Publicacións nas que colabora con María A. Pastor (8)

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

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

2003

  1. Human Cerebral Activation during Steady-State Visual-Evoked Responses

    Journal of Neuroscience, Vol. 23, Núm. 37, pp. 11621-11627

2002

  1. Activation of human cerebral and cerebellar cortex by auditory stimulation at 40 Hz

    Journal of Neuroscience, Vol. 22, Núm. 23, pp. 10501-10506