Monica Ceol

Padova, Italy

Last Updated: 09/26/2026

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Found 23 publications

Protein endocytosis dysfunction in kidney biopsies of patients with diabetic nephropathy and minimal change disease: a pilot study on ClC-5 and the megalin receptor.

Protein endocytosis dysfunction in kidney biopsies of patients with diabetic nephropathy and minimal change disease: a pilot study on ClC-5 and the megalin receptor.

Journal: Journal of nephrology

Published: July 30, 2025

Dual-Genetic Etiology in an Atypical Dent Disease Phenotype Which Combines Features of Focal Segmental Glomerulosclerosis and Ellis-Van Creveld-Like Syndrome: A Case Report.

Dual-Genetic Etiology in an Atypical Dent Disease Phenotype Which Combines Features of Focal Segmental Glomerulosclerosis and Ellis-Van Creveld-Like Syndrome: A Case Report.

Journal: Case reports in nephrology and dialysis

Published: July 10, 2025

Human parietal epithelial cells as Trojan horses in albumin overload.

Human parietal epithelial cells as Trojan horses in albumin overload.

Journal: Scientific reports

Published: March 18, 2024

From pollakiuria to Donnai-Barrow syndrome diagnosis in pediatric age.

From pollakiuria to Donnai-Barrow syndrome diagnosis in pediatric age.

Journal: Clinical genetics

Published: April 23, 2023

Human parietal epithelial cells (PECs) and proteinuria in lupus nephritis: a role for ClC-5, megalin, and cubilin?

Human parietal epithelial cells (PECs) and proteinuria in lupus nephritis: a role for ClC-5, megalin, and cubilin?

Journal: Journal of nephrology

Published: January 24, 2023

Emerging Perspectives on the Rare Tubulopathy Dent Disease: Is Glomerular Damage a Direct Consequence of ClC-5 Dysfunction?

Emerging Perspectives on the Rare Tubulopathy Dent Disease: Is Glomerular Damage a Direct Consequence of ClC-5 Dysfunction?

Journal: International journal of molecular sciences

Published: November 23, 2022

Genotype Phenotype Correlation in Dent Disease 2 and Review of the Literature: OCRL Gene Pleiotropism or Extreme Phenotypic Variability of Lowe Syndrome?

Genotype Phenotype Correlation in Dent Disease 2 and Review of the Literature: OCRL Gene Pleiotropism or Extreme Phenotypic Variability of Lowe Syndrome?

Journal: Genes

Published: September 01, 2021

Downregulation of megalin, cubilin, ClC-5 and podocin in Fabry nephropathy: potential implications in the decreased effectiveness of enzyme replacement therapy.

Downregulation of megalin, cubilin, ClC-5 and podocin in Fabry nephropathy: potential implications in the decreased effectiveness of enzyme replacement therapy.

Journal: Journal of nephrology

Published: June 22, 2020

From protein uptake to Dent disease: An overview of the CLCN5 gene.

From protein uptake to Dent disease: An overview of the CLCN5 gene.

Journal: Gene

Published: February 14, 2020

CLCN5 5'UTR isoforms in human kidneys: differential expression analysis between controls and patients with glomerulonephritis.

CLCN5 5'UTR isoforms in human kidneys: differential expression analysis between controls and patients with glomerulonephritis.

Journal: Journal of investigative medicine : the official publication of the American Federation for Clinical Research

Published: January 03, 2020

Genetic Analyses in Dent Disease and Characterization of CLCN5 Mutations in Kidney Biopsies.

Genetic Analyses in Dent Disease and Characterization of CLCN5 Mutations in Kidney Biopsies.

Journal: International journal of molecular sciences

Published: December 04, 2019

Cell Death in the Kidney.

Cell Death in the Kidney.

Journal: International journal of molecular sciences

Published: May 31, 2019

Showing 1-12 of 23

Last Updated: 09/26/2026