Publications dans lesquelles il/elle collabore avec P. Pastor (22)

2023

  1. 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

  1. Exome-wide rare variant analysis in familial essential tremor

    Parkinsonism and Related Disorders, Vol. 82, pp. 109-116

2019

  1. 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

  1. 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

  2. Neuroimaging Correlates of Frontotemporal Dementia Associated with SQSTM1 Mutations

    Journal of Alzheimer's Disease, Vol. 53, Núm. 1, pp. 303-313

2015

  1. Atlas-based segmentation of brainstem regions in neuromelanin-sensitive magnetic resonance images

    Progress in Biomedical Optics and Imaging - Proceedings of SPIE

  2. Automated Neuromelanin Imaging as a Diagnostic Biomarker for Parkinson's Disease

    Movement Disorders, Vol. 30, Núm. 7, pp. 945-952

  3. 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

  4. 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

  5. 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

  6. 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

  1. Frontobasal gray matter loss is associated with the TREM2 p.R47H variant

    Neurobiology of Aging, Vol. 35, Núm. 12, pp. 2681-2690

  2. 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. 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

  2. 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

  1. LRRK2 haplotype-sharing analysis in Parkinson's disease reveals a novel p.S1761R mutation

    Movement Disorders, Vol. 27, Núm. 1, pp. 146-150

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

  2. PINK1-linked parkinsonism is associated with Lewy body pathology

    Brain, Vol. 133, Núm. 4, pp. 1128-1142

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