Jana Reiterova

Prague, PR, Czech Republic

Last Updated: 09/26/2026

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Found 30 publications

Czech nationwide screening for Fabry disease in patients on maintenance dialysis: a call for evaluation of population-enriched GLA gene variants of uncertain significance.

Czech nationwide screening for Fabry disease in patients on maintenance dialysis: a call for evaluation of population-enriched GLA gene variants of uncertain significance.

Journal: Clinical kidney journal

Published: December 15, 2024

The most common founder pathogenic variant c.868G > A (p.Val290Met) in the NPHS2 gene in a representative adult Czech cohort with focal segmental glomerulosclerosis is associated with a milder disease and its underdiagnosis in childhood.

The most common founder pathogenic variant c.868G > A (p.Val290Met) in the NPHS2 gene in a representative adult Czech cohort with focal segmental glomerulosclerosis is associated with a milder disease and its underdiagnosis in childhood.

Journal: Frontiers in medicine

Published: October 11, 2023

Current and Future Therapeutical Options in Alport Syndrome.

Current and Future Therapeutical Options in Alport Syndrome.

Journal: International journal of molecular sciences

Published: January 02, 2023

Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome.

Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome.

Journal: Nature communications

Published: September 15, 2022

Autosomal Dominant Polycystic Kidney Disease: From Pathophysiology of Cystogenesis to Advances in the Treatment.

Autosomal Dominant Polycystic Kidney Disease: From Pathophysiology of Cystogenesis to Advances in the Treatment.

Journal: International journal of molecular sciences

Published: February 18, 2022

FHR-5 Serum Levels and CFHR5 Genetic Variations in Patients With Immune Complex-Mediated Membranoproliferative Glomerulonephritis and C3-Glomerulopathy.

FHR-5 Serum Levels and CFHR5 Genetic Variations in Patients With Immune Complex-Mediated Membranoproliferative Glomerulonephritis and C3-Glomerulopathy.

Journal: Frontiers in immunology

Published: June 03, 2021

Results of targeted next-generation sequencing in children with cystic kidney diseases often change the clinical diagnosis.

Results of targeted next-generation sequencing in children with cystic kidney diseases often change the clinical diagnosis.

Journal: PloS one

Published: January 08, 2020

The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis.

The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis.

Journal: Nature communications

Published: August 28, 2019

C4 nephritic factor in patients with immune-complex-mediated membranoproliferative glomerulonephritis and C3-glomerulopathy.

C4 nephritic factor in patients with immune-complex-mediated membranoproliferative glomerulonephritis and C3-glomerulopathy.

Journal: Orphanet journal of rare diseases

Published: July 25, 2019

Validation of distinct pathogenic patterns in a cohort of membranoproliferative glomerulonephritis patients by cluster analysis.

Validation of distinct pathogenic patterns in a cohort of membranoproliferative glomerulonephritis patients by cluster analysis.

Journal: Clinical kidney journal

Published: February 26, 2019

Severity in polycystic liver disease is associated with aetiology and female gender: Results of the International PLD Registry.

Severity in polycystic liver disease is associated with aetiology and female gender: Results of the International PLD Registry.

Journal: Liver international : official journal of the International Association for the Study of the Liver

Published: March 30, 2018

Mutational screening of inverted formin 2 in adult-onset focal segmental glomerulosclerosis or minimal change patients from the Czech Republic.

Mutational screening of inverted formin 2 in adult-onset focal segmental glomerulosclerosis or minimal change patients from the Czech Republic.

Journal: BMC medical genetics

Published: December 20, 2017

Showing 1-12 of 30

Last Updated: 09/26/2026