Works matching IS 00068950 AND DT 2019 AND VI 142 AND IP 6

Results: 37
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    Network localization of cervical dystonia based on causal brain lesions.

    Published in:
    2019
    By:
    • Corp, Daniel T;
    • Joutsa, Juho;
    • Darby, R Ryan;
    • Delnooz, Cathérine C S;
    • Warrenburg, Bart P C van de;
    • Cooke, Danielle;
    • Prudente, Cecília N;
    • Ren, Jianxun;
    • Reich, Martin M;
    • Batla, Amit;
    • Bhatia, Kailash P;
    • Jinnah, Hyder A;
    • Liu, Hesheng;
    • Fox, Michael D;
    • van de Warrenburg, Bart P C
    Publication type:
    journal article
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    A multicentre longitudinal study of flortaucipir (18F) in normal ageing, mild cognitive impairment and Alzheimer's disease dementia.

    Published in:
    2019
    By:
    • Pontecorvo, Michael J;
    • Devous, Michael D;
    • Kennedy, Ian;
    • Navitsky, Michael;
    • Lu, Ming;
    • Galante, Nicholas;
    • Salloway, Stephen;
    • Doraiswamy, P Murali;
    • Southekal, Sudeepti;
    • Arora, Anupa K;
    • McGeehan, Anne;
    • Lim, Nathaniel C;
    • Xiong, Hui;
    • Truocchio, Stephen P;
    • Joshi, Abhinay D;
    • Shcherbinin, Sergey;
    • Teske, Brian;
    • Fleisher, Adam S;
    • Mintun, Mark A
    Publication type:
    journal article
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    Limbic-predominant age-related TDP-43 encephalopathy (LATE): consensus working group report.

    Published in:
    2019
    By:
    • Nelson, Peter T;
    • Dickson, Dennis W;
    • Trojanowski, John Q;
    • Jack, Clifford R;
    • Boyle, Patricia A;
    • Arfanakis, Konstantinos;
    • Rademakers, Rosa;
    • Alafuzoff, Irina;
    • Attems, Johannes;
    • Brayne, Carol;
    • Coyle-Gilchrist, Ian T S;
    • Chui, Helena C;
    • Fardo, David W;
    • Flanagan, Margaret E;
    • Halliday, Glenda;
    • Hokkanen, Suvi R K;
    • Hunter, Sally;
    • Jicha, Gregory A;
    • Katsumata, Yuriko;
    • Kawas, Claudia H
    Publication type:
    journal article
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    FAHN/SPG35: a narrow phenotypic spectrum across disease classifications.

    Published in:
    2019
    By:
    • Rattay, Tim W;
    • Lindig, Tobias;
    • Baets, Jonathan;
    • Smets, Katrien;
    • Deconinck, Tine;
    • Söhn, Anne S;
    • Hörtnagel, Konstanze;
    • Eckstein, Kathrin N;
    • Wiethoff, Sarah;
    • Reichbauer, Jennifer;
    • Döbler-Neumann, Marion;
    • Krägeloh-Mann, Ingeborg;
    • Auer-Grumbach, Michaela;
    • Plecko, Barbara;
    • Münchau, Alexander;
    • Wilken, Bernd;
    • Janauschek, Marc;
    • Giese, Anne-Katrin;
    • Bleecker, Jan L De;
    • Ortibus, Els
    Publication type:
    journal article
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    The expanded clinical spectrum of anti-GABABR encephalitis and added value of KCTD16 autoantibodies.

    Published in:
    2019
    By:
    • Coevorden-Hameete, Marleen H van;
    • Bruijn, Marienke A A M de;
    • Graaff, Esther de;
    • Bastiaansen, Danielle A E M;
    • Schreurs, Marco W J;
    • Demmers, Jeroen A A;
    • Ramberger, Melanie;
    • Hulsenboom, Esther S P;
    • Nagtzaam, Mariska M P;
    • Boukhrissi, Sanae;
    • Veldink, Jan H;
    • Verschuuren, Jan J G M;
    • Hoogenraad, Casper C;
    • Smitt, Peter A E Sillevis;
    • Titulaer, Maarten J;
    • van Coevorden-Hameete, Marleen H;
    • de Bruijn, Marienke A A M;
    • de Graaff, Esther;
    • Sillevis Smitt, Peter A E
    Publication type:
    journal article
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    Editorial.

    Published in:
    2019
    By:
    • Kullmann, Dimitri M
    Publication type:
    Editorial
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    Corrigendum.

    Published in:
    2019
    Publication type:
    journal article
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    Corrigendum.

    Published in:
    2019
    Publication type:
    journal article
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    Corrigendum.

    Published in:
    2019
    Publication type:
    journal article
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    Corrigendum.

    Published in:
    2019
    Publication type:
    journal article
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    Corrigendum.

    Published in:
    2019
    Publication type:
    journal article
    33

    Corrigendum.

    Published in:
    2019
    Publication type:
    journal article
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    The clinical spectrum of the congenital myasthenic syndrome resulting from COL13A1 mutations.

    Published in:
    2019
    By:
    • Cruz, Pedro M. Rodríguez;
    • Cossins, Judith;
    • Estephan, Eduardo de Paula;
    • Munell, Francina;
    • Selby, Kathryn;
    • Hirano, Michio;
    • Maroofin, Reza;
    • Mehrjardi, Mohammad Yahya Vahidi;
    • Chow, Gabriel;
    • Carr, Aisling;
    • Manzur, Adnan;
    • Robb, Stephanie;
    • Munot, Pinki;
    • Liu, Wei Wei;
    • Banka, Siddharth;
    • Fraser, Harry;
    • Goede, Christian De;
    • Zanoteli, Edmar;
    • Reed, Umbertina Conti;
    • Sage, Abigail
    Publication type:
    journal article
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    Biallelic MYORG mutation carriers exhibit primary brain calcification with a distinct phenotype.

    Published in:
    2019
    By:
    • Grangeon, Lou;
    • Wallon, David;
    • Charbonnier, Camille;
    • Quenez, Olivier;
    • Richard, Anne-Claire;
    • Rousseau, Stéphane;
    • Budowski, Clara;
    • Lebouvier, Thibaud;
    • Corbille, Anne-Gaëlle;
    • Vidailhet, Marie;
    • Méneret, Aurélie;
    • Roze, Emmanuel;
    • Anheim, Mathieu;
    • Tranchant, Christine;
    • Favrole, Pascal;
    • Antoine, Jean-Christophe;
    • Defebvre, Luc;
    • Ayrignac, Xavier;
    • Labauge, Pierre;
    • Pariente, Jérémie
    Publication type:
    journal article
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