3 results for author:"Atares B." in Literature citations
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| A novel PRNP Y218N mutation in Gerstmann-Straussler-Scheinker disease with neurofibrillary degeneration. Alzualde A., Indakoetxea B., Ferrer I., Moreno F., Barandiaran M., Gorostidi A., Estanga A., Ruiz I., Calero M., van Leeuwen F.W. et al. J. Neuropathol. Exp. Neurol. 69:789-800(2010) · Mapped (19) |
| A novel mutation (K317M) in the MAPT gene causes FTDP and motor neuron disease. Zarranz J.J., Ferrer I., Lezcano E., Forcadas M.I., Eizaguirre B., Atares B., Puig B., Gomez-Esteban J.C., Fernandez-Maiztegui C., Rouco I. et al. Neurology 64:1578-1585(2005) · UniProtKB (1) |
| The new mutation, E46K, of alpha-synuclein causes Parkinson and Lewy body dementia. Zarranz J.J., Alegre J., Gomez-Esteban J.C., Lezcano E., Ros R., Ampuero I., Vidal L., Hoenicka J., Rodriguez O., Atares B. et al. Ann. Neurol. 55:164-173(2004) · UniProtKB (1) |