FACULTAD DE CIENCIAS DE LA SALUD
Facultad/Centro de investigación
Hospital Universitario 12 de Octubre
Madrid, EspañaPublicaciones en colaboración con investigadores/as de Hospital Universitario 12 de Octubre (28)
2023
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A second update on mapping the human genetic architecture of COVID-19
Nature
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Epidemiology of ataxia and hereditary spastic paraplegia in Spain: a cross-sectional study
Neurologia, Vol. 38, Núm. 6, pp. 379-386
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Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19
Genome Medicine, Vol. 15, Núm. 1
2022
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Novel genes and sex differences in COVID-19 severity
Human molecular genetics, Vol. 31, Núm. 22, pp. 3789-3806
2021
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Influence of Genetic Polymorphisms on the Response to Tramadol, Ibuprofen, and the Combination in Patients With Moderate to Severe Pain After Dental Surgery
Clinical Therapeutics, Vol. 43, Núm. 5, pp. e86-e102
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SARS-CoV-2-related MIS-C: A key to the viral and genetic causes of Kawasaki disease?
Journal of Experimental Medicine, Vol. 218, Núm. 6
2020
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Autoantibodies against type I IFNs in patients with life-threatening COVID-19
Science, Vol. 370, Núm. 6515
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Inborn errors of type I IFN immunity in patients with life-threatening COVID-19
Science, Vol. 370, Núm. 6515
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Pre-existing Hemagglutinin Stalk Antibodies Correlate with Protection of Lower Respiratory Symptoms in Flu-Infected Transplant Patients
Cell Reports Medicine, Vol. 1, Núm. 8
2019
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Neurological disorders in central Spain, second survey: Feasibility pilot observational study
Journal of Medical Internet Research, Vol. 21, Núm. 1
2018
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Improvement of impulse control disorders associated with levodopa–carbidopa intestinal gel treatment in advanced Parkinson’s disease
Journal of Neurology, Vol. 265, Núm. 6, pp. 1279-1287
2017
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Parkinson's disease severity at 3 years can be predicted from non-motor symptoms at baseline
Frontiers in Neurology, Vol. 8, Núm. OCT
2016
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Heme Oxygenase-1 and 2 Common Genetic Variants and Risk for Multiple Sclerosis
Scientific Reports, Vol. 6
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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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
2014
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Characterization of the repeat expansion size in C9orf72 in amyotrophic lateral sclerosis and frontotemporal dementia
Human Molecular Genetics, Vol. 23, Núm. 3, pp. 749-754
2012
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Clinical correlates of apathy in patients recently diagnosed with parkinson's disease: The ANIMO Study
Neuroepidemiology, Vol. 38, Núm. 1, pp. 48-55
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Impact of apathy on health-related quality of life in recently diagnosed Parkinson's disease: The ANIMO study
Movement Disorders, Vol. 27, Núm. 2, pp. 211-218
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School Performance in Tic Disorders. A Cross-Sectional Study of School Performance in 1,867 Children in Central Spain (IN10-1.001)
Neurology, Vol. 78, Núm. 1 Supplement
2011
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Prevalence of tics in schoolchildren in central Spain: A population-based study
Pediatric Neurology, Vol. 45, Núm. 2, pp. 100-108