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Parkinsonism and spastic paraplegia type 7: Expanding the spectrum of mitochondrial Parkinsonism

Movement disorders, 2019-10, Vol.34 (10), p.1547-1561

2019

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HTT gene intermediate alleles in neurodegeneration: evidence for association with Alzheimer's disease

Neurobiology of aging, 2019-04, Vol.76, p.215.e9-215.e14

2019

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MiRNA Profile in the Substantia Nigra of Parkinson’s Disease and Healthy Subjects

Journal of molecular neuroscience, 2014-12, Vol.54 (4), p.830-836

2014

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Huntingtin CAG repeats in neuropathologically confirmed tauopathies: Novel insights

Brain pathology (Zurich, Switzerland), 2024-07, Vol.34 (4), p.e13250-n/a

2024

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Analysis of the CHCHD10 gene in patients with frontotemporal dementia and amyotrophic lateral sclerosis from Spain

Brain (London, England : 1878), 2015-12, Vol.138 (Pt 12), p.e400-e400

2015

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Genetic variation in APOE, GRN, and TP53 are phenotype modifiers in frontotemporal dementia

Neurobiology of aging, 2021-03, Vol.99, p.99.e15-99.e22

2021

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Mutational screening of the mortalin gene (HSPA9) in Parkinson’s disease

Journal of Neural Transmission, 2009-10, Vol.116 (10), p.1289-1293

2009

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Mitochondrial DNA polymorphisms and risk of Parkinson's disease in Spanish population

Journal of the neurological sciences, 2005-09, Vol.236 (1), p.49-54

2005

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Replication by the Epistasis Project of the interaction between the genes for IL-6 and IL-10 in the risk of Alzheimer's disease

Journal of neuroinflammation, 2009-08, Vol.6 (1), p.22-22

2009

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Late-onset Alzheimer's disease is associated with mitochondrial DNA 7028C/haplogroup H and D310 poly-C tract heteroplasmy

Neurogenetics, 2011-11, Vol.12 (4), p.345-346

2011

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Chemokines (RANTES and MCP-1) and chemokine-receptors (CCR2 and CCR5) gene polymorphisms in Alzheimer's and Parkinson's disease

Neuroscience letters, 2004-11, Vol.370 (2), p.151-154

2004

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Association between the A-1438G polymorphism of the serotonin 2A receptor gene and nonimpulsive suicide attempts

Psychiatric genetics, 2008-10, Vol.18 (5), p.213-218

2008

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Understanding drug-induced parkinsonism: separating pearls from oy-sters

Neurology, 2008-02, Vol.70 (8), p.e32

2008

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Amyloid Precursor Protein Gene (APP) Variation in Late-Onset Alzheimer’s Disease

Journal of molecular neuroscience, 2011-09, Vol.45 (1), p.5-9

2011

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Hyposmia in Parkinson's disease

Psychiatry and clinical neurosciences, 2012-06, Vol.66 (4), p.370-370

2012

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Myocyte enhancing factor-2A in Alzheimer's disease: Genetic analysis and association with MEF2A-polymorphisms

Neuroscience letters, 2007-01, Vol.411 (1), p.47-51

2007

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Assessing the role of TUBA4A gene in frontotemporal degeneration

Neurobiology of aging, 2016-02, Vol.38, p.215.e13-215.e14

2016

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Lack of association between protocadherin 11-X/Y ( PCDH11X and PCDH11Y ) polymorphisms and late onset Alzheimer's disease

Brain research, 2011-04, Vol.1383, p.252-256

2011

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Mutational spectrum of the SPG4 (SPAST) and SPG3A (ATL1) genes in Spanish patients with hereditary spastic paraplegia

BMC neurology, 2010-10, Vol.10 (1), p.89-89, Article 89

2010

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No differential DNA methylation of PARK2 in brain of Parkinson's disease patients and healthy controls

Movement disorders, 2013-12, Vol.28 (14), p.2032-2033

2013

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Alpha-synuclein transcript isoforms in three different brain regions from Parkinson's disease and healthy subjects in relation to the SNCA rs356165/rs11931074 polymorphisms

Neuroscience letters, 2014-03, Vol.562, p.45-49

2014

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Parkinsonism and spastic paraplegia type 7: Expanding the spectrum of mitochondrial Parkinsonism

HTT gene intermediate alleles in neurodegeneration: evidence for association with Alzheimer's disease

MiRNA Profile in the Substantia Nigra of Parkinson’s Disease and Healthy Subjects

Role for ATXN1, ATXN2, and HTT intermediate repeats in frontotemporal dementia and Alzheimer's disease

Huntingtin CAG repeats in neuropathologically confirmed tauopathies: Novel insights

Intermediate and Expanded HTT Alleles and the Risk for α‐Synucleinopathies

Assessing the role of the TREM2 p.R47H variant as a risk factor for Alzheimer's disease and frontotemporal dementia

Analysis of the CHCHD10 gene in patients with frontotemporal dementia and amyotrophic lateral sclerosis from Spain

Genetic variation in APOE, GRN, and TP53 are phenotype modifiers in frontotemporal dementia

Reply to: “Mitochondrial Parkinsonism due to SPG7/Paraplegin variants with secondary mtDNA depletion”

Mutational screening of the mortalin gene (HSPA9) in Parkinson’s disease

Mitochondrial DNA polymorphisms and risk of Parkinson's disease in Spanish population

Replication by the Epistasis Project of the interaction between the genes for IL-6 and IL-10 in the risk of Alzheimer's disease

Late-onset Alzheimer's disease is associated with mitochondrial DNA 7028C/haplogroup H and D310 poly-C tract heteroplasmy

Chemokines (RANTES and MCP-1) and chemokine-receptors (CCR2 and CCR5) gene polymorphisms in Alzheimer's and Parkinson's disease

Association between the A-1438G polymorphism of the serotonin 2A receptor gene and nonimpulsive suicide attempts

Understanding drug-induced parkinsonism: separating pearls from oy-sters

Amyloid Precursor Protein Gene (APP) Variation in Late-Onset Alzheimer’s Disease

Hyposmia in Parkinson's disease

Myocyte enhancing factor-2A in Alzheimer's disease: Genetic analysis and association with MEF2A-polymorphisms

Assessing the role of TUBA4A gene in frontotemporal degeneration

Lack of association between protocadherin 11-X/Y ( PCDH11X and PCDH11Y ) polymorphisms and late onset Alzheimer's disease

Mutational spectrum of the SPG4 (SPAST) and SPG3A (ATL1) genes in Spanish patients with hereditary spastic paraplegia

No differential DNA methylation of PARK2 in brain of Parkinson's disease patients and healthy controls

Alpha-synuclein transcript isoforms in three different brain regions from Parkinson's disease and healthy subjects in relation to the SNCA rs356165/rs11931074 polymorphisms

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