2005

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

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

2. Phenotypic variability in familial prion diseases due to the D178N mutation

   Journal of Neurology, Neurosurgery and Psychiatry, Vol. 76, Núm. 11, pp. 1491-1496