Suchergebnisse - "Gianesello, Lisa"

PubPharm (44)

1

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

enthalten in: Journal of nephrology | 2023

von Ceol, M. | Gianesello, L. | Trimarchi, H. | +8

2

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

enthalten in: International journal of molecular sciences | 2023

von Priante, G. | Ceol, M. | Gianesello, L. | +5

3

Rare genetic tubulopathies Gitelman's and Bartter's syndromes and their naturally occurring protection from COVID-19

enthalten in: Minerva medica | 2022

von Sgarabotto, L. | Gianesello, L. | Bertoldi, G. | +3

4

The Lesson Learned from the New c.2547-1G > T Mutation Combined with p.R854Q : When a Type 2N Mutation Reveals a Quantitative von Willebrand Factor Defect

enthalten in: Thrombosis and haemostasis | 2022

von Casonato, A. | Cozzi, M. | Ferrari, S. | +4

5

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

enthalten in: Genes | 2021

von Gianesello, L. | Arroyo, J. | Del Prete, D. | +5

6

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

enthalten in: Journal of nephrology | 2021

von Trimarchi, H. | Ceol, M. | Gianesello, L. | +3

7

Genetics and phenotypic heterogeneity of Dent disease : the dark side of the moon

enthalten in: Human genetics | 2021

von Gianesello, L. | Del Prete, D. | Anglani, F. | +1

8

ACE2 and SARS-CoV-2 Infection Risk : Insights From Patients With Two Rare Genetic Tubulopathies, Gitelman's and Bartter's Syndromes

enthalten in: Frontiers in medicine | 2021

von Calò, L. | Rigato, M. | Sgarabotto, L. | +4

9

Protein uptake at glomerular level : is it just the work of podocytes?

enthalten in: Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association | 2020

von Gianesello, L. | Anglani, F. | Del Prete, D.

10

Genetics and phenotypic heterogeneity of Dent disease: the dark side of the moon

enthalten in: Human genetics | 2020

von Gianesello, L. | Del Prete, D. | Anglani, F. | +1

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