Works matching IS 03645134 AND DT 2017 AND VI 81 AND IP 3


Results: 23
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    Genetic variation at 16q24.2 is associated with small vessel stroke.

    Published in:
    2017
    By:
    • Traylor, Matthew;
    • Malik, Rainer;
    • Nalls, Mike A.;
    • Cotlarciuc, Ioana;
    • Radmanesh, Farid;
    • Thorleifsson, Gudmar;
    • Hanscombe, Ken B.;
    • Langefeld, Carl;
    • Saleheen, Danish;
    • Rost, Natalia S.;
    • Yet, Idil;
    • Spector, Tim D.;
    • Bell, Jordana T.;
    • Hannon, Eilis;
    • Mill, Jonathan;
    • Chauhan, Ganesh;
    • Debette, Stephanie;
    • Bis, Joshua C.;
    • Longstreth, W.T.;
    • Ikram, M. Arfan
    Publication type:
    journal article
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    Issue Information - TOC.

    Published in:
    Annals of Neurology, 2017, v. 81, n. 3, p. n/a, doi. 10.1002/ana.24918
    Publication type:
    Article
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    Reply.

    Published in:
    2017
    By:
    • Carpio, Arturo;
    • Fleury, Agnès;
    • Romo, Matthew L.;
    • Sander, Josemir W.;
    • Fleury, Agnès
    Publication type:
    Letter
    16

    Genetics and genotype-phenotype correlations in early onset epileptic encephalopathy with burst suppression.

    Published in:
    2017
    By:
    • Olson, Heather E.;
    • Kelly, McKenna;
    • LaCoursiere, Christopher M.;
    • Pinsky, Rebecca;
    • Tambunan, Dimira;
    • Shain, Catherine;
    • Ramgopal, Sriram;
    • Takeoka, Masanori;
    • Libenson, Mark H.;
    • Julich, Kristina;
    • Loddenkemper, Tobias;
    • Marsh, Eric D.;
    • Segal, Devorah;
    • Koh, Susan;
    • Salman, Michael S.;
    • Paciorkowski, Alex R.;
    • Yang, Edward;
    • Bergin, Ann M.;
    • Sheidley, Beth Rosen;
    • Poduri, Annapurna
    Publication type:
    journal article
    17

    Typical and atypical pathology in primary progressive aphasia variants.

    Published in:
    2017
    By:
    • Spinelli, Edoardo G.;
    • Mandelli, Maria Luisa;
    • Miller, Zachary A.;
    • Santos‐Santos, Miguel A;
    • Wilson, Stephen M.;
    • Agosta, Federica;
    • Grinberg, Lea T.;
    • Huang, Eric J.;
    • Trojanowski, John Q.;
    • Meyer, Marita;
    • Henry, Maya L.;
    • Comi, Giancarlo;
    • Rabinovici, Gil;
    • Rosen, Howard J.;
    • Filippi, Massimo;
    • Miller, Bruce L.;
    • Seeley, William W.;
    • Gorno‐Tempini, Maria Luisa
    Publication type:
    journal article
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    Reply.

    Published in:
    2017
    By:
    • Elmer, Jonathan;
    • Rittenberger, Jon C.;
    • Callaway, Clifton W.;
    • Baldwin, Maria
    Publication type:
    Letter
    20

    Recessive MYPN mutations cause cap myopathy with occasional nemaline rods.

    Published in:
    2017
    By:
    • Lornage, Xavière;
    • Malfatti, Edoardo;
    • Chéraud, Chrystel;
    • Schneider, Raphaël;
    • Biancalana, Valérie;
    • Cuisset, Jean‐Marie;
    • Garibaldi, Matteo;
    • Eymard, Bruno;
    • Fardeau, Michel;
    • Boland, Anne;
    • Deleuze, Jean‐François;
    • Thompson, Julie;
    • Carlier, Robert‐Yves;
    • Böhm, Johann;
    • Romero, Norma B.;
    • Laporte, Jocelyn
    Publication type:
    journal article
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