UNIOVI-PEDIATRIA
OVIPED
Hospital Universitario Central de Asturias
Oviedo, EspañaPublicaciones en colaboración con investigadores/as de Hospital Universitario Central de Asturias (451)
2024
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An update on clinical presentation and responses to therapy of patients with hereditary hypophosphatemic rickets with hypercalciuria (HHRH)
Kidney International, Vol. 105, Núm. 5, pp. 1058-1076
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Benign acute myositis: Aetiology, treatment and evolution. Five-year experience at a tertiary hospital
Acta Paediatrica, International Journal of Paediatrics
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Chromosome-Y haplogroups in Asturias (Northern Spain) and their association with severe COVID-19
Molecular Genetics and Genomics, Vol. 299, Núm. 1
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Immunoglobulin genes and severity of COVID-19
Immunogenetics, Vol. 76, Núm. 3, pp. 213-217
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Influence of the HLA-Cw6 Allele and IFIH1/MDA5 Gene Variants on the Cardiometabolic Risk Profile of Patients with Psoriatic Disease
Journal of Clinical Medicine, Vol. 13, Núm. 3
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NFKB1 variants were associated with the risk of Parkinson´s disease in male
Journal of Neural Transmission
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New challenges in specialized health training related to skills in telemedicine and information and communication technologies
Educacion Medica
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Retrospective variant reclassification and resequencing in hypertrophic cardiomyopathy: a reference unit centre experience
European Journal of Preventive Cardiology, Vol. 31, Núm. 6, pp. e38-e41
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Survival analysis and gender differences in hypertrophic cardiomyopathy proband patients referred for genetic testing
International Journal of Cardiology, Vol. 408
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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Blocking FGF23 signaling improves the growth plate of mice with X-linked hypophosphatemia
The Journal of endocrinology, Vol. 259, Núm. 1
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Burosumab for X-linked hypophosphatemia in children and adolescents: Opinion based on early experience in seven European countries
Frontiers in Endocrinology, Vol. 13
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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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Intravenous fluid therapy
Pediatric Research
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Is collagen X marker (CXM) a useful index of growth velocity in children with chronic kidney disease?
Pediatric Nephrology
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Long-term complications of primary distal renal tubular acidosis
Pediatric Nephrology, Vol. 38, Núm. 3, pp. 635-642
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Mineral Metabolism in Children: Interrelation between Vitamin D and FGF23
International Journal of Molecular Sciences, Vol. 24, Núm. 7
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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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Neonatal Growth, Nutrition, and Neurodevelopment: A Complex Relationship
Nutrients