Resultados de búsqueda - Annick Labarre‐Vila

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  1. 1
    A homozygous splicing mutation causing a depletion of skeletal muscle RYR1 is associated with multi-minicore disease congenital myopathy with ophthalmoplegia

    A homozygous splicing mutation causing a depletion of skeletal muscle RYR1 is associated with multi-minicore disease congenital myopathy with ophthalmoplegia por Nicole Monnier, Ana Ferreiro, Isabelle Marty, Annick Labarre‐Vila, Paulette Mezin, Joël Lunardi

    Publicado 2003
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  2. 2
    Generalised sensory system abnormalities in amyotrophic lateral sclerosis: a European multicentre study

    Generalised sensory system abnormalities in amyotrophic lateral sclerosis: a European multicentre study por Kirsten Pugdahl, Anders Fuglsang‐Frederiksen, Mamede de Carvalho, Birger Johnsen, P R W Fawcett, Annick Labarre‐Vila, Rocco Liguori, W. Nix, IS Schofield

    Publicado 2006
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