Publicaciones en las que colabora con Ainara Estanga Alustiza (7)

2016

  1. DAT imaging and clinical biomarkers in relatives at genetic risk for LRRK2R1441G Parkinson's disease

    Movement Disorders, Vol. 31, Núm. 3, pp. 335-343

2014

  1. Cognitive dysfunction in Parkinson's disease related to the R1441G mutation in LRRK2

    Parkinsonism and Related Disorders, Vol. 20, Núm. 10, pp. 1097-1100

  2. Prevalence of cancer in Parkinson's disease related to R1441G and G2019S mutations in LRRK2

    Movement Disorders, Vol. 29, Núm. 6, pp. 750-755

2013

  1. Distinctive age-related temporal cortical thinning in asymptomatic granulin gene mutation carriers

    Neurobiology of Aging, Vol. 34, Núm. 5, pp. 1462-1468

2012

  1. Neuropsychological features of asymptomatic c.709-1G>A progranulin mutation carriers

    Journal of the International Neuropsychological Society, Vol. 18, Núm. 6, pp. 1086-1090

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

2009

  1. Frontotemporoparietal dementia: Clinical phenotype associated with the c.709-1G>A PGRN mutation

    Neurology, Vol. 73, Núm. 17, pp. 1367-1374