Franca Anglani
Padova, Italy
Last Updated: 09/26/2026
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Found 43 publications
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.
Journal: Scientific reports
Published: March 18, 2024
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?
Journal: Journal of nephrology
Published: January 24, 2023
The Site and Type of CLCN5 Genetic Variation Impact the Resulting Dent Disease-1 Phenotype.
Journal: Kidney international reports
Published: December 22, 2022
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?
Journal: Genes
Published: September 01, 2021
Genotype-phenotype correlation in Gordon's syndrome: report of two cases carrying novel heterozygous mutations.
Journal: Journal of nephrology
Published: February 24, 2021
Two unusual cases of Gitelman's syndrome with a complex inheritance: how the phenotype can help interpret the genotype: lesson for the clinical nephrologist.
Journal: Journal of nephrology
Published: July 02, 2020
Genetics and phenotypic heterogeneity of Dent disease: the dark side of the moon.
Journal: Human genetics
Published: June 24, 2020
From protein uptake to Dent disease: An overview of the CLCN5 gene.
Journal: Gene
Published: February 14, 2020
Last Updated: 09/26/2026