Found: 5

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  • Aquaporin-4 and GPRC5B: old and new players in controlling brain oedema.

    Published in:
    Brain: A Journal of Neurology, 2023, v. 146, n. 8, p. 3444, doi. 10.1093/brain/awad146
    By:
    • Passchier, Emma M J;
    • Kerst, Sven;
    • Brouwers, Eelke;
    • Hamilton, Eline M C;
    • Bisseling, Quinty;
    • Bugiani, Marianna;
    • Waisfisz, Quinten;
    • Kitchen, Philip;
    • Unger, Lucas;
    • Breur, Marjolein;
    • Hoogterp, Leoni;
    • Vries, Sharon I de;
    • Abbink, Truus E M;
    • Kole, Maarten H P;
    • Leurs, Rob;
    • Vischer, Henry F;
    • Brignone, Maria S;
    • Ambrosini, Elena;
    • Feillet, François;
    • Born, Alfred P
    Publication type:
    Article

  • Complement-associated loss of CA2 inhibitory synapses in the demyelinated hippocampus impairs memory.

    Published in:
    Acta Neuropathologica, 2021, v. 142, n. 4, p. 643, doi. 10.1007/s00401-021-02338-8
    By:
    • Ramaglia, Valeria;
    • Dubey, Mohit;
    • Malpede, M. Alfonso;
    • Petersen, Naomi;
    • de Vries, Sharon I.;
    • Ahmed, Shanzeh M.;
    • Lee, Dennis S. W.;
    • Schenk, Geert J.;
    • Gold, Stefan M.;
    • Huitinga, Inge;
    • Gommerman, Jennifer L.;
    • Geurts, Jeroen J. G.;
    • Kole, Maarten H. P.
    Publication type:
    Article

  • Metachromatic leukodystrophy and transplantation: remyelination, no cross‐correction.

    Published in:
    Annals of Clinical & Translational Neurology, 2020, v. 7, n. 2, p. 169, doi. 10.1002/acn3.50975
    By:
    • Wolf, Nicole I.;
    • Breur, Marjolein;
    • Plug, Bonnie;
    • Beerepoot, Shanice;
    • Westerveld, Aimee S. R.;
    • van Rappard, Diane F.;
    • de Vries, Sharon I.;
    • Kole, Maarten H. P.;
    • Vanderver, Adeline;
    • van der Knaap, Marjo S.;
    • Lindemans, Caroline A.;
    • van Hasselt, Peter M.;
    • Boelens, Jaap J.;
    • Matzner, Ulrich;
    • Gieselmann, Volkmar;
    • Bugiani, Marianna
    Publication type:
    Article

  • Loss of CRB2 in Müller glial cells modifies a CRB1-associated retinitis pigmentosa phenotype into a Leber congenital amaurosis phenotype.

    Published in:
    Human Molecular Genetics, 2019, v. 28, n. 1, p. 105, doi. 10.1093/hmg/ddy337
    By:
    • Quinn, Peter M;
    • Mulder, Aat A;
    • Alves, C Henrique;
    • Desrosiers, Mélissa;
    • Vries, Sharon I de;
    • Klooster, Jan;
    • Dalkara, Deniz;
    • Koster, Abraham J;
    • Jost, Carolina R;
    • Wijnholds, Jan
    Publication type:
    Article

  • Axonal abnormalities in vanishing white matter.

    Published in:
    Annals of Clinical & Translational Neurology, 2018, v. 5, n. 4, p. 429, doi. 10.1002/acn3.540
    By:
    • Klok, Melanie D.;
    • Bugiani, Marianna;
    • de Vries, Sharon I.;
    • Gerritsen, Wouter;
    • Breur, Marjolein;
    • van der Sluis, Sophie;
    • Heine, Vivi M.;
    • Kole, Maarten H. P.;
    • Baron, Wia;
    • van der Knaap, Marjo S.
    Publication type:
    Article