ELENA LEZCANO GARCIA-rekin lankidetzan egindako argitalpenak (5)

2006

  1. Tau-predominant-associated pathology in a sporadic-late-onset Hallervorden-Spatz syndrome

    Movement Disorders, Vol. 21, Núm. 1, pp. 107-111

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. Cerebrovascular disease in a tertiary care hospital. Current situation and issues to be improved

    Revista de Neurologia, Vol. 40, Núm. 12, pp. 723-728

  3. Familial prion diseases in the basque country (Spain)

    Neuroepidemiology, Vol. 24, Núm. 1-2, pp. 103-109

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

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