Works matching IS 00068950 AND DT 2013 AND VI 136 AND IP 11

Results: 38
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    Large scale genotype-phenotype analyses indicate that novel prognostic tools are required for families with facioscapulohumeral muscular dystrophy.

    Published in:
    2013
    By:
    • Ricci, Giulia;
    • Scionti, Isabella;
    • Sera, Francesco;
    • Govi, Monica;
    • D'Amico, Roberto;
    • Frambolli, Ilaria;
    • Mele, Fabiano;
    • Filosto, Massimiliano;
    • Vercelli, Liliana;
    • Ruggiero, Lucia;
    • Berardinelli, Angela;
    • Angelini, Corrado;
    • Antonini, Giovanni;
    • Bucci, Elisabetta;
    • Cao, Michelangelo;
    • Daolio, Jessica;
    • Di Muzio, Antonio;
    • Di Leo, Rita;
    • Galluzzi, Giuliana;
    • Iannaccone, Elisabetta
    Publication type:
    journal article
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    Cutaneous allodynia as a predictor of migraine chronification.

    Published in:
    Brain: A Journal of Neurology, 2013, v. 136, n. 11, p. 3489, doi. 10.1093/brain/awt251
    By:
    • Louter, Mark A.;
    • Bosker, Johanneke E.;
    • van Oosterhout, Willebrordus P. J.;
    • van Zwet, Erik W.;
    • Zitman, Frans G.;
    • Ferrari, Michel D.;
    • Terwindt, Gisela M.
    Publication type:
    Article
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    Some painful perspectives on pain.

    Published in:
    Brain: A Journal of Neurology, 2013, v. 136, n. 11, p. 3511, doi. 10.1093/brain/awt240
    By:
    • Schott, G. D.
    Publication type:
    Article
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    Large scale genotype–phenotype analyses indicate that novel prognostic tools are required for families with facioscapulohumeral muscular dystrophy.

    Published in:
    Brain: A Journal of Neurology, 2013, v. 136, n. 11, p. 3408, doi. 10.1093/brain/awt226
    By:
    • Ricci, Giulia;
    • Scionti, Isabella;
    • Sera, Francesco;
    • Govi, Monica;
    • D’Amico, Roberto;
    • Frambolli, Ilaria;
    • Mele, Fabiano;
    • Filosto, Massimiliano;
    • Vercelli, Liliana;
    • Ruggiero, Lucia;
    • Berardinelli, Angela;
    • Angelini, Corrado;
    • Antonini, Giovanni;
    • Bucci, Elisabetta;
    • Cao, Michelangelo;
    • Daolio, Jessica;
    • Di Muzio, Antonio;
    • Di Leo, Rita;
    • Galluzzi, Giuliana;
    • Iannaccone, Elisabetta
    Publication type:
    Article
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    Phenotypic spectrum of probable and genetically-confirmed idiopathic basal ganglia calcification.

    Published in:
    Brain: A Journal of Neurology, 2013, v. 136, n. 11, p. 3395, doi. 10.1093/brain/awt255
    By:
    • Nicolas, Gaël;
    • Pottier, Cyril;
    • Charbonnier, Camille;
    • Guyant-Maréchal, Lucie;
    • Le Ber, Isabelle;
    • Pariente, Jérémie;
    • Labauge, Pierre;
    • Ayrignac, Xavier;
    • Defebvre, Luc;
    • Maltête, David;
    • Martinaud, Olivier;
    • Lefaucheur, Romain;
    • Guillin, Olivier;
    • Wallon, David;
    • Chaumette, Boris;
    • Rondepierre, Philippe;
    • Derache, Nathalie;
    • Fromager, Guillaume;
    • Schaeffer, Stéphane;
    • Krystkowiak, Pierre
    Publication type:
    Article
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    From The Archives.

    Published in:
    Brain: A Journal of Neurology, 2013, v. 136, n. 11, p. 3209, doi. 10.1093/brain/awt298
    By:
    • Compston, Alastair
    Publication type:
    Article
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    Circular inferences in schizophrenia.

    Published in:
    Brain: A Journal of Neurology, 2013, v. 136, n. 11, p. 3227, doi. 10.1093/brain/awt257
    By:
    • Jardri, Renaud;
    • Denève, Sophie
    Publication type:
    Article
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    RAD51 deficiency disrupts the corticospinal lateralization of motor control.

    Published in:
    Brain: A Journal of Neurology, 2013, v. 136, n. 11, p. 3333, doi. 10.1093/brain/awt258
    By:
    • Gallea, Cécile;
    • Popa, Traian;
    • Hubsch, Cécile;
    • Valabregue, Romain;
    • Brochard, Vanessa;
    • Kundu, Prantik;
    • Schmitt, Benoît;
    • Bardinet, Eric;
    • Bertasi, Eric;
    • Flamand-Roze, Constance;
    • Alexandre, Nicolas;
    • Delmaire, Christine;
    • Méneret, Aurélie;
    • Depienne, Christel;
    • Poupon, Cyril;
    • Hertz-Pannier, Lucie;
    • Cincotta, Massimo;
    • Vidailhet, Marie;
    • Lehericy, Stéphane;
    • Meunier, Sabine
    Publication type:
    Article
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    Periventricular heterotopia in 6q terminal deletion syndrome: role of the C6orf70 gene.

    Published in:
    Brain: A Journal of Neurology, 2013, v. 136, n. 11, p. 3378, doi. 10.1093/brain/awt249
    By:
    • Conti, Valerio;
    • Carabalona, Aurelie;
    • Pallesi-Pocachard, Emilie;
    • Parrini, Elena;
    • Leventer, Richard J.;
    • Buhler, Emmanuelle;
    • McGillivray, George;
    • Michel, François J.;
    • Striano, Pasquale;
    • Mei, Davide;
    • Watrin, Françoise;
    • Lise, Stefano;
    • Pagnamenta, Alistair T.;
    • Taylor, Jenny C.;
    • Kini, Usha;
    • Clayton-Smith, Jill;
    • Novara, Francesca;
    • Zuffardi, Orsetta;
    • Dobyns, William B.;
    • Scheffer, Ingrid E.
    Publication type:
    Article
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    Editorial.

    Published in:
    Brain: A Journal of Neurology, 2013, v. 136, n. 11, p. 3205, doi. 10.1093/brain/awt307
    By:
    • Compston, Alastair
    Publication type:
    Article
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    A positron emission tomography study of nigro-striatal dopaminergic mechanisms underlying attention: implications for ADHD and its treatment.

    Published in:
    Brain: A Journal of Neurology, 2013, v. 136, n. 11, p. 3252, doi. 10.1093/brain/awt263
    By:
    • del Campo, Natalia;
    • Fryer, Tim D.;
    • Hong, Young T.;
    • Smith, Rob;
    • Brichard, Laurent;
    • Acosta-Cabronero, Julio;
    • Chamberlain, Samuel R.;
    • Tait, Roger;
    • Izquierdo, David;
    • Regenthal, Ralf;
    • Dowson, Jonathan;
    • Suckling, John;
    • Baron, Jean-Claude;
    • Aigbirhio, Franklin I.;
    • Robbins, Trevor W.;
    • Sahakian, Barbara J.;
    • Müller, Ulrich
    Publication type:
    Article
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