Research output per year
Research output per year
Personal profile
specialisation
Rare genetic and congenital neurodevelopmental disorders
Research interests
Interventions in rare genetic neurodevelopmental disorders and inborn errors of metabolism by developing an n-of-1 methodology.
Collaborations and top research areas from the last five years
Recent external collaboration on country/territory level. Dive into details by clicking on the dots or
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Accessibility and feasibility of experience sampling methods for mental health research with people with intellectual disability: Scoping of research and stakeholder views: Scoping of research and stakeholder views
Bakkum, L., Paalman, C., Müller, A., Eeghen, A. V. & Schuengel, C., Jan 2024, In: JOURNAL OF APPLIED RESEARCH IN INTELLECTUAL DISABILITIES. 37, 2, e13190.Research output: Contribution to journal › Article › Academic › peer-review
Open Access -
Breaking the chains of lipoprotein lipase deficiency: A pediatric perspective on the efficacy and safety of Volanesorsen
den Hollander, B., Brands, M. M., Nijhuis, I. J. M., Doude van Troostwijk, L. J. A. E., van Essen, P., Hofsteenge, A. H., Koot, B. G., Müller, A. R., Tseng, L. A., Stroes, E. S. G., van de Ven, P. M., Wiegman, A. & van Karnebeek, C. D. M., May 2024, In: Molecular Genetics and Metabolism. 142, 1, p. 108347 108347.Research output: Contribution to journal › Article › Academic › peer-review
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Cannabidiol (Epidyolex®) for severe behavioral manifestations in patients with tuberous sclerosis complex, mucopolysaccharidosis type III and fragile X syndrome: protocol for a series of randomized, placebo-controlled N-of-1 trials
Müller, A. R., den Hollander, B., van de Ven, P. M., Roes, K. C. B., Geertjens, L., Bruining, H., van Karnebeek, C. D. M., Jansen, F. E., de Wit, M. C. Y., Ten Hoopen, L. W., Rietman, A. B., Dierckx, B., Wijburg, F. A., Boot, E., Brands, M. M. G. & van Eeghen, A. M., 1 Dec 2024, In: BMC psychiatry. 24, 1, p. 23 23.Research output: Contribution to journal › Article › Academic › peer-review
Open Access -
Correction: Understanding the impact of tuberous sclerosis complex: development and validation of the TSC-PROM (BMC Medicine, (2023), 21, 1, (298), 10.1186/s12916-023-03012-4)
Müller, A. R., Luijten, M. A. J., Haverman, L., de Ranitz-Greven, W. L., Janssens, P., Rietman, A. B., Hoopen, L. W. T., de Graaff, L. C. G., de Wit, M-C., Jansen, A. C., Gipson, T., Capal, J. K., de Vries, P. J. & van Eeghen, A. M., 1 Dec 2023, In: BMC medicine. 21, 1, 401.Research output: Contribution to journal › Comment/Letter to the editor › Academic
Open Access -
Parkinsonism in Genetic Neurodevelopmental Disorders: A Systematic Review
von Scheibler, E. N. M. M., van Eeghen, A. M., de Koning, T. J., Kuijf, M. L., Zinkstok, J. R., Müller, A. R., van Amelsvoort, T. A. M. J. & Boot, E., Jan 2023, In: Movement Disorders Clinical Practice. 10, 1, p. 17-31 15 p.Research output: Contribution to journal › Review article › Academic › peer-review
Open Access3 Citations (Scopus)