I.B.T. Joosten

Recente publicaties

• Vosse, B. A. H., Horlings, C. G. C., Joosten, I. B. T., Cobben, N. A. M., van Kuijk, S. M. J., Wijkstra, P. J., & Faber, C. G. (2023). Role of respiratory characteristics in treatment adherence with noninvasive home mechanical ventilation in myotonic dystrophy type 1, a retrospective study. Neuromuscular Disorders, 33(9), 57-62. https://doi.org/10.1016/j.nmd.2023.08.004

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• Joosten, I. B. T., Janssen, C. E. W., Horlings, C. G. C., den Uijl, D., Evertz, R., van Engelen, B. G. M., Faber, C. G., & Vernooy, K. (2023). An evaluation of 24 h Holter monitoring in patients with myotonic dystrophy type 1. EP Europace, 25(1), 156-163. https://doi.org/10.1093/europace/euac104

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• Joosten, I. B. T., Horlings, C. G. C., Vosse, B. A. H., Wagner, A., Bovenkerk, D. S. H., Evertz, R., Vernooy, K., van Engelen, B. G. M., & Faber, C. G. (2023). Myotonic dystrophy type 1: a comparison between the adult- and late-onset subtype. Muscle & Nerve, 67(2), 130-137. https://doi.org/10.1002/mus.27766

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• Joosten, I. B. T., Fuchs, C. J., Beelen, M., Plasqui, G., Van Loon, L. J. C., & Faber, C. G. (2023). Energy Expenditure, Body Composition, and Skeletal Muscle Oxidative Capacity in Patients with Myotonic Dystrophy Type 1. Journal of neuromuscular diseases, 10(4), 701-712. https://doi.org/10.3233/JND-230036

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• Joosten, I. B. T. (2023). Myotonic dystrophy type 1: clinical genetics and multisystem involvement. [Doctoral Thesis, Maastricht University]. Maastricht University. https://doi.org/10.26481/dis.20231023ij

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• Sopacua, M., Gorissen-Brouwers, C. M. L., de Greef, B. T. A., Joosten, I. B. T., Faber, C. G., Merkies, I. S. J., & Hoeijmakers, J. G. J. (2022). The applicability of the digit wrinkle scan to quantify sympathetic nerve function. Clinical Neurophysiology Practice, 7, 115-119. https://doi.org/10.1016/j.cnp.2022.03.005

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• Joosten, I. B. T., van Lohuizen, R., den Uijl, D. W., Evertz, R., de Greef, B. T. A., van Engelen, B. G. M., Faber, C. G., & Vernooy, K. (2021). Electrocardiographic predictors of infrahissian conduction disturbances in myotonic dystrophy type 1. EP Europace, 23(2), 298-304. https://doi.org/10.1093/europace/euaa256

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• Joosten, I. B. T., Hellebrekers, D. M. E. I., de Greef, B. T. A., Smeets, H. J. M., de Die-Smulders, C. E. M., Faber, C. G., & Gerrits, M. M. (2020). Parental repeat length instability in myotonic dystrophy type 1 pre- and protomutations. European Journal of Human Genetics, 28(7), 956-962. https://doi.org/10.1038/s41431-020-0601-4

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• Joosten, I. B. T., & Hoeijmakers, J. G. J. (2018). Mystery Case: Superior oblique myokymia: An uncommon cause of intermittent diplopia. Neurology, 90(9), E814-E814. https://doi.org/10.1212/WNL.0000000000005028

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