Search Results - "CARRIERE, Nathalie"

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  1. 1
    Complicated forms of autosomal dominant hereditary spastic paraplegia are frequent in SPG10

    Complicated forms of autosomal dominant hereditary spastic paraplegia are frequent in SPG10 by Goizet, Cyril, Boukhris, Amir, Mundwiller, Emeline, Tallaksen, Chantal, Forlani, Sylvie, Toutain, Annick, Carriere, Nathalie, Paquis, Véronique, Depienne, Christel, Durr, Alexandra, Stevanin, Giovanni, Brice, Alexis

    Published in Human mutation (01-02-2009)
    “…Hereditary spastic paraplegias (HSP) constitute a heterogeneous group of neurodegenerative disorders characterized by slowly progressive spasticity of the…”
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  2. 2
    Adult-onset autosomal dominant centronuclear myopathy due to BIN1 mutations

    Adult-onset autosomal dominant centronuclear myopathy due to BIN1 mutations by BÖHM, Johann, BIANCALANA, Valérie, LAFORET, Pascal, MAISONOBE, Thierry, OLIVE, Montse, GONZALEZ-MERA, Laura, FARDEAU, Michel, CARRIERE, Nathalie, CLAVELOU, Pierre, EYMARD, Bruno, BITOUN, Marc, RENDU, John, MALFATTI, Edoardo, FAURE, Julien, WEIS, Joachim, MANDEL, Jean-Louis, ROMERO, Norma B, LAPORTE, Jocelyn, DONDAINE, Nicolas, KOCH, Catherine, VASLI, Nasim, KRESS, Wolfram, STRITTMATTER, Matthias, TARATUTO, Ana Lia, GONORAZKY, Hernan

    Published in Brain (London, England : 1878) (01-12-2014)
    “…Centronuclear myopathies are congenital muscle disorders characterized by type I myofibre predominance and an increased number of muscle fibres with nuclear…”
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