Neurociencias
Departamento
A.
Gorostidi Pagola
Publicaciones en las que colabora con A. Gorostidi Pagola (44)
2023
2022
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Endothelial NO synthase 786T/T polymorphism increases hemorrhagic transformation after endovascular thrombectomy
Nitric Oxide - Biology and Chemistry, Vol. 129, pp. 8-15
2021
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A More Homogeneous Phenotype in Parkinson's Disease Related to R1441G Mutation in the LRRK2 Gene
Frontiers in Neurology, Vol. 12
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Clinical and Genetic Analysis of Costa Rican Patients With Parkinson's Disease
Frontiers in Neurology, Vol. 12
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R1441G but not G2019S mutation enhances LRRK2 mediated Rab10 phosphorylation in human peripheral blood neutrophils
Acta Neuropathologica, Vol. 142, Núm. 3, pp. 475-494
2019
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The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population-Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight
Movement Disorders, Vol. 34, Núm. 12, pp. 1851-1863
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Using global team science to identify genetic parkinson's disease worldwide
Annals of Neurology
2018
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LRP10 in α-synucleinopathies
The Lancet Neurology
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Ratios of proteins in cerebrospinal fluid in Parkinson's disease cognitive decline: prospective study
Movement Disorders, Vol. 33, Núm. 11, pp. 1809-1813
2017
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Progressive changes in non-coding RNA profile in leucocytes with age
Aging, Vol. 9, Núm. 4, pp. 1202-1218
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Tau/α-synuclein ratio and inflammatory proteins in Parkinson's disease: An exploratory study
Movement Disorders, Vol. 32, Núm. 7, pp. 1066-1073
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The unexpected co-occurrence of GRN and MAPT p.A152T in Basque families: Clinical and pathological characteristics
PLoS ONE, Vol. 12, Núm. 6
2016
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Assessing the role of TUBA4A gene in frontotemporal degeneration
Neurobiology of Aging, Vol. 38, pp. 215.e13-215.e14
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DAT imaging and clinical biomarkers in relatives at genetic risk for LRRK2R1441G Parkinson's disease
Movement Disorders, Vol. 31, Núm. 3, pp. 335-343
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Genetic Mutation Analysis of Parkinson’s Disease Patients Using Multigene Next-Generation Sequencing Panels
Molecular Diagnosis and Therapy, Vol. 20, Núm. 5, pp. 481-491
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Mutations in LRRK2 impair NF-ΚB pathway in iPSC-derived neurons
Journal of Neuroinflammation, Vol. 13, Núm. 1
2015
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Analysis of the CHCHD10 gene in patients with frontotemporal dementia and amyotrophic lateral sclerosis from Spain
Brain
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GIGYF2 mutation in late-onset Parkinson's disease with cognitive impairment
Journal of Human Genetics, Vol. 60, Núm. 10, pp. 637-640
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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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SCN4A pore mutation pathogenetically contributes to autosomal dominant essential tremor and may increase susceptibility to epilepsy
Human Molecular Genetics, Vol. 24, Núm. 24, pp. 7111-7120