Works matching IS 00068950 AND DT 2020 AND VI 143 AND IP 10

Results: 36
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    A novel RFC1 repeat motif (ACAGG) in two Asia-Pacific CANVAS families.

    Published in:
    2020
    By:
    • Scriba, Carolin K;
    • Beecroft, Sarah J;
    • Clayton, Joshua S;
    • Cortese, Andrea;
    • Sullivan, Roisin;
    • Yau, Wai Yan;
    • Dominik, Natalia;
    • Rodrigues, Miriam;
    • Walker, Elizabeth;
    • Dyer, Zoe;
    • Wu, Teddy Y;
    • Davis, Mark R;
    • Chandler, David C;
    • Weisburd, Ben;
    • Houlden, Henry;
    • Reilly, Mary M;
    • Laing, Nigel G;
    • Lamont, Phillipa J;
    • Roxburgh, Richard H;
    • Ravenscroft, Gianina
    Publication type:
    journal article
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    Defining the clinical, molecular and imaging spectrum of adaptor protein complex 4-associated hereditary spastic paraplegia.

    Published in:
    2020
    By:
    • Ebrahimi-Fakhari, Darius;
    • Teinert, Julian;
    • Behne, Robert;
    • Wimmer, Miriam;
    • D'Amore, Angelica;
    • Eberhardt, Kathrin;
    • Brechmann, Barbara;
    • Ziegler, Marvin;
    • Jensen, Dana M;
    • Nagabhyrava, Premsai;
    • Geisel, Gregory;
    • Carmody, Erin;
    • Shamshad, Uzma;
    • Dies, Kira A.;
    • Yuskaitis, Christopher J;
    • Salussolia, Catherine L;
    • Ebrahimi-Fakhari, Daniel;
    • Pearson, Toni S;
    • Saffari, Afshin;
    • Ziegler, Andreas
    Publication type:
    journal article
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    Editorial.

    Published in:
    2020
    By:
    • Kullmann, Dimitri M
    Publication type:
    Editorial
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    Predicting future rates of tau accumulation on PET.

    Published in:
    2020
    By:
    • Jack, Clifford R;
    • Wiste, Heather J;
    • Weigand, Stephen D;
    • Therneau, Terry M;
    • Lowe, Val J;
    • Knopman, David S;
    • Botha, Hugo;
    • Graff-Radford, Jonathan;
    • Jones, David T;
    • Ferman, Tanis J;
    • Boeve, Bradley F;
    • Kantarci, Kejal;
    • Vemuri, Prashanthi;
    • Mielke, Michelle M;
    • Whitwell, Jennifer;
    • Josephs, Keith;
    • Schwarz, Christopher G;
    • Senjem, Matthew L;
    • Gunter, Jeffrey L;
    • Petersen, Ronald C
    Publication type:
    journal article
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    Disease-modifying drugs can reduce disability progression in relapsing multiple sclerosis.

    Published in:
    2020
    By:
    • Amato, Maria Pia;
    • Fonderico, Mattia;
    • Portaccio, Emilio;
    • Pastò, Luisa;
    • Razzolini, Lorenzo;
    • Prestipino, Elio;
    • Bellinvia, Angelo;
    • Tudisco, Laura;
    • Fratangelo, Roberto;
    • Comi, Giancarlo;
    • Patti, Francesco;
    • Luca, Giovanna De;
    • Morra, Vincenzo Brescia;
    • Cocco, Eleonora;
    • Pozzilli, Carlo;
    • Sola, Patrizia;
    • Bergamaschi, Roberto;
    • Salemi, Giuseppe;
    • Inglese, Matilde;
    • Millefiorini, Enrico
    Publication type:
    journal article
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    The emerging spectrum of COVID-19 neurology: clinical, radiological and laboratory findings.

    Published in:
    2020
    By:
    • Paterson, Ross W;
    • Brown, Rachel L;
    • Benjamin, Laura;
    • Nortley, Ross;
    • Wiethoff, Sarah;
    • Bharucha, Tehmina;
    • Jayaseelan, Dipa L;
    • Kumar, Guru;
    • Raftopoulos, Rhian E;
    • Zambreanu, Laura;
    • Vivekanandam, Vinojini;
    • Khoo, Anthony;
    • Geraldes, Ruth;
    • Chinthapalli, Krishna;
    • Boyd, Elena;
    • Tuzlali, Hatice;
    • Price, Gary;
    • Christofi, Gerry;
    • Morrow, Jasper;
    • McNamara, Patricia
    Publication type:
    journal article
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    Mitochondrial damage-associated inflammation highlights biomarkers in PRKN/PINK1 parkinsonism.

    Published in:
    2020
    By:
    • Borsche, Max;
    • König, Inke R;
    • Delcambre, Sylvie;
    • Petrucci, Simona;
    • Balck, Alexander;
    • Brüggemann, Norbert;
    • Zimprich, Alexander;
    • Wasner, Kobi;
    • Pereira, Sandro L;
    • Avenali, Micol;
    • Deuschle, Christian;
    • Badanjak, Katja;
    • Ghelfi, Jenny;
    • Gasser, Thomas;
    • Kasten, Meike;
    • Rosenstiel, Philip;
    • Lohmann, Katja;
    • Brockmann, Kathrin;
    • Valente, Enza Maria;
    • Youle, Richard J
    Publication type:
    journal article
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    YIF1B mutations cause a post-natal neurodevelopmental syndrome associated with Golgi and primary cilium alterations.

    Published in:
    2020
    By:
    • Diaz, Jorge;
    • Gérard, Xavier;
    • Emerit, Michel-Boris;
    • Areias, Julie;
    • Geny, David;
    • Dégardin, Julie;
    • Simonutti, Manuel;
    • Guerquin, Marie-Justine;
    • Collin, Thibault;
    • Viollet, Cécile;
    • Billard, Jean-Marie;
    • Métin, Christine;
    • Hubert, Laurence;
    • Larti, Farzaneh;
    • Kahrizi, Kimia;
    • Jobling, Rebekah;
    • Agolini, Emanuele;
    • Shaheen, Ranad;
    • Zigler, Alban;
    • Rouiller-Fabre, Virginie
    Publication type:
    journal article
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    Functional cognitive disorder: dementia's blind spot.

    Published in:
    2020
    By:
    • Ball, Harriet A;
    • McWhirter, Laura;
    • Ballard, Clive;
    • Bhome, Rohan;
    • Blackburn, Daniel J;
    • Edwards, Mark J;
    • Fleming, Stephen M;
    • Fox, Nick C;
    • Howard, Robert;
    • Huntley, Jonathan;
    • Isaacs, Jeremy D;
    • Larner, Andrew J;
    • Nicholson, Timothy R;
    • Pennington, Catherine M;
    • Poole, Norman;
    • Price, Gary;
    • Price, Jason P;
    • Reuber, Markus;
    • Ritchie, Craig;
    • Rossor, Martin N
    Publication type:
    journal article
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