397241289374

van Os, N. J. H., Oosterloo, M., Grutters, J. P. C., Essers, B. A. B., & van de Warrenburg, B. P. C. (2024). Preferences for genetic interventions for SCA and Huntington's disease: results of a discrete choice experiment among patients. Orphanet Journal of Rare Diseases, 19(1), Article 398. https://doi.org/10.1186/s13023-024-03408-2

van Os, N. J. H., Oosterloo, M., Essers, B. A. B., Grutters, J. P. C., & van de Warrenburg, B. P. C. (2024). Genetic Interventions for Spinocerebellar Ataxia and Huntington's Disease: A Qualitative Study of the Patient Perspective. Journal of Huntington's disease, 13(3), 321-328. https://doi.org/10.3233/JHD-240026

van Prooije, T. H., Pennings, M., Dorresteijn, L., Gardeitchik, T., Odekerken, V. J. J., Oosterloo, M., Pedersen, A., Verschuuren-Bemelmans, C. C., Vrancken, A., Kamsteeg, E. J., & van de Warrenburg, B. P. C. (2024). A New Case Series Suggests That SCA48 (ATX/STUB1) Is Primarily a Monogenic Disorder. Movement Disorders, 39(9), 1636-1640. https://doi.org/10.1002/mds.29912

Oosterloo, M., Touze, A., Byrne, L. M., Achenbach, J., Aksoy, H., Coleman, A., Lammert, D., Nance, M., Nopoulos, P., Reilmann, R., Saft, C., Santini, H., Squitieri, F., Tabrizi, S., Burgunder, J.-M., Quarrell, O., & Pediatric Huntington Disease Working Group of the European Huntington Disease Network (2024). Clinical Review of Juvenile Huntington's Disease. Journal of Huntington's disease, (1). Advance online publication. https://doi.org/10.3233/JHD-231523