Works matching IS 03645134 AND DT 2016 AND VI 79 AND IP 6

Results: 21
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    White matter hyperintensities are a core feature of Alzheimer's disease: Evidence from the dominantly inherited Alzheimer network.

    Published in:
    2016
    By:
    • Lee, Seonjoo;
    • Viqar, Fawad;
    • Zimmerman, Molly E.;
    • Narkhede, Atul;
    • Tosto, Giuseppe;
    • Benzinger, Tammie L.S.;
    • Marcus, Daniel S.;
    • Fagan, Anne M.;
    • Goate, Alison;
    • Fox, Nick C.;
    • Cairns, Nigel J.;
    • Holtzman, David M.;
    • Buckles, Virginia;
    • Ghetti, Bernardino;
    • McDade, Eric;
    • Martins, Ralph N.;
    • Saykin, Andrew J.;
    • Masters, Colin L.;
    • Ringman, John M.;
    • Ryan, Natalie S.
    Publication type:
    journal article
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    Whole exome sequencing in patients with white matter abnormalities.

    Published in:
    2016
    By:
    • Vanderver, Adeline;
    • Simons, Cas;
    • Helman, Guy;
    • Crawford, Joanna;
    • Wolf, Nicole I.;
    • Bernard, Geneviève;
    • Pizzino, Amy;
    • Schmidt, Johanna L.;
    • Takanohashi, Asako;
    • Miller, David;
    • Khouzam, Amirah;
    • Rajan, Vani;
    • Ramos, Erica;
    • Chowdhury, Shimul;
    • Hambuch, Tina;
    • Ru, Kelin;
    • Baillie, Gregory J.;
    • Grimmond, Sean M.;
    • Caldovic, Ljubica;
    • Devaney, Joseph
    Publication type:
    journal article
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    DNA repair pathways underlie a common genetic mechanism modulating onset in polyglutamine diseases.

    Published in:
    2016
    By:
    • Bettencourt, Conceição;
    • Hensman‐Moss, Davina;
    • Flower, Michael;
    • Wiethoff, Sarah;
    • Brice, Alexis;
    • Goizet, Cyril;
    • Stevanin, Giovanni;
    • Koutsis, Georgios;
    • Karadima, Georgia;
    • Panas, Marios;
    • Yescas‐Gómez, Petra;
    • García‐Velázquez, Lizbeth Esmeralda;
    • Alonso‐Vilatela, María Elisa;
    • Lima, Manuela;
    • Raposo, Mafalda;
    • Traynor, Bryan;
    • Sweeney, Mary;
    • Wood, Nicholas;
    • Giunti, Paola;
    • Durr, Alexandra
    Publication type:
    journal article
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    α-synuclein genetic variability: A biomarker for dementia in Parkinson disease.

    Published in:
    2016
    By:
    • Guella, Ilaria;
    • Evans, Daniel M.;
    • Szu‐Tu, Chelsea;
    • Nosova, Ekaterina;
    • Bortnick, Stephanie F.;
    • Goldman, Jennifer G.;
    • Dalrymple‐Alford, John C.;
    • Geurtsen, Gert J.;
    • Litvan, Irene;
    • Ross, Owen A.;
    • Middleton, Lefkos T.;
    • Parkkinen, Laura;
    • Farrer, Matthew J.;
    • Szu-Tu, Chelsea;
    • SNCA Cognition Study Group;
    • Dalrymple-Alford, John C
    Publication type:
    journal article
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    Targeting coagulation factor XII as a novel therapeutic option in brain trauma.

    Published in:
    2016
    By:
    • Hopp, Sarah;
    • Albert‐Weissenberger, Christiane;
    • Mencl, Stine;
    • Bieber, Michael;
    • Schuhmann, Michael K.;
    • Stetter, Christian;
    • Nieswandt, Bernhard;
    • Schmidt, Peter M.;
    • Monoranu, Camelia‐Maria;
    • Alafuzoff, Irina;
    • Marklund, Niklas;
    • Nolte, Marc W.;
    • Sirén, Anna‐Leena;
    • Kleinschnitz, Christoph
    Publication type:
    journal article
    17

    Mutation-specific effects on thin filament length in thin filament myopathy.

    Published in:
    2016
    By:
    • Winter, Josine M. de;
    • Joureau, Barbara;
    • Lee, Eun‐Jeong;
    • Kiss, Balázs;
    • Yuen, Michaela;
    • Gupta, Vandana A.;
    • Pappas, Christopher T.;
    • Gregorio, Carol C.;
    • Stienen, Ger J. M.;
    • Edvardson, Simon;
    • Wallgren‐Pettersson, Carina;
    • Lehtokari, Vilma‐Lotta;
    • Pelin, Katarina;
    • Malfatti, Edoardo;
    • Romero, Norma B.;
    • Engelen, Baziel G. van;
    • Voermans, Nicol C.;
    • Donkervoort, Sandra;
    • Bönnemann, C. G.;
    • Clarke, Nigel F.
    Publication type:
    journal article
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