Works matching IS 00068950 AND DT 2016 AND VI 139 AND IP 1


Results: 37
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    Corrigendum.

    Published in:
    2016
    Publication type:
    corrected article
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    ALDH18A1 gene mutations cause dominant spastic paraplegia SPG9: loss of function effect and plausibility of a dominant negative mechanism.

    Published in:
    2016
    By:
    • Panza, Emanuele;
    • Escamilla-Honrubia, Juan M.;
    • Marco-Marín, Clara;
    • Gougeard, Nadine;
    • De Michele, Giuseppe;
    • Morra, Vincenzo Brescia;
    • Liguori, Rocco;
    • Salviati, Leonardo;
    • Donati, Maria Alice;
    • Cusano, Roberto;
    • Pippucci, Tommaso;
    • Ravazzolo, Roberto;
    • Németh, Andrea H.;
    • Smithson, Sarah;
    • Davies, Sally;
    • Hurst, Jane A.;
    • Bordo, Domenico;
    • Rubio, Vicente;
    • Seri, Marco;
    • Coutelier, Marie
    Publication type:
    Letter
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    Early detection of intentional harm in the human amygdala.

    Published in:
    2016
    By:
    • Hesse, Eugenia;
    • Mikulan, Ezequiel;
    • Decety, Jean;
    • Sigman, Mariano;
    • del Carmen Garcia, María;
    • Silva, Walter;
    • Ciraolo, Carlos;
    • Vaucheret, Esteban;
    • Baglivo, Fabricio;
    • Huepe, David;
    • Lopez, Vladimir;
    • Manes, Facundo;
    • Bekinschtein, Tristan A.;
    • Ibanez, Agustin;
    • Garcia, María Del Carmen
    Publication type:
    journal article
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    Mutations in the MORC2 gene cause axonal Charcot-Marie-Tooth disease.

    Published in:
    2016
    By:
    • Sevilla, Teresa;
    • Lupo, Vincenzo;
    • Martínez-Rubio, Dolores;
    • Sancho, Paula;
    • Sivera, Rafael;
    • Chumillas, María J.;
    • García-Romero, Mar;
    • Pascual-Pascual, Samuel I.;
    • Muelas, Nuria;
    • Dopazo, Joaquín;
    • Vílchez, Juan J.;
    • Palau, Francesc;
    • Espinós, Carmen
    Publication type:
    journal article
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    EDITORIAL.

    Published in:
    Brain: A Journal of Neurology, 2016, v. 139, n. 1, p. 1, doi. 10.1093/brain/awv377
    By:
    • Kullmann, Dimitri M.
    Publication type:
    Article