María A. Pastor-rekin lankidetzan egindako argitalpenak (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