Publicacións en colaboración con investigadores/as de Hospital do Meixoeiro (3)

2011

  1. A novel MYH7 mutation links congenital fiber type disproportion and myosin storage myopathy

    Neuromuscular Disorders, Vol. 21, Núm. 4, pp. 254-262

  2. Neurophysiological study in cerebrotendinous xanthomatosis

    Muscle and Nerve, Vol. 43, Núm. 4, pp. 531-536

2005

  1. Autosomal dominant congenital fibre type disproportion: A clinicopathological and imaging study of a large family

    Brain, Vol. 128, Núm. 7, pp. 1716-1727