ENFERMEDADES RENALES HEREDITARIAS Y RARAS
Vall d'Hebron Institut de Recerca
Barcelona, EspañaPublicaciones en colaboración con investigadores/as de Vall d'Hebron Institut de Recerca (5)
2023
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Clinical and genetic characteristics of Dent's disease type 1 in Europe
Nephrology Dialysis Transplantation, Vol. 38, Núm. 6, pp. 1497-1507
2022
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Induction immunosuppression and outcome in kidney transplant recipients with early COVID-19 after transplantation
Clinical Kidney Journal, Vol. 15, Núm. 11, pp. 2039-2045
2021
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Familial hypomagnesemia with hypercalciuria and nephrocalcinosis
Pediatric Nephrology, Vol. 36, Núm. 10, pp. 3045-3055
2020
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Novel compound heterozygous mutations of CLDN16 in a patient with familial hypomagnesemia with hypercalciuria and nephrocalcinosis
Molecular Genetics and Genomic Medicine, Vol. 8, Núm. 11
2019
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Apolipoprotein A-Ib as a biomarker of focal segmental glomerulosclerosis recurrence after kidney transplantation: diagnostic performance and assessment of its prognostic value – a multi-centre cohort study
Transplant International, Vol. 32, Núm. 3, pp. 313-322