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Fingerprint Dive into the research topics where A.J. Rozemuller is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

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Research Output

Amyloid-beta and phosphorylated tau in post-mortem Alzheimer's disease retinas

den Haan, J., Morrema, T. H. J., Verbraak, F. D., de Boer, J. F., Scheltens, P., Rozemuller, A. J., Bergen, A. A. B., Bouwman, F. H. & Hoozemans, J. J., Oct 2018, In : Acta neuropathologica communications. 6, 1, p. 147

Research output: Contribution to journal/periodicalArticleScientificpeer-review

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    LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing study

    Quadri, M., Mandemakers, W., Grochowska, M. M., Masius, R., Geut, H., Fabrizio, E., Breedveld, G. J., Kuipers, D., Minneboo, M., Vergouw, L. J. M., Carreras Mascaro, A., Yonova-Doing, E., Simons, E., Zhao, T., Di Fonzo, A. B., Chang, H-C., Parchi, P., Melis, M., Correia Guedes, L., Criscuolo, C. & 30 others, Thomas, A., Brouwer, R. W. W., Heijsman, D., Ingrassia, A. M. T., Calandra Buonaura, G., Rood, J. P., Capellari, S., Rozemuller, A. J., Sarchioto, M., Fen Chien, H., Vanacore, N., Olgiati, S., Wu-Chou, Y-H., Yeh, T-H., Boon, A. J. W., Hoogers, S. E., Ghazvini, M., IJpma, A. S., van IJcken, W. F. J., Onofrj, M., Barone, P., Nicholl, D. J., Puschmann, A., De Mari, M., Kievit, A. J., Barbosa, E., De Michele, G., Majoor-Krakauer, D., van Swieten, J. C. & de Jong, F. J., 2018, In : The Lancet Neurology. 17, p. 597-608

    Research output: Contribution to journal/periodicalArticleScientificpeer-review

  • Distribution and Load of Amyloid-β Pathology in Parkinson Disease and Dementia with Lewy Bodies

    Hepp, D. H., Vergoossen, D. L. E., Huisman, E., Lemstra, A. W., Berendse, H. W., Rozemuller, A. J., Foncke, E. M. J. & van de Berg, W. D. J., 2016, In : Journal of Neuropathology and Experimental Neurology. 75, p. 936-945

    Research output: Contribution to journal/periodicalArticleScientificpeer-review

    Open Access
  • PRKAR1B mutation associated with a new neurodegenerative disorder with unique pathology

    Wong, T. H., Chiu, W. Z., Breedveld, G. J., Li, K. W., Verkerk, A. J. M. H., Hondius, D., Hukema, R. K., Seelaar, H., Frick, P., Severijnen, L-A., Lammers, G-J., Lebbink, J. H. G., van Duinen, S. G., Kamphorst, W., Rozemuller, A. J., Bakker, E. B., Neumann, M., Willemsen, R., Bonifati, V., Smit, A. B. & 1 others, van Swieten, J., 2014, In : Brain: a journal of neurology. 137, Pt 5, p. 1361-73 13 p.

    Research output: Contribution to journal/periodicalArticleScientificpeer-review

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    A second class of Gerstmann-Straussler-Scheinker disease linked to the G131V mutation in the prion protein gene in a Dutch patient.

    Jansen, C., Parchi, P., Capellari, S., Stramiello, R., Dopper, E. G., Van Swieten, J. C., Kamphorst, W. & Rozemuller, A. J., 2011, In : Journal of Neuropathology and Experimental Neurology. 70, p. 698-702

    Research output: Contribution to journal/periodicalArticleScientificpeer-review