María José
Currás Tuala
Publicacións (29) Publicacións de María José Currás Tuala
2024
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Host gene expression signatures to identify infection type and organ dysfunction in children evaluated for sepsis: a multicentre cohort study
The Lancet Child and Adolescent Health, Vol. 8, Núm. 5, pp. 325-338
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Multi-tissue transcriptomics of a unique monozygotic discordant twin case of severe progressive osseous heteroplasia
Genes and Diseases, Vol. 11, Núm. 3
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Whole exome sequencing identifies new susceptibility candidates underlying community-acquired pneumonia
Genes and Diseases, Vol. 11, Núm. 6
2023
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Adeno-associated virus 2 infection in children with non-A–E hepatitis
Nature, Vol. 617, Núm. 7961, pp. 555-563
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Biobanking and consenting to research: a qualitative thematic analysis of young people’s perspectives in the North East of England
BMC Medical Ethics, Vol. 24, Núm. 1
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Genomic investigations of unexplained acute hepatitis in children
Nature, Vol. 617, Núm. 7961, pp. 564-573
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Impact of infection on proteome-wide glycosylation revealed by distinct signatures for bacterial and viral pathogens
iScience, Vol. 26, Núm. 8
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Relationship between molecular pathogen detection and clinical disease in febrile children across Europe: a multicentre, prospective observational study
The Lancet Regional Health - Europe, Vol. 32
2022
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A multi-tissue study of immune gene expression profiling highlights the key role of the nasal epithelium in COVID-19 severity
Environmental Research, Vol. 210
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Case Report: Everolimus reduced bone turnover markers but showed no clinical benefit in a patient with severe progressive osseous heteroplasia
Frontiers in Pediatrics, Vol. 10
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Guideline adherence in febrile children below 3 months visiting European Emergency Departments: an observational multicenter study
European Journal of Pediatrics, Vol. 181, Núm. 12, pp. 4199-4209
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Role and Diagnostic Performance of Host Epigenome in Respiratory Morbidity after RSV Infection: The EPIRESVi Study
Frontiers in Immunology, Vol. 13
2021
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Case Report: Two Monochorionic Twins With a Critically Different Course of Progressive Osseus Heteroplasia
Frontiers in Pediatrics, Vol. 9
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Corrigendum: Case Report: Two Monochorionic Twins With a Critically Different Course of Progressive Osseous Heteroplasia (Front. Pediatr., (2021), 9, (662669), 10.3389/fped.2021.662669)
Frontiers in Pediatrics
2020
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Association study of genetic polymorphisms in proteins involved in oseltamivir transport, metabolism, and interactions with adverse reactions in Mexican patients with acute respiratory diseases
Pharmacogenomics Journal, Vol. 20, Núm. 4, pp. 613-620
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Host Transcriptomic Response Following Administration of Rotavirus Vaccine in Infants’ Mimics Wild Type Infection
Frontiers in Immunology, Vol. 11
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Increased Serum Levels of sCD14 and sCD163 Indicate a Preponderant Role for Monocytes in COVID-19 Immunopathology
Frontiers in Immunology, Vol. 11
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Rna-seq data-mining allows the discovery of two long non-coding rna biomarkers of viral infection in humans
International Journal of Molecular Sciences, Vol. 21, Núm. 8
2019
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A qPCR expression assay of IFI44L gene differentiates viral from bacterial infections in febrile children
Scientific Reports, Vol. 9, Núm. 1
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Identification of regulatory variants associated with genetic susceptibility to meningococcal disease
Scientific Reports, Vol. 9, Núm. 1