Investigation unit
Service
Hospital Vall d'Hebron
Barcelona, EspañaPublications in collaboration with researchers from Hospital Vall d'Hebron (21)
2023
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Patients With High Cardiovascular Risk as Candidates to Bempedoic Acid, After Treatment With Statins, Ezetimibe and PCSK9 Inhibitors: An Estimation and Cost-Effectiveness Analysis
Journal of cardiovascular pharmacology, Vol. 81, Núm. 1, pp. 70-75
2022
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Association of rhinitis with asthma prevalence and severity
Scientific Reports, Vol. 12, Núm. 1
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Constipation Predicts Cognitive Decline in Parkinson's Disease: Results from the COPPADIS Cohort at 2-Year Follow-up and Comparison with a Control Group
Journal of Parkinson's Disease, Vol. 12, Núm. 1, pp. 315-331
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Impact of SARS-Cov-2 infection in patients with hypertrophic cardiomyopathy: results of an international multicentre registry
ESC Heart Failure, Vol. 9, Núm. 4, pp. 2189-2198
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Predictors of the change in burden, strain, mood, and quality of life among caregivers of Parkinson's disease patients
International Journal of Geriatric Psychiatry, Vol. 37, Núm. 6
2021
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A multicenter case–control study of the effect of e-nos VNTR polymorphism on upper gastrointestinal hemorrhage in NSAID users
Scientific Reports, Vol. 11, Núm. 1
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Incidence, diagnosis, and outcome of immune-mediated thrombotic thrombocytopenic purpura: A nationwide survey by the Spanish registry of thrombotic thrombocytopenic purpura
Journal of Clinical Apheresis, Vol. 36, Núm. 4, pp. 563-573
2020
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Impaired proteasome activity and neurodegeneration with brain iron accumulation in FBXO7 defect
Annals of Clinical and Translational Neurology, Vol. 7, Núm. 8, pp. 1436-1442
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Online education about end-of-life care and the donation process after brain death and circulatory death. Can we influence perception and attitudes in critical care doctors? A prospective study
Transplant International, Vol. 33, Núm. 11, pp. 1529-1540
2018
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A Novel Heterozygous Intronic Mutation in the FBN1 Gene Contributes to FBN1 RNA Missplicing Events in the Marfan Syndrome
BioMed Research International, Vol. 2018
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Formin Homology 2 Domain Containing 3 (FHOD3) Is a Genetic Basis for Hypertrophic Cardiomyopathy
Journal of the American College of Cardiology, Vol. 72, Núm. 20, pp. 2457-2467
2017
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Assessment of plasma chitotriosidase activity, CCL18/PARC concentration and NP-C suspicion index in the diagnosis of Niemann-Pick disease type C: A prospective observational study
Journal of Translational Medicine, Vol. 15, Núm. 1
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Cross-sectional study about impact of parental smoking on rhinitis symptoms in children
Clinical Otolaryngology, Vol. 42, Núm. 6, pp. 1275-1280
2015
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Inter-laboratory evaluation of instrument platforms and experimental workflows for quantitative accuracy and reproducibility assessment
EuPA Open Proteomics, Vol. 8, pp. 6-15
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Manejo de la sedación y la analgesia en unidades de cuidados intensivos neonatales españolas
Anales de Pediatria, Vol. 83, Núm. 2, pp. 75-84
2014
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Lack of replication of higher genetic risk load in men than in women with systemic lupus erythematosus
Arthritis Research and Therapy, Vol. 16, Núm. 3
2012
2010
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Association study of the serotoninergic system in migraine in the Spanish population
American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, Vol. 153, Núm. 1, pp. 177-184
2009
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Replication of recently identified systemic lupus erythematosus genetic associations: A case-control study
Arthritis Research and Therapy, Vol. 11, Núm. 3
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Two-stage case-control association study of dopamine-related genes and migraine
BMC Medical Genetics, Vol. 10, pp. 95