Aída Elizabeth
Córdoba Lanús
Researcher in the period 2019-2022
Félix
Claverie Martín
Publications by the researcher in collaboration with Félix Claverie Martín (8)
2023
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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
2020
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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
2018
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URAT1 and GLUT9 mutations in Spanish patients with renal hypouricemia
Clinica Chimica Acta, Vol. 481, pp. 83-89
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
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
2013
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Claudin-19 Mutations and Clinical Phenotype in Spanish Patients with Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis
PLoS ONE, Vol. 8, Núm. 1
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Dent’s disease: Identification of seven new pathogenic mutations in the CLCN5 gene
Journal of Pediatric Genetics, Vol. 2, Núm. 3, pp. 133-140