Publicaciones en colaboración con investigadores/as de Hospital do Meixoeiro (4)

2006

  1. Association of novel POLG mutations and multiple mitochondrial DNA deletions with variable clinical phenotypes in a Spanish population

    Archives of Neurology, Vol. 63, Núm. 1, pp. 107-111

2003

  1. Unusual clinical findings and Complex III deficiency in a family with myotonic dystrophy

    Journal of the Neurological Sciences, Vol. 208, Núm. 1-2, pp. 87-91

2001

  1. Molecular heterogeneity of myophosphorylase deficiency (McArdle's disease): A genotype-phenotype correlation study

    Annals of Neurology, Vol. 50, Núm. 5, pp. 574-581

1996

  1. Single large-scale mitochondrial DNA deletion in a patient with mitochondrial myopathy associated with multiple symmetric lipomatosis

    Neurology, Vol. 47, Núm. 4, pp. 1012-1014