Publications in collaboration with researchers from Hospital Universitario 12 de Octubre (25)

2021

  1. 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

  2. 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

  3. Epidemiology of ataxia and hereditary spastic paraplegia in Spain: a cross-sectional study

    Neurologia

2020

  1. Pre-existing Hemagglutinin Stalk Antibodies Correlate with Protection of Lower Respiratory Symptoms in Flu-Infected Transplant Patients

    Cell Reports Medicine, Vol. 1, Núm. 8

  2. Inborn errors of type I IFN immunity in patients with life-threatening COVID-19

    Science, Vol. 370, Núm. 6515

  3. Autoantibodies against type I IFNs in patients with life-threatening COVID-19

    Science, Vol. 370, Núm. 6515

2019

  1. Neurological disorders in central Spain, second survey: Feasibility pilot observational study

    Journal of Medical Internet Research, Vol. 21, Núm. 1

  2. Deciphering predictive factors for choice of thrombopoietin receptor agonist, treatment free responses, and thrombotic events in immune thrombocytopenia

    Scientific Reports, Vol. 9, Núm. 1

2018

  1. 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

  1. Use of eltrombopag for secondary immune thrombocytopenia in clinical practice

    British Journal of Haematology, Vol. 178, Núm. 6, pp. 959-970

  2. Parkinson's disease severity at 3 years can be predicted from non-motor symptoms at baseline

    Frontiers in Neurology, Vol. 8, Núm. OCT

2016

  1. Heme Oxygenase-1 and 2 Common Genetic Variants and Risk for Multiple Sclerosis

    Scientific Reports, Vol. 6

2015

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

    Brain

  2. 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

  1. 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

  1. 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

  2. Clinical correlates of apathy in patients recently diagnosed with parkinson's disease: The ANIMO Study

    Neuroepidemiology, Vol. 38, Núm. 1, pp. 48-55

2011

  1. Validation of screening instruments for neuroepidemiological surveys of tic disorders

    Movement Disorders, Vol. 26, Núm. 3, pp. 520-526

  2. Tremor in school-aged children: A cross-sectional study of tremor in 819 boys and girls in Burgos, Spain

    Neuroepidemiology, Vol. 37, Núm. 2, pp. 90-95

  3. Prevalence of tics in schoolchildren in central Spain: A population-based study

    Pediatric Neurology, Vol. 45, Núm. 2, pp. 100-108