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Pontocerebellar hypoplasia due to bi-allelic variants in MINPP1
Appelhof, B., Wagner, M., Hoefele, J., Heinze, A., Roser, T., Koch-Hogrebe, M., Roosendaal, S. D., Dehghani, M., Mehrjardi, M. Y. V., Torti, E., Houlden, H., Maroofian, R., Rajabi, F., Sticht, H., Baas, F., Wieczorek, D. & Jamra, R. A., Mar 2021, In: European journal of human genetics. 29, 3, p. 411-421 11 p.Research output: Contribution to journal › Article › Academic › peer-review
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Effects on staff outcomes from an intervention for management of neuropsychiatric symptoms in residents of young-onset dementia care units: A cluster randomised controlled trial
van Duinen-van den IJssel, J. C. L., Bakker, C., Smalbrugge, M., Zwijsen, S. A., Appelhof, B., Teerenstra, S., Zuidema, S. U., de Vugt, M. E., Verhey, F. R. J. & Koopmans, R. T. C. M., 1 Aug 2019, In: International journal of nursing studies. 96, p. 35-43Research output: Contribution to journal › Article › Academic › peer-review
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A de novo missense mutation in the inositol 1,4,5-triphosphate receptor type 1 gene causing severe pontine and cerebellar hypoplasia: Expanding the phenotype of ITPR1-related spinocerebellar ataxia's
van Dijk, T., Barth, P., Reneman, L., Appelhof, B., Baas, F. & Poll-The, B. T., 2017, In: American Journal of Medical Genetics. Part A. 173A, 1, p. 207-212Research output: Contribution to journal › Article › Academic › peer-review
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