Works matching IS 08853185 AND DT 2018 AND VI 33 AND IP 7


Results: 30
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    Young-onset multiple system atrophy: Clinical and pathological features.

    Published in:
    2018
    By:
    • Batla, Amit;
    • De Pablo‐Fernandez, Eduardo;
    • Erro, Roberto;
    • Reich, Martin;
    • Calandra‐Buonaura, Giovanna;
    • Barbosa, Pedro;
    • Balint, Bettina;
    • Ling, Helen;
    • Islam, Saiful;
    • Cortelli, Pietro;
    • Volkmann, Jens;
    • Quinn, Niall;
    • Holton, Janice L.;
    • Warner, Thomas T.;
    • Bhatia, Kailash P.;
    • De Pablo-Fernandez, Eduardo;
    • Calandra-Buonaura, Giovanna
    Publication type:
    journal article
    11

    Erratum.

    Published in:
    2018
    Publication type:
    journal article
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    Structural and metabolic brain correlates of apathy in Huntington's disease.

    Published in:
    2018
    By:
    • Martínez‐Horta, Saul;
    • Perez‐Perez, Jesús;
    • Sampedro, Frederic;
    • Pagonabarraga, Javier;
    • Horta‐Barba, Andrea;
    • Carceller‐Sindreu, Mar;
    • Gomez‐Anson, Beatriz;
    • Lozano‐Martinez, Gloria Andrea;
    • Lopez‐Mora, Diego Alfonso;
    • Camacho, Valle;
    • Fernández‐León, Alejandro;
    • Carrió, Ignasi;
    • Kulisevsky, Jaime;
    • Martínez-Horta, Saul;
    • Perez-Perez, Jesús;
    • Horta-Barba, Andrea;
    • Carceller-Sindreu, Mar;
    • Gomez-Anson, Beatriz;
    • Lozano-Martinez, Gloria Andrea;
    • Lopez-Mora, Diego Alfonso
    Publication type:
    journal article
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    The genetic nomenclature of recessive cerebellar ataxias.

    Published in:
    2018
    By:
    • Rossi, Malco;
    • Anheim, Mathieu;
    • Durr, Alexandra;
    • Klein, Christine;
    • Koenig, Michel;
    • Synofzik, Matthis;
    • Marras, Connie;
    • van de Warrenburg, Bart P.;
    • on behalf of the International Parkinson and Movement Disorder Society Task Force on Classification and Nomenclature of Genetic Movement Disorders;
    • International Parkinson and Movement Disorder Society Task Force on Classification and Nomenclature of Genetic Movement Disorders
    Publication type:
    journal article
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    Genotype-phenotype correlations, dystonia and disease progression in spinocerebellar ataxia type 14.

    Published in:
    2018
    By:
    • Chelban, Viorica;
    • Wiethoff, Sarah;
    • Fabian‐Jessing, Bjørn K.;
    • Haridy, Nourelhoda A.;
    • Khan, Alaa;
    • Efthymiou, Stephanie;
    • Becker, Esther B. E.;
    • O'Connor, Emer;
    • Hersheson, Joshua;
    • Newland, Katrina;
    • Hojland, Allan Thomas;
    • Gregersen, Pernille A.;
    • Lindquist, Suzanne G.;
    • Petersen, Michael B.;
    • Nielsen, Jørgen E.;
    • Nielsen, Michael;
    • Wood, Nicholas W.;
    • Giunti, Paola;
    • Houlden, Henry;
    • Fabian-Jessing, Bjørn K
    Publication type:
    journal article
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    Deep brain stimulation treated dystonia-trajectory via status dystonicus.

    Published in:
    2018
    By:
    • Nerrant, Elodie;
    • Gonzalez, Victoria;
    • Milesi, Christophe;
    • Vasques, Xavier;
    • Ruge, Diane;
    • Roujeau, Thomas;
    • De Antonio Rubio, Isabel;
    • Cyprien, Fabienne;
    • Seng, Emilie Chan;
    • Demailly, Diane;
    • Roubertie, Agathe;
    • Boularan, Alain;
    • Greco, Fréderic;
    • Perrigault, Pierre‐François;
    • Cambonie, Gilles;
    • Coubes, Philippe;
    • Cif, Laura;
    • Perrigault, Pierre-François
    Publication type:
    journal article
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    Issue Information.

    Published in:
    Movement Disorders, 2018, v. 33, n. 7, p. 1, doi. 10.1002/mds.27158
    Publication type:
    Article