Ana Belén Rodríguez-Martínez

A novel mutation (K317M) in the <i>MAPT</i> gene causes FTDP and motor neuron disease

J.J. Zarranz, Isidró Ferrer, E. Lezcano et al. · Neurology · 2005 · 100 citations

A Novel<i>PRNP Y218N</i>Mutation in Gerstmann-Sträussler-Scheinker Disease With Neurofibrillary Degeneration

Ainhoa Alzualde, Begoña Indakoetxea, Isidró Ferrer et al. · Journal of Neuropathology & Experimental Neurology · 2010 · 54 citations · Full text

Creutzfeldt-jakob Disease, Genetics, Proteasome +20

Validation of the Minnesota Living With Heart Failure Questionnaire in Primary Care

José Cesáreo Naveiro Rilo, D. Diez-Juárez, Agustín Romero Blanco et al. · Revista Española de Cardiología (English Edition) · 2010 · 45 citations

Family Medicine, Family Health, Heart Failure +12

Somatic mosaicism in a case of apparently sporadic Creutzfeldt‐Jakob disease carrying a de novo D178N mutation in the <i>PRNP</i> gene

Ainhoa Alzualde, Fermín Moreno, Pablo Martínez‐Lage et al. · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 2010 · 38 citations · Full text

A novel form of human disease with a protease-sensitive prion protein and heterozygosity methionine/valine at codon 129: Case report

Ana Belén Rodríguez-Martínez, Joseba M. Garrido, J.J. Zarranz et al. · BMC Neurology · 2010 · 36 citations · Full text