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Special Issue "Molecular and Genetic Aspects of SARS-CoV-2 Infection and COVID-19 Disease"

International journal of molecular sciences, 2024-05, Vol.25 (9), p.4670

2024

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Brain signal intensity changes as biomarkers in amyotrophic lateral sclerosis

Acta neurologica Scandinavica, 2018-02, Vol.137 (2), p.262-271

2018

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CRIDECO Anticholinergic Load Scale: An Updated Anticholinergic Burden Scale. Comparison with the ACB Scale in Spanish Individuals with Subjective Memory Complaints

Journal of personalized medicine, 2022-02, Vol.12 (2), p.207

2022

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Pharmacist-Physician Interprofessional Collaboration to Promote Early Detection of Cognitive Impairment: Increasing Diagnosis Rate

Frontiers in pharmacology, 2021-04, Vol.12, p.579489-579489

2021

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Relationship between COVID-19 Pandemic Confinement and Worsening or Onset of Depressive Disorders

Brain sciences, 2023-06, Vol.13 (6), p.899

2023

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Influence of daily life and health profile in subtle cognitive decline of women residing in Spanish religious communities: DeCo religious orders study

Frontiers in public health, 2024-07, Vol.12, p.1395877

2024

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The width of the third ventricle associates with cognition and behaviour in motor neuron disease

Acta neurologica Scandinavica, 2019-02, Vol.139 (2), p.118-127

2019

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Editorial: 10 years of Frontiers in genetics: past discoveries, current challenges and future perspectives

Frontiers in genetics, 2023-05, Vol.14, p.1192071-1192071

2023

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Homocysteine and cognitive impairment in Parkinson's disease: A biochemical, neuroimaging, and genetic study

Movement disorders, 2009-07, Vol.24 (10), p.1437-1444

2009

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Epigenetic Study in Parkinson's Disease: A Pilot Analysis of DNA Methylation in Candidate Genes in Brain

Cells (Basel, Switzerland), 2018-09, Vol.7 (10), p.150

2018

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Phylogenetic and in silico structural analysis of the Parkinson disease-related kinase PINK1

Human mutation, 2011-04, Vol.32 (4), p.369-378

2011

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Presenilin-1 Mutations Are a Cause of Primary Lateral Sclerosis-Like Syndrome

Frontiers in molecular neuroscience, 2021-08, Vol.14, p.721047-721047

2021

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Regional distribution of the leucine-rich glioma inactivated ( LGI ) gene family transcripts in the adult mouse brain

Brain research, 2010-01, Vol.1307, p.177-194

2010

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Genetic and constitutional factors are major contributors to substantia nigra hyperechogenicity

Scientific reports, 2017-08, Vol.7 (1), p.7119-9, Article 7119

2017

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LRRK2 is expressed in areas affected by Parkinson's disease in the adult mouse brain

The European journal of neuroscience, 2006-02, Vol.23 (3), p.659-666

2006

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Functional characterization of three single-nucleotide polymorphisms present in the human APOE promoter sequence: Differential effects in neuronal cells and on DNA-protein interactions

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2010-01, Vol.153B (1), p.185-201

2010

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Changes in Liver Lipidomic Profile in G2019S- LRRK2 Mouse Model of Parkinson's Disease

Cells (Basel, Switzerland), 2023-03, Vol.12 (5), p.806

2023

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Other Proteins Involved in Parkinson's Disease and Related Disorders

Current protein & peptide science, 2017-01, Vol.18 (7), p.765-778

2017

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Metabolic alterations in plasma from patients with familial and idiopathic Parkinson's disease

Aging (Albany, NY.), 2020-09, Vol.12 (17), p.16690-16708

2020

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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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The Discovery of the Dardarin Gene 15 Years Later: A Globalized Local History

Movement disorders, 2020-04, Vol.35 (4), p.708-708

2020

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Special Issue "Molecular and Genetic Aspects of SARS-CoV-2 Infection and COVID-19 Disease"

Epigenome-wide association study of COVID-19 severity with respiratory failure

Brain signal intensity changes as biomarkers in amyotrophic lateral sclerosis

CRIDECO Anticholinergic Load Scale: An Updated Anticholinergic Burden Scale. Comparison with the ACB Scale in Spanish Individuals with Subjective Memory Complaints

Pharmacist-Physician Interprofessional Collaboration to Promote Early Detection of Cognitive Impairment: Increasing Diagnosis Rate

Relationship between COVID-19 Pandemic Confinement and Worsening or Onset of Depressive Disorders

Influence of daily life and health profile in subtle cognitive decline of women residing in Spanish religious communities: DeCo religious orders study

The width of the third ventricle associates with cognition and behaviour in motor neuron disease

Editorial: 10 years of Frontiers in genetics: past discoveries, current challenges and future perspectives

Homocysteine and cognitive impairment in Parkinson's disease: A biochemical, neuroimaging, and genetic study

Epigenetic Study in Parkinson's Disease: A Pilot Analysis of DNA Methylation in Candidate Genes in Brain

Phylogenetic and in silico structural analysis of the Parkinson disease-related kinase PINK1

Presenilin-1 Mutations Are a Cause of Primary Lateral Sclerosis-Like Syndrome

Regional distribution of the leucine-rich glioma inactivated ( LGI ) gene family transcripts in the adult mouse brain

Genetic and constitutional factors are major contributors to substantia nigra hyperechogenicity

LRRK2 is expressed in areas affected by Parkinson's disease in the adult mouse brain

Functional characterization of three single-nucleotide polymorphisms present in the human APOE promoter sequence: Differential effects in neuronal cells and on DNA-protein interactions

Rare variants in calcium homeostasis modulator 1 (CALHM1) found in early onset Alzheimer's disease patients alter calcium homeostasis

Changes in Liver Lipidomic Profile in G2019S- LRRK2 Mouse Model of Parkinson's Disease

Other Proteins Involved in Parkinson's Disease and Related Disorders

Metabolic alterations in plasma from patients with familial and idiopathic Parkinson's disease

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 screening of Alzheimer's disease genes in Iberian and African samples yields novel mutations in presenilins and APP

The Discovery of the Dardarin Gene 15 Years Later: A Globalized Local History

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