P.
Pastor
Publicaciones en las que colabora con P. Pastor (22)
2023
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Brainstem neuromelanin and iron MRI reveals a precise signature for idiopathic and LRRK2 Parkinson’s disease
npj Parkinson's Disease, Vol. 9, Núm. 1
2021
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Exome-wide rare variant analysis in familial essential tremor
Parkinsonism and Related Disorders, Vol. 82, pp. 109-116
2019
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Dynamic atlas-based segmentation and quantification of neuromelanin-rich brainstem structures in Parkinson disease
IEEE Transactions on Medical Imaging, Vol. 38, Núm. 3, pp. 813-823
2016
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A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer’s disease
Acta Neuropathologica, Vol. 132, Núm. 2, pp. 213-224
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Neuroimaging Correlates of Frontotemporal Dementia Associated with SQSTM1 Mutations
Journal of Alzheimer's Disease, Vol. 53, Núm. 1, pp. 303-313
2015
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Atlas-based segmentation of brainstem regions in neuromelanin-sensitive magnetic resonance images
Progress in Biomedical Optics and Imaging - Proceedings of SPIE
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Automated Neuromelanin Imaging as a Diagnostic Biomarker for Parkinson's Disease
Movement Disorders, Vol. 30, Núm. 7, pp. 945-952
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Genetic variability in SQSTM1 and risk of early-onset Alzheimer dementia: A European early-onset dementia consortium study
Neurobiology of Aging, Vol. 36, Núm. 5, pp. 2005.e15-2005.e22
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MAPT H1 haplotype is associated with late-onset Alzheimer's disease risk in APOE ε 4 noncarriers: Results from the dementia genetics Spanish consortium
Journal of Alzheimer's Disease, Vol. 49, Núm. 2, pp. 343-352
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Rare Variants in PLD3 Do Not Affect Risk for Early-Onset Alzheimer Disease in a European Consortium Cohort
Human Mutation, Vol. 36, Núm. 12, pp. 1226-1235
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TREM2 R47H variant and risk of essential tremor: A cross-sectional international multicenter study
Parkinsonism and Related Disorders, Vol. 21, Núm. 3, pp. 306-309
2014
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Frontobasal gray matter loss is associated with the TREM2 p.R47H variant
Neurobiology of Aging, Vol. 35, Núm. 12, pp. 2681-2690
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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
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Fused in sarcoma (FUS) gene mutations are not a frequent cause of essential tremor in europeans
Neurobiology of Aging, Vol. 34, Núm. 10, pp. 2441.e9-2441.e11
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Selective brain gray matter atrophy associated with APOE ε4 and MAPT H1 in subjects with mild cognitive impairment
Journal of Alzheimer's Disease, Vol. 33, Núm. 4, pp. 1009-1019
2012
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LRRK2 haplotype-sharing analysis in Parkinson's disease reveals a novel p.S1761R mutation
Movement Disorders, Vol. 27, Núm. 1, pp. 146-150
2010
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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
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PINK1-linked parkinsonism is associated with Lewy body pathology
Brain, Vol. 133, Núm. 4, pp. 1128-1142
2009
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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
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Cortical atrophy and language network reorganization associated with a novel progranulin mutation
Cerebral Cortex, Vol. 19, Núm. 8, pp. 1751-1760