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Developmental neurobiology of cerebellar and Basal Ganglia connections.
Sival DA, Noort SAMV, Tijssen MAJ, de Koning TJ, Verbeek DS. Sival DA, et al. Among authors: tijssen maj. Eur J Paediatr Neurol. 2022 Jan;36:123-129. doi: 10.1016/j.ejpn.2021.12.001. Epub 2021 Dec 7. Eur J Paediatr Neurol. 2022. PMID: 34954622 Free article. Review.
Clinical, neuroradiological and genetic findings in pontocerebellar hypoplasia.
Namavar Y, Barth PG, Kasher PR, van Ruissen F, Brockmann K, Bernert G, Writzl K, Ventura K, Cheng EY, Ferriero DM, Basel-Vanagaite L, Eggens VR, Krägeloh-Mann I, De Meirleir L, King M, Graham JM Jr, von Moers A, Knoers N, Sztriha L, Korinthenberg R; PCH Consortium; Dobyns WB, Baas F, Poll-The BT. Namavar Y, et al. Brain. 2011 Jan;134(Pt 1):143-56. doi: 10.1093/brain/awq287. Epub 2010 Oct 15. Brain. 2011. PMID: 20952379 Free PMC article.
Functional MRI study of response inhibition in myoclonus dystonia.
van der Salm SM, van der Meer JN, Nederveen AJ, Veltman DJ, van Rootselaar AF, Tijssen MA. van der Salm SM, et al. Exp Neurol. 2013 Sep;247:623-9. doi: 10.1016/j.expneurol.2013.02.017. Epub 2013 Mar 6. Exp Neurol. 2013. PMID: 23474191
Assessment of speech in early-onset ataxia: a pilot study.
Kuiper MJ, Brandsma R, Lawerman TF, Lunsing RJ, Keegstra AL, Burger H, De Koning TJ, Tijssen MAJ, Sival DA. Kuiper MJ, et al. Among authors: tijssen maj. Dev Med Child Neurol. 2014 Dec;56(12):1202-1206. doi: 10.1111/dmcn.12517. Epub 2014 Jun 18. Dev Med Child Neurol. 2014. PMID: 24942085 Free article.
CACNA1B mutation is linked to unique myoclonus-dystonia syndrome.
Groen JL, Andrade A, Ritz K, Jalalzadeh H, Haagmans M, Bradley TE, Jongejan A, Verbeek DS, Nürnberg P, Denome S, Hennekam RC, Lipscombe D, Baas F, Tijssen MA. Groen JL, et al. Hum Mol Genet. 2015 Feb 15;24(4):987-93. doi: 10.1093/hmg/ddu513. Epub 2014 Oct 8. Hum Mol Genet. 2015. PMID: 25296916 Free PMC article.
353 results