Publicaciones en las que colabora con P. Pastor (9)

2015

  1. Descripción de una serie de pacientes con diagnóstico de enfermedad priónica

    Neurologia, Vol. 30, Núm. 3, pp. 144-152

2014

  1. Investigation of the role of rare TREM2 variants in frontotemporal dementia subtypes

    Neurobiology of Aging, Vol. 35, Núm. 11, pp. 2657.e13-2657.e19

2013

  1. Automated analysis of FDG PET as a tool for single-subject probabilistic prediction and detection of Alzheimer's disease dementia

    European Journal of Nuclear Medicine and Molecular Imaging, Vol. 40, Núm. 9, pp. 1394-1405

2012

  1. Usefulness of positron emission tomography with fludeoxyglucose F 18 and with carbon 11-tagged methionine in the diagnosis of hippocampal lesions

    Archives of Neurology, Vol. 69, Núm. 12, pp. 1652-1653

2010

  1. Analysis of the GIGYF2 gene in familial and sporadic Parkinson disease in the Spanish population

    European Journal of Neurology, Vol. 17, Núm. 2, pp. 321-325

2009

  1. 5′-upstream variants of CRHR1 and MAPT genes associated with age at onset in progressive supranuclear palsy and cortical basal degeneration

    Neurobiology of Disease, Vol. 33, Núm. 2, pp. 164-170

  2. Cortical atrophy and language network reorganization associated with a novel progranulin mutation

    Cerebral Cortex, Vol. 19, Núm. 8, pp. 1751-1760

  3. Forceps minor region signal abnormality "ears of the lynx": An early MRI finding in spastic paraparesis with thin corpus callosum and mutations in the spatacsin gene (SPG11) on chromosome 15

    Journal of Neuroimaging, Vol. 19, Núm. 1, pp. 52-60

2008

  1. SPG11 compound mutations in spastic paraparesis with thin corpus callosum

    Neurology, Vol. 71, Núm. 5, pp. 332-336