Publicaciones en colaboración con investigadoras/es de Universitat de Barcelona (4)

2018

  1. Sporadic Creutzfeldt–Jakob disease with glial PrPRes nuclear and perinuclear immunoreactivity

    Neuropathology, Vol. 38, Núm. 5, pp. 561-567

2017

  1. Fatal Familial Insomnia: Clinical Aspects and Molecular Alterations

    Current Neurology and Neuroscience Reports, Vol. 17, Núm. 4

  2. Fatal familial insomnia: mitochondrial and protein synthesis machinery decline in the mediodorsal thalamus

    Brain Pathology, Vol. 27, Núm. 1, pp. 95-106

2005

  1. A novel mutation (K317M) in the MAPT gene causes FTDP and motor neuron disease

    Neurology, Vol. 64, Núm. 9, pp. 1578-1585