Works matching IS 00068950 AND DT 2014 AND VI 137 AND IP 12


Results: 38
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    The nature of tremor circuits in parkinsonian and essential tremor.

    Published in:
    Brain: A Journal of Neurology, 2014, v. 137, n. 12, p. 3223, doi. 10.1093/brain/awu250
    By:
    • Cagnan, Hayriye;
    • Little, Simon;
    • Foltynie, Thomas;
    • Limousin, Patricia;
    • Zrinzo, Ludvic;
    • Hariz, Marwan;
    • Cheeran, Binith;
    • Fitzgerald, James;
    • Green, Alexander L.;
    • Aziz, Tipu;
    • Brown, Peter
    Publication type:
    Article
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    Corrigendum.

    Published in:
    Brain: A Journal of Neurology, 2014, v. 137, n. 12, p. e316, doi. 10.1093/brain/awu269
    Publication type:
    Article
    9

    Novel mutations in human and mouse SCN4A implicate AMPK in myotonia and periodic paralysis.

    Published in:
    Brain: A Journal of Neurology, 2014, v. 137, n. 12, p. 3171, doi. 10.1093/brain/awu292
    By:
    • Corrochano, Silvia;
    • Männikkö, Roope;
    • Joyce, Peter I.;
    • McGoldrick, Philip;
    • Wettstein, Jessica;
    • Lassi, Glenda;
    • Raja Rayan, Dipa L.;
    • Blanco, Gonzalo;
    • Quinn, Colin;
    • Liavas, Andrianos;
    • Lionikas, Arimantas;
    • Amior, Neta;
    • Dick, James;
    • Healy, Estelle G.;
    • Stewart, Michelle;
    • Carter, Sarah;
    • Hutchinson, Marie;
    • Bentley, Liz;
    • Fratta, Pietro;
    • Cortese, Andrea
    Publication type:
    Article
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    Editorial.

    Published in:
    Brain: A Journal of Neurology, 2014, v. 137, n. 12, p. 3099, doi. 10.1093/brain/awu319
    By:
    • Kullmann, Dimitri M.
    Publication type:
    Article
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    Corrigendum.

    Published in:
    Brain: A Journal of Neurology, 2014, v. 137, n. 12, p. 1, doi. 10.1093/brain/awu274
    Publication type:
    Article
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    Connectopathy in ageing and dementia.

    Published in:
    Brain: A Journal of Neurology, 2014, v. 137, n. 12, p. 3104, doi. 10.1093/brain/awu276
    By:
    • Toga, Arthur W.;
    • Thompson, Paul M.
    Publication type:
    Article
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    Reply: Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis.

    Published in:
    Brain: A Journal of Neurology, 2014, v. 137, n. 12, p. e312, doi. 10.1093/brain/awu267
    By:
    • Bannwarth, Sylvie;
    • Ait-El-Mkadem, Samira;
    • Chaussenot, Annabelle;
    • Genin, Emmanuelle C.;
    • Lacas-Gervais, Sandra;
    • Fragaki, Konstantina;
    • Berg-Alonso, Laetitia;
    • Kageyama, Yusuke;
    • Serre, Valérie;
    • Moore, David;
    • Verschueren, Annie;
    • Rouzier, Cécile;
    • Le Ber, Isabelle;
    • Augé, Gaëlle;
    • Cochaud, Charlotte;
    • Lespinasse, Françoise;
    • N’Guyen, Karine;
    • de Septenville, Anne;
    • Brice, Alexis;
    • Yu-Wai-Man, Patrick
    Publication type:
    Article
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    Adult-onset autosomal dominant centronuclear myopathy due to BIN1 mutations.

    Published in:
    Brain: A Journal of Neurology, 2014, v. 137, n. 12, p. 3160, doi. 10.1093/brain/awu272
    By:
    • Böhm, Johann;
    • Biancalana, Valérie;
    • Malfatti, Edoardo;
    • Dondaine, Nicolas;
    • Koch, Catherine;
    • Vasli, Nasim;
    • Kress, Wolfram;
    • Strittmatter, Matthias;
    • Taratuto, Ana Lia;
    • Gonorazky, Hernan;
    • Laforêt, Pascal;
    • Maisonobe, Thierry;
    • Olivé, Montse;
    • Gonzalez-Mera, Laura;
    • Fardeau, Michel;
    • Carrière, Nathalie;
    • Clavelou, Pierre;
    • Eymard, Bruno;
    • Bitoun, Marc;
    • Rendu, John
    Publication type:
    Article
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    Reply: Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease.

    Published in:
    Brain: A Journal of Neurology, 2014, v. 137, n. 12, p. e310, doi. 10.1093/brain/awu228
    By:
    • Bannwarth, Sylvie;
    • Ait-El-Mkadem, Samira;
    • Chaussenot, Annabelle;
    • Genin, Emmanuelle C.;
    • Lacas-Gervais, Sandra;
    • Fragaki, Konstantina;
    • Berg-Alonso, Laetitia;
    • Kageyama, Yusuke;
    • Serre, Valérie;
    • Moore, David;
    • Verschueren, Annie;
    • Rouzier, Cécile;
    • Le Ber, Isabelle;
    • Augé, Gaëlle;
    • Cochaud, Charlotte;
    • Lespinasse, Françoise;
    • N’Guyen, Karine;
    • de Septenville, Anne;
    • Brice, Alexis;
    • Yu-Wai-Man, Patrick
    Publication type:
    Article
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    Unconscious relational encoding depends on hippocampus.

    Published in:
    Brain: A Journal of Neurology, 2014, v. 137, n. 12, p. 3355, doi. 10.1093/brain/awu270
    By:
    • Duss, Simone B.;
    • Reber, Thomas P.;
    • Hänggi, Jürgen;
    • Schwab, Simon;
    • Wiest, Roland;
    • Müri, René M.;
    • Brugger, Peter;
    • Gutbrod, Klemens;
    • Henke, Katharina
    Publication type:
    Article
    36

    White matter involvement in sporadic Creutzfeldt-Jakob disease.

    Published in:
    Brain: A Journal of Neurology, 2014, v. 137, n. 12, p. 3339, doi. 10.1093/brain/awu298
    By:
    • Caverzasi, Eduardo;
    • Mandelli, Maria Luisa;
    • DeArmond, Stephen J.;
    • Hess, Christopher P.;
    • Vitali, Paolo;
    • Papinutto, Nico;
    • Oehler, Abby;
    • Miller, Bruce L.;
    • Lobach, Irina V.;
    • Bastianello, Stefano;
    • Geschwind, Michael D.;
    • Henry, Roland G.
    Publication type:
    Article
    37

    Reply: Are CHCHD10 mutations indeed associated with familial amyotrophic lateral sclerosis?

    Published in:
    Brain: A Journal of Neurology, 2014, v. 137, n. 12, p. e314, doi. 10.1093/brain/awu300
    By:
    • Bannwarth, Sylvie;
    • Ait-El-Mkadem, Samira;
    • Chaussenot, Annabelle;
    • Genin, Emmanuelle C.;
    • Lacas-Gervais, Sandra;
    • Fragaki, Konstantina;
    • Berg-Alonso, Laetitia;
    • Kageyama, Yusuke;
    • Serre, Valérie;
    • Moore, David;
    • Verschueren, Annie;
    • Rouzier, Cécile;
    • Le Ber, Isabelle;
    • Augé, Gaëlle;
    • Cochaud, Charlotte;
    • Lespinasse, Françoise;
    • N’Guyen, Karine;
    • de Septenville, Anne;
    • Brice, Alexis;
    • Yu-Wai-Man, Patrick
    Publication type:
    Article
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