Giovanni Piscopo

Bari, 70124, Italy

Last Updated: 09/26/2026

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Found 13 publications

Peritoneal dialysis-associated peritonitis in two patients with Bartter syndrome and end-stage kidney disease: a case report.

Peritoneal dialysis-associated peritonitis in two patients with Bartter syndrome and end-stage kidney disease: a case report.

Journal: Kidney & blood pressure research

Published: March 31, 2026

Estimation of Kidney Volumes in Autosomal Dominant Polycystic Kidney Disease: A Comparison Between Manual Segmentation and Ellipsoid Formula.

Estimation of Kidney Volumes in Autosomal Dominant Polycystic Kidney Disease: A Comparison Between Manual Segmentation and Ellipsoid Formula.

Journal: Clinics and practice

Published: September 01, 2025

Urinary epidermal growth factor/monocyte chemotactic peptide 1 ratio as non-invasive predictor of Mayo clinic imaging classes in autosomal dominant polycystic kidney disease.

Urinary epidermal growth factor/monocyte chemotactic peptide 1 ratio as non-invasive predictor of Mayo clinic imaging classes in autosomal dominant polycystic kidney disease.

Journal: Journal of nephrology

Published: April 21, 2022

Therapeutic Approach for Recurrent Focal Segmental Glomerulosclerosis in Pediatric Renal Transplant Recipients: A Single-Center Experience.

Therapeutic Approach for Recurrent Focal Segmental Glomerulosclerosis in Pediatric Renal Transplant Recipients: A Single-Center Experience.

Journal: Blood purification

Published: May 11, 2021

Peripheral nervous system manifestations of Shiga toxin-producing E. coli-induced haemolytic uremic syndrome in children.

Peripheral nervous system manifestations of Shiga toxin-producing E. coli-induced haemolytic uremic syndrome in children.

Journal: Italian journal of pediatrics

Published: February 14, 2021

Low C3 Serum Levels Predict Severe Forms of STEC-HUS With Neurologic Involvement.

Low C3 Serum Levels Predict Severe Forms of STEC-HUS With Neurologic Involvement.

Journal: Frontiers in medicine

Published: May 04, 2020

Mid-Aortic Syndrome: A Rare Cause of Renovascular Hypertension in Childhood Treated Percutaneously with an Unusual Vascular Access.

Mid-Aortic Syndrome: A Rare Cause of Renovascular Hypertension in Childhood Treated Percutaneously with an Unusual Vascular Access.

Journal: Current pediatric reviews

Published: March 16, 2020

Practical approach to patient therapy affected by Autosomal Dominant Autosomic Polycystic Kidney Disease

Practical approach to patient therapy affected by Autosomal Dominant Autosomic Polycystic Kidney Disease

Journal: Giornale italiano di nefrologia : organo ufficiale della Societa italiana di nefrologia

Published: July 24, 2018

Von Hippel-Lindau disease: when neurosurgery meets nephrology, ophthalmology and genetics.

Von Hippel-Lindau disease: when neurosurgery meets nephrology, ophthalmology and genetics.

Journal: Journal of neurosurgical sciences

Published: July 28, 2017

Clinical Manifestations in Autosomal Dominant Polycystic Kidney Disease (ADPKD)

Clinical Manifestations in Autosomal Dominant Polycystic Kidney Disease (ADPKD)

Journal: Giornale italiano di nefrologia : organo ufficiale della Societa italiana di nefrologia

Published: November 01, 2016

Renal failure, management of uremic condition and replacement therapy

Renal failure, management of uremic condition and replacement therapy

Journal: Giornale italiano di nefrologia : organo ufficiale della Societa italiana di nefrologia

Published: November 01, 2016

Two rare cases of Acremonium acute endophthalmitis after cataract surgery in a tertiary care hospital.

Two rare cases of Acremonium acute endophthalmitis after cataract surgery in a tertiary care hospital.

Journal: The new microbiologica

Published: May 05, 2013

Showing 1-12 of 13

Last Updated: 09/26/2026