MANUEL
FERNANDEZ MARTINEZ
PROFESORADO AGREGADO
Publikationen (102) Publikationen von MANUEL FERNANDEZ MARTINEZ
2024
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Anti-alpha synuclein and anti-tau immunotherapies: Can a cocktail approach work?
Parkinsonism and Related Disorders, Vol. 122
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DRD4 gene polymorphism and impulse control disorder induced by dopamine agonists in Parkinson's disease
Annals of Clinical and Translational Neurology, Vol. 11, Núm. 8, pp. 2222-2229
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Enhanced quantitation of pathological α-synuclein in patient biospecimens by RT-QuIC seed amplification assays
PLoS Pathogens, Vol. 20, Núm. 9
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Fluid and tissue biomarkers in Parkinson's disease: Immunodetection or seed amplification? Central or peripheral?
Parkinsonism and Related Disorders, Vol. 121
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Mitochondrial DNA deletions in the cerebrospinal fluid of patients with idiopathic REM sleep behaviour disorder
eBioMedicine, Vol. 102
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Sphingosine 1-phosphate receptor subtype 1 (S1P1) activity in the course of Alzheimer's disease
Neurobiology of Disease, Vol. 202
2023
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Altered sleep and neurovascular dysfunction in alpha-synucleinopathies: the perfect storm for glymphatic failure
Frontiers in Aging Neuroscience, Vol. 15
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Midbrain and pons MRI shape analysis and its clinical and CSF correlates in degenerative parkinsonisms: a pilot study
European Radiology, Vol. 33, Núm. 7, pp. 4540-4551
2022
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Cell-free mitochondrial DNA deletions in idiopathic, but not LRRK2, Parkinson's disease
Neurobiology of Disease, Vol. 174
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Combined CSF α-SYN RT-QuIC, CSF NFL and midbrain-pons planimetry in degenerative parkinsonisms: From bedside to bench, and back again
Parkinsonism and Related Disorders, Vol. 99, pp. 33-41
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Development of castration resistance in prostate cancer patients treated with luteinizing hormone-releasing hormone analogues (LHRHa): results of the ANARESISTANCE study
World Journal of Urology, Vol. 40, Núm. 10, pp. 2459-2466
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Differential Phospho-Signatures in Blood Cells Identify LRRK2 G2019S Carriers in Parkinson's Disease
Movement Disorders, Vol. 37, Núm. 5, pp. 1004-1015
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Increased Phospho-AKT in Blood Cells from LRRK2 G2019S Mutation Carriers
Annals of Neurology, Vol. 92, Núm. 5, pp. 888-894
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Serum MicroRNAs Predict Isolated Rapid Eye Movement Sleep Behavior Disorder and Lewy Body Diseases
Movement Disorders, Vol. 37, Núm. 10, pp. 2086-2098
2021
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Cross-sectional associations of cerebrospinal α-synuclein, tau and amyloid-β with dyskinesias, motor fluctuations, non-motor symptoms in a cohort of Parkinson's disease patients
Journal of the Neurological Sciences
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Exome-wide rare variant analysis in familial essential tremor
Parkinsonism and Related Disorders, Vol. 82, pp. 109-116
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Finding genetically-supported drug targets for Parkinson’s disease using Mendelian randomization of the druggable genome
Nature Communications, Vol. 12, Núm. 1
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Human-lineage-specific genomic elements are associated with neurodegenerative disease and APOE transcript usage
Nature Communications, Vol. 12, Núm. 1
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Identification of sixteen novel candidate genes for late onset Parkinson’s disease
Molecular Neurodegeneration, Vol. 16, Núm. 1
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Investigation of Autosomal Genetic Sex Differences in Parkinson's Disease
Annals of Neurology, Vol. 90, Núm. 1, pp. 35-42