ÓSCAR ERNESTO
ZURRIAGA LLORENS
TITULAR DE UNIVERSIDAD
Centro de Investigación Biomédica en Red sobre Epidemiología Y Salud Pública
Madrid, EspañaPublications en collaboration avec des chercheurs de Centro de Investigación Biomédica en Red sobre Epidemiología Y Salud Pública (48)
2024
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Socioeconomic disparities in changes to preterm birth and stillbirth rates during the first year of the COVID-19 pandemic: a study of 21 European countries
European journal of public health, Vol. 34, Núm. 1, pp. i58-i66
2023
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Causes of death in children with congenital anomalies up to age 10 in eight European countries
BMJ Paediatrics Open, Vol. 7, Núm. 1
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Diagnostic delay in rare diseases: between fear and resilience
Gaceta Sanitaria, Vol. 37
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La enfermedad de Huntington en la Comunitat Valenciana
Revista de neurologia, Vol. 76, Núm. 11, pp. 343-350
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Prevalence of Hereditary Hemorrhagic Telangiectasia: a population-based study in the Valencian region (Spain)
Revista Espanola de Salud Publica, Vol. 97
2022
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Incidence of Kidney Replacement Therapy and Subsequent Outcomes Among Patients With Systemic Lupus Erythematosus: Findings From the ERA Registry
American Journal of Kidney Diseases, Vol. 79, Núm. 5, pp. 635-645
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The ERA Registry Annual Report 2019: Summary and age comparisons
Clinical Kidney Journal, Vol. 15, Núm. 3, pp. 452-472
2021
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Geographical variability in mortality in urban areas: A joint analysis of 16 causes of death
International Journal of Environmental Research and Public Health, Vol. 18, Núm. 11
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The ERA-EDTA Registry Annual Report 2018: A summary
Clinical Kidney Journal, Vol. 14, Núm. 1, pp. 107-123
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Updating of the official statistics of deaths causes: “Let’s get stronger after the COVID-19 pandemic”
Revista Espanola de Salud Publica, Vol. 95
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Wilson's disease in Spain: validation of sources of information used by the Rare Diseases Registries
Gaceta Sanitaria, Vol. 35, Núm. 6, pp. 551-558
2020
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Congenital heart defects in the Valencian Community 2007-2014: The Population-Based Registry Of Congenital Anomalies
Anales de Pediatria, Vol. 92, Núm. 1, pp. 13-20
2019
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Coffee consumption and mortality from all causes of death, cardiovascular disease and cancer in an elderly Spanish population
European Journal of Nutrition, Vol. 58, Núm. 6, pp. 2439-2448
2017
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Drugs use in pregnancy in the Valencia Region and the risk of congenital anomalies
Anales de Pediatria, Vol. 87, Núm. 3, pp. 135-142
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La validez del Conjunto Mínimo Básico de Datos como fuente de identificación de las anomalías congénitas en la Comunitat Valenciana
Gaceta Sanitaria, Vol. 31, Núm. 3, pp. 220-226
2016
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Anomalías cromosómicas: la experiencia del Registro de Anomalías Congénitas de la Comunitat Valenciana
Anales de Pediatria, Vol. 84, Núm. 4, pp. 203-210
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Applying probabilistic temporal and multisite data quality control methods to a public health mortality registry in Spain: A systematic approach to quality control of repositories
Journal of the American Medical Informatics Association, Vol. 23, Núm. 6, pp. 1085-1095
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Consensus on the criteria needed for creating a rare-disease patient registry. A Delphi study
Journal of Public Health (United Kingdom), Vol. 38, Núm. 2, pp. e178-e186
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Corrigendum to "An open heart: Experiences of the parents of children with congenital heartdisease" [Gac Sanit. 2015; 29,(6):445-50] Doi: 10.1016/j.gaceta.2015.07.009
Gaceta Sanitaria
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The changing trends and outcomes in renal replacement therapy: Data from the ERA-EDTA Registry
Nephrology Dialysis Transplantation, Vol. 31, Núm. 5, pp. 831-841