Works by Santens, Patrick


Results: 81
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    Parkinsonism due to lamotrigine.

    Published in:
    Movement Disorders, 2006, v. 21, n. 12, p. 2269, doi. 10.1002/mds.21125
    By:
    • Santens, Patrick;
    • Claeys, Isabel;
    • Vonck, Kristl;
    • Boon, Paul
    Publication type:
    Article
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    Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21.

    Published in:
    Nature, 2006, v. 442, n. 7105, p. 920, doi. 10.1038/nature05017
    By:
    • Cruts, Marc;
    • Gijselinck, Ilse;
    • van der Zee, Julie;
    • Engelborghs, Sebastiaan;
    • Wils, Hans;
    • Pirici, Daniel;
    • Rademakers, Rosa;
    • Vandenberghe, Rik;
    • Dermaut, Bart;
    • Martin, Jean-Jacques;
    • van Duijn, Cornelia;
    • Peeters, Karin;
    • Sciot, Raf;
    • Santens, Patrick;
    • De Pooter, Tim;
    • Mattheijssens, Maria;
    • Van den Broeck, Marleen;
    • Cuijt, Ivy;
    • Vennekens, Krist'l;
    • De Deyn, Peter P.
    Publication type:
    Article
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    Clinical Evidence of Disease Anticipation in Families Segregating a C9orf72 Repeat Expansion.

    Published in:
    JAMA Neurology, 2017, v. 74, n. 4, p. 445, doi. 10.1001/jamaneurol.2016.4847
    By:
    • Van Mossevelde, Sara;
    • van der Zee, Julie;
    • Gijselinck, Ilse;
    • Sleegers, Kristel;
    • De Bleecker, Jan;
    • Sieben, Anne;
    • Vandenberghe, Rik;
    • Van Langenhove, Tim;
    • Baets, Jonathan;
    • Deryck, Olivier;
    • Santens, Patrick;
    • Ivanoiu, Adrian;
    • Willems, Christiana;
    • Bäumer, Veerle;
    • Van den Broeck, Marleen;
    • Peeters, Karin;
    • Mattheijssens, Maria;
    • De Jonghe, Peter;
    • Cras, Patrick;
    • Martin, Jean-Jacques
    Publication type:
    Article
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    Gastric Helicobacter suis Infection Partially Protects against Neurotoxicity in A 6-OHDA Parkinson's Disease Mouse Model.

    Published in:
    International Journal of Molecular Sciences, 2021, v. 22, n. 21, p. 11328, doi. 10.3390/ijms222111328
    By:
    • Berlamont, Helena;
    • Bruggeman, Arnout;
    • Bauwens, Eva;
    • Vandendriessche, Charysse;
    • Clarebout, Elien;
    • Xie, Junhua;
    • De Bruyckere, Sofie;
    • Van Imschoot, Griet;
    • Van Wonterghem, Elien;
    • Ducatelle, Richard;
    • Santens, Patrick;
    • Smet, Annemieke;
    • Haesebrouck, Freddy;
    • Vandenbroucke, Roosmarijn E.
    Publication type:
    Article
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    Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brains.

    Published in:
    Acta Neuropathologica Communications, 2015, v. 3, p. 1, doi. 10.1186/s40478-015-0246-7
    By:
    • Janssens, Jonathan;
    • Philtjens, Stéphanie;
    • Kleinberger, Gernot;
    • Van Mossevelde, Sara;
    • van der Zee, Julie;
    • Cacace, Rita;
    • Engelborghs, Sebastiaan;
    • Sieben, Anne;
    • Banzhaf-Strathmann, Julia;
    • Dillen, Lubina;
    • Merlin, Céline;
    • Cuijt, Ivy;
    • Robberecht, Caroline;
    • Schmid, Bettina;
    • Santens, Patrick;
    • Ivanoiu, Adrian;
    • Vandenbulcke, Mathieu;
    • Vandenberghe, Rik;
    • Cras, Patrick;
    • De Deyn, Peter P.
    Publication type:
    Article
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    A Belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLD.

    Published in:
    Brain: A Journal of Neurology, 2006, v. 129, n. 4, p. 841, doi. 10.1093/brain/awl029
    By:
    • Julie van der Zee;
    • Rosa Rademakers;
    • Sebastiaan Engelborghs;
    • Ilse Gijselinck;
    • Veerle Bogaerts;
    • Rik Vandenberghe;
    • Patrick Santens;
    • Jo Caekebeke;
    • Tim De Pooter;
    • Karin Peeters;
    • Ursula Lübke;
    • Marleen Van den Broeck;
    • Jean-Jacques Martin;
    • Marc Cruts;
    • Peter P. De Deyn;
    • Christine Van Broeckhoven;
    • Bart Dermaut
    Publication type:
    Article
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    Mutations other than null mutations producing a pathogenic loss of progranulin in frontotemporal dementia.

    Published in:
    Human Mutation, 2007, v. 28, n. 4, p. 416, doi. 10.1002/humu.9484
    By:
    • van der Zee, Julie;
    • Le Ber, Isabelle;
    • Maurer-Stroh, Sebastian;
    • Engelborghs, Sebastiaan;
    • Gijselinck, Ilse;
    • Camuzat, Agnès;
    • Brouwers, Nathalie;
    • Vandenberghe, Rik;
    • Sleegers, Kristel;
    • Hannequin, Didier;
    • Dermaut, Bart;
    • Schymkowitz, Joost;
    • Campion, Dominique;
    • Santens, Patrick;
    • Martin, Jean-Jacques;
    • Lacomblez, Lucette;
    • De Pooter, Tim;
    • Peeters, Karin;
    • Mattheijssens, Maria;
    • Vercelletto, Martine
    Publication type:
    Article
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    The genetics and neuropathology of frontotemporal lobar degeneration.

    Published in:
    Acta Neuropathologica, 2012, v. 124, n. 3, p. 353, doi. 10.1007/s00401-012-1029-x
    By:
    • Sieben, Anne;
    • Van Langenhove, Tim;
    • Engelborghs, Sebastiaan;
    • Martin, Jean-Jacques;
    • Boon, Paul;
    • Cras, Patrick;
    • De Deyn, Peter-Paul;
    • Santens, Patrick;
    • Van Broeckhoven, Christine;
    • Cruts, Marc
    Publication type:
    Article
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    Extended FTLD pedigree segregating a Belgian <italic>GRN</italic>-null mutation: neuropathological heterogeneity in one family.

    Published in:
    Alzheimer's Research & Therapy, 2018, v. 10, p. 1, doi. 10.1186/s13195-017-0334-y
    By:
    • Sieben, Anne;
    • Van Mossevelde, Sara;
    • Wauters, Eline;
    • Engelborghs, Sebastiaan;
    • van der Zee, Julie;
    • Van Langenhove, Tim;
    • Santens, Patrick;
    • Praet, Marleen;
    • Boon, Paul;
    • Miatton, Marijke;
    • Van Hoecke, Sofie;
    • Vandenbulcke, Mathieu;
    • Vandenberghe, Rik;
    • Cras, Patrick;
    • Cruts, Marc;
    • De Deyn, Peter Paul;
    • Van Broeckhoven, Christine;
    • Martin, Jean-Jacques
    Publication type:
    Article