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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.Pediatric Nephrology (Berlin, Germany)|January 22, 2013
Hereditary causes of kidney stones and chronic kidney diseaseVidar O Edvardsson, David S Goldfarb, John C Lieske, et al.Genes|October 23, 2021
Genotype Phenotype Correlation in Dent Disease 2 and Review of the Literature: OCRL Gene Pleiotropism or Extreme Phenotypic Variability of Lowe Syndrome?Lisa Gianesello, Jennifer Arroyo, Dorella Del Prete, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|April 9, 2005
An unusual association of contralateral congenital small kidney, reduced renal function and hyperparathyroidism in sponge kidney patients: on the track of the molecular basisGiovanni Gambaro, Antonia Fabris, Lorenzo Citron, et al.European Journal of Endocrinology|June 12, 2004
Quantitave and qualitative changes in vascular endothelial growth factor gene expression in glomeruli of patients with type 2 diabetesElena Bortoloso, Dorella Del Prete, Michele Dalla Vestra, 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.Kidney International Reports|June 7, 2023
The Site and Type ofMuhammad G Arnous, Jennifer Arroyo, Andrea G Cogal, 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.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.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.Pageof 6