Publicaciones en colaboración con investigadoras/es de Instituto Vasco de Investigación y Desarrollo Agrario (12)

2018

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

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

2015

  1. Coexistence of mixed phenotype Creutzfeldt-Jakob disease, Lewy body disease and argyrophilic grain disease plus histological features of possible Alzheimer's disease: A multi-protein disorder in an autopsy case

    Neuropathology, Vol. 35, Núm. 1, pp. 56-63

2014

  1. Geographical analysis of the sporadic Creutzfeldt-Jakob disease distribution in the autonomous community of the Basque country for the period 1995-2008

    European Neurology, Vol. 72, Núm. 1-2, pp. 20-25

2013

  1. A novel form of human disease

    Prion Biology: Research and Advances (Apple Academic Press), pp. 179-210

  2. Evaluation of the efficacy of oxytetracycline treatment followed by vaccination against Q fever in a highly infected sheep flock

    Veterinary Journal, Vol. 196, Núm. 1, pp. 81-85

2012

  1. Coexistence of protease sensitive and resistant prion protein in 129VV homozygous sporadic Creutzfeldt-Jakob disease: A case report

    Journal of Medical Case Reports, Vol. 6

  2. Estimation of Coxiella burnetii prevalence in dairy cattle in intensive systems by serological and molecular analyses of bulk-tank milk samples

    Journal of Dairy Science, Vol. 95, Núm. 4, pp. 1632-1638

  3. Genotyping of Coxiella burnetii from domestic ruminants in northern Spain

    BMC Veterinary Research, Vol. 8

  4. Molecular method for the characterization of Coxiella burnetii from clinical and environmental samples: Variability of genotypes in Spain

    BMC Microbiology, Vol. 12

2010

  1. A Novel PRNP Y218N mutation in gerstmann-sträussler-scheinker disease with neurofibrillary degeneration

    Journal of Neuropathology and Experimental Neurology, Vol. 69, Núm. 8, pp. 789-800

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

    BMC neurology, Vol. 10, pp. 99

  3. Somatic mosaicism in a case of apparently sporadic Creutzfeldt-Jakob disease carrying a de novo D178N mutation in the PRNP gene

    American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, Vol. 153, Núm. 7, pp. 1283-1291