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Bioscience Reports|December 7, 2017
Caspase-independent programmed cell death triggers Ca2PO4 deposition in an in vitro model of nephrocalcinosisGiovanna Priante, Federica Quaggio, Lisa Gianesello, et al.
Case Reports in Nephrology and Dialysis|January 2, 2026
Dual-Genetic Etiology in an Atypical Dent Disease Phenotype Which Combines Features of Focal Segmental Glomerulosclerosis and Ellis-Van Creveld-Like Syndrome: A Case ReportDorella Del Prete, Monica Ceol, Alessandra Giannella, et al.
Scientific Reports|October 24, 2017
Albumin uptake in human podocytes: a possible role for the cubilin-amnionless (CUBAM) complexLisa Gianesello, Giovanna Priante, Monica Ceol, et al.
Springerplus|September 22, 2015
Nephrolithiasis, kidney failure and bone disorders in Dent disease patients with and without CLCN5 mutationsFranca Anglani, Angela D'Angelo, Luisa Maria Bertizzolo, et al.
Journal of Cellular and Molecular Medicine|February 19, 2015
Spontaneous calcification process in primary renal cells from a medullary sponge kidney patient harbouring a GDNF mutationFederica Mezzabotta, Rosalba Cristofaro, Monica Ceol, et al.
European Journal of Human Genetics : EJHG|October 11, 2012
An atypical Dent's disease phenotype caused by co-inheritance of mutations at CLCN5 and OCRL genesMaria Addis, Cristiana Meloni, Enrica Tosetto, et al.
Clinical Reviews in Allergy & Immunology|March 26, 2015
PTX3, Anti-PTX3, and Anti-C1q Autoantibodies in Lupus GlomerulonephritisNicola Bassi, Dorella Del Prete, Anna Ghirardello, et al.
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