Aída Elizabeth
Córdoba Lanús
Researcher in the period 2019-2022
Hospital Universitario Nuestra Señora de Candelaria
Santa Cruz de Tenerife, EspañaPublications in collaboration with researchers from Hospital Universitario Nuestra Señora de Candelaria (39)
2024
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VEGFC Gene Expression Is Associated with Tumor Progression and Disease-Free Survival in Cutaneous Squamous Cell Carcinoma
International Journal of Molecular Sciences, Vol. 25, Núm. 1
2023
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Circulating miR-206 and miR-1246 as Markers in the Early Diagnosis of Lung Cancer in Patients with Chronic Obstructive Pulmonary Disease
International Journal of Molecular Sciences, Vol. 24, Núm. 15
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Expression of angiogenic and lymphangiogenic genes in primary cutaneous melanoma: relationship with angiolymphatic invasion and disease-free survival
Melanoma research, Vol. 33, Núm. 5, pp. 375-387
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Pathogenic Variants of SLC22A12 (URAT1) and SLC2A9 (GLUT9) in Spanish Patients with Renal Hypouricemia: Founder Effect of SLC2A9 Variant c.374C>T; p.(T125M)
International Journal of Molecular Sciences, Vol. 24, Núm. 9
2022
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Gout associated with reduced renal excretion of uric acid. Renal tubular disorder that nephrologists do not treat
Nefrologia, Vol. 42, Núm. 3, pp. 273-279
2021
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Gene Expression Studies in Formalin-Fixed Paraffin-Embedded Samples of Cutaneous Cancer: The Need for Reference Genes
Current issues in molecular biology, Vol. 43, Núm. 3, pp. 2167-2176
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Metformin: Experimental and clinical evidence for a potential role in emphysema treatment
American Journal of Respiratory and Critical Care Medicine, Vol. 204, Núm. 6, pp. 651-666
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Telomere length dynamics over 10-years and related outcomes in patients with COPD
Respiratory Research, Vol. 22, Núm. 1
2020
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Circulating mir-1246 in the progression of chronic obstructive pulmonary disease (Copd) in patients from the bode cohort
International Journal of COPD, Vol. 15, pp. 2727-2737
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Considerations about the molecular basis of some kidney tubule disorders in relation to inbreeding and population displacement
Nefrologia, Vol. 40, Núm. 2, pp. 126-132
2019
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Plasma metabolomics and clinical predictors of survival differences in COPD patients
Respiratory Research, Vol. 20, Núm. 1
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Role of genetic susceptibility in nicotine addiction and chronic obstructive pulmonary disease
Revista de Investigacion Clinica, Vol. 71, Núm. 1, pp. 36-54
2018
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Shorter telomeres in non-smoking patients with airflow limitation
Respiratory Medicine, Vol. 138, pp. 123-128
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URAT1 and GLUT9 mutations in Spanish patients with renal hypouricemia
Clinica Chimica Acta, Vol. 481, pp. 83-89
2017
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Erratum: Telomere shortening and accelerated aging in COPD: Findings from the BODE cohort [Respiratory Research. 59, 1, (2017)(18)] DOI: 10.1186/s12931-017-0547-4
Respiratory Research
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Telomere shortening and accelerated aging in COPD: findings from the BODE cohort
Respiratory research, Vol. 18, Núm. 1, pp. 59
2016
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Prevalence of URAT1 allelic variants in the Roma population
Nucleosides, Nucleotides and Nucleic Acids, Vol. 35, Núm. 10-12, pp. 529-535
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Role of HIF1A, VEGFA and VEGFR2 SNPs in the susceptibility and progression of COPD in a Spanish population
PLoS ONE, Vol. 11, Núm. 5
2015
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Haplotype analysis of CLDN19 single nucleotide polymorphisms in Spanish patients with familial hypomagnesemia with hypercalciuria and nephrocalcinosis
World Journal of Pediatrics, Vol. 11, Núm. 3, pp. 272-275
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IL-8 gene variants are associated with lung function decline and multidimensional BODE index in COPD patients but not with disease susceptibility: A validation study
COPD: Journal of Chronic Obstructive Pulmonary Disease, Vol. 12, Núm. 1, pp. 55-61