UNIOVI-PEDIATRIA
OVIPED
Instituto de Investigación Sanitaria del Principado de Asturias
Oviedo, EspañaPublicaciones en colaboración con investigadores/as de Instituto de Investigación Sanitaria del Principado de Asturias (42)
2024
2023
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Age-dependent effect of the IFIH1/MDA5 gene variants on the risk of critical COVID-19
Immunogenetics, Vol. 75, Núm. 2, pp. 91-98
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Chromosome Y Haplogroup R Was Associated with the Risk of Premature Myocardial Infarction with ST-Elevation: Data from the CholeSTEMI Registry
Journal of Clinical Medicine, Vol. 12, Núm. 14
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Clinical Evaluation of Patients with Genetically Confirmed Familial Hypercholesterolemia
Journal of Clinical Medicine, Vol. 12, Núm. 3
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Mitochondrial Heteroplasmy as a Marker for Premature Coronary Artery Disease: Analysis of the Poly-C Tract of the Control Region Sequence
Journal of Clinical Medicine, Vol. 12, Núm. 6
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Nutritional Assessment and Support in Children with Chronic Kidney Disease: The Benefits of Working with a Registered Dietitian
Nutrients, Vol. 15, Núm. 3
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Opportunistic Genetic Screening for Familial Hypercholesterolemia in Heart Transplant Patients
Journal of Clinical Medicine, Vol. 12, Núm. 3
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The IFIH1/MDA5 rs1990760 Gene Variant (946Thr) Differentiates Early- vs. Late-Onset Skin Disease and Increases the Risk of Arthritis in a Spanish Cohort of Psoriasis
International Journal of Molecular Sciences, Vol. 24, Núm. 19
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Transcriptomic clustering of critically ill COVID-19 patients
The European respiratory journal, Vol. 61, Núm. 1
2022
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Association of the Genetic Variation in the Long Non‐Coding RNA FENDRR with the Risk of Developing Hypertrophic Cardiomyopathy
Life, Vol. 12, Núm. 6
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Cellular and Molecular Alterations Underlying Abnormal Bone Growth in X-Linked Hypophosphatemia
International Journal of Molecular Sciences, Vol. 23, Núm. 2
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Common mitochondrial haplogroups as modifiers of the onset-age for critical COVID-19
Mitochondrion, Vol. 67, pp. 1-5
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Different Phenotypes in Monozygotic Twins, Carriers of the Same Pathogenic Variant for Hypertrophic Cardiomyopathy
Life, Vol. 12, Núm. 9
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Effects of IFIH1 rs1990760 variants on systemic inflammation and outcome in critically ill COVID-19 patients in an observational translational study
eLife, Vol. 11
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Emergence of New SARS-CoV2 Omicron Variants after the Change of Surveillance and Control Strategy
Microorganisms, Vol. 10, Núm. 10
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Evaluation of urinary acidification in children: Clinical utility
Frontiers in Pediatrics
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FURIN gene variants (rs6224/rs4702) as potential markers of death and cardiovascular traits in severe COVID-19
Journal of Medical Virology, Vol. 94, Núm. 8, pp. 3589-3595
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Genetic variants in the NF-κB signaling pathway (NFKB1, NFKBIA, NFKBIZ) and risk of critical outcome among COVID-19 patients
Human Immunology, Vol. 83, Núm. 8-9, pp. 613-617
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Hereditary angioedema caused by a novel intronic variant of SERPING1
Pediatric Allergy and Immunology