P.F. Sinnige

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  1. Imaging in cutis laxa syndrome caused by a dominant negative ALDH18A1 mutation, with hypotheses for intracranial vascular tortuosity and wide perivascular spaces

    Sinnige, P. F., van Rauenswaaij-Arts, C. M. A., Caruso, P., Lin, A. E., Boon, M., Rahikkala, E., Callewaert, B. & Meiners, L. C., Nov-2017, In : European Journal of Paediatric Neurology. 21, 6, p. 912-920 9 p.

    Research output: Contribution to journalArticleAcademicpeer-review

  2. Children with idiopathic tics reveal additional features of hyperkinetic movement disorders

    Sinnige, P. F., Brandsma, R., Eggink, W., Kuiper, M. J., Lunsing, I. J., Boon, M., Delnooz, C. C. S., van Egmond, M. E., Sinnige, O. G. F., de Vries, J. J., Hoekstra, P. J. & Sival, D. A., 21-Jun-2016, In : Movement Disorders. 31, p. S309-S309 1 p., 967.

    Research output: Contribution to journalMeeting AbstractAcademic

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ID: 25397915