Works by van Prooije, Teije H.


Results: 4
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    A New Case Series Suggests That SCA48 (ATX/STUB1) Is Primarily a Monogenic Disorder.

    Published in:
    Movement Disorders, 2024, v. 39, n. 9, p. 1636, doi. 10.1002/mds.29912
    By:
    • van Prooije, Teije H.;
    • Pennings, Maartje;
    • Dorresteijn, Lucille;
    • Gardeitchik, Thatjana;
    • Odekerken, Vincent J.J.;
    • Oosterloo, Mayke;
    • Pedersen, Annie;
    • Verschuuren‐Bemelmans, Corien C.;
    • Vrancken, Alexander;
    • Kamsteeg, Erik‐Jan;
    • van de Warrenburg, Bart P.C.
    Publication type:
    Article
    4

    The complexities of CACNA1A in clinical neurogenetics.

    Published in:
    Journal of Neurology, 2022, v. 269, n. 6, p. 3094, doi. 10.1007/s00415-021-10897-9
    By:
    • Hommersom, Marina P.;
    • van Prooije, Teije H.;
    • Pennings, Maartje;
    • Schouten, Meyke I.;
    • van Bokhoven, Hans;
    • Kamsteeg, Erik-Jan;
    • van de Warrenburg, Bart P. C.
    Publication type:
    Article