Publicaciones en colaboración con investigadores/as de Instituto de Investigaciones Biomédicas Alberto Sols (6)

2008

  1. OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes

    Brain, Vol. 131, Núm. 2, pp. 338-351

2007

  1. Mild ocular myopathy associated with a novel mutation in mitochondrial twinkle helicase

    Neuromuscular Disorders, Vol. 17, Núm. 9-10, pp. 677-680

2001

  1. Early-onset multisystem mitochondrial disorder caused by a nonsense mutation in the mitochondrial DNA cytochrome C oxidase II gene

    Annals of Neurology, Vol. 50, Núm. 3, pp. 409-413

  2. Thyroid hormone regulates oxidative phosphorylation in the cerebral cortex and striatum of neonatal rats

    Journal of Neurochemistry, Vol. 78, Núm. 5, pp. 1054-1063

2000

  1. The pathogenic role of point mutations affecting the translational initiation codon of mitochondrial genes

    Molecular Genetics and Metabolism, Vol. 70, Núm. 3, pp. 238-240

1998

  1. Mitochondrial gene expression and respiratory enzyme activities in cardiac diseases

    Biochimica et Biophysica Acta - Molecular Basis of Disease, Vol. 1406, Núm. 1, pp. 85-90