LEIRE
GONDRA SANGRONIZ
PROFESORADO ASOCIADO
Hospital Universitario de Cruces
Barakaldo, EspañaPublicaciones en colaboración con investigadoras/es de Hospital Universitario de Cruces (6)
2024
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Dilated Cardiomyopathy With Concomitant Salt-Losing Renal Tubulopathy Caused by Heterozygous RRAGD Gene Variant
Circulation: Genomic and Precision Medicine, Vol. 17, Núm. 2, pp. E004336
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Use of rasburicase to improve kidney function in children with hyperuricemia and acute kidney injury
Clinical and Experimental Nephrology, Vol. 28, Núm. 1, pp. 13-22
2023
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Genotypic variability in patients with clinical diagnosis of Bartter syndrome type 3
Scientific reports, Vol. 13, Núm. 1, pp. 12587
2022
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Parathyroid hormone and phosphate homeostasis in patients with Bartter and Gitelman syndrome: an international cross-sectional study
Nephrology Dialysis Transplantation, Vol. 37, Núm. 12, pp. 2474-2486
2021
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Hereditary distal renal tubular acidosis: Genotypic correlation, evolution to long term, and new therapeutic perspectives
Nefrologia, Vol. 41, Núm. 4, pp. 383-390
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Molecular aspects and long-term outcome of patients with primary distal renal tubular acidosis
Pediatric Nephrology, Vol. 36, Núm. 10, pp. 3133-3142