J. Reiterová

发表

The influence of endothelin-A receptor gene polymorphism on the progression of autosomal dominant polycystic kidney disease and IgA nephropathy.

D. Maixnerova, V. Tesar, J. Reiterová, 2007, Folia biologica.

Bilineal inheritance of pathogenic PKD1 and PKD2 variants in a Czech family with autosomal dominant polycystic kidney disease – a case report

V. Tesar, J. Reiterová, M. Merta, 2018, BMC Nephrology.

The retrospective analysis of 343 Czech patients with IgA nephropathy--one centre experience.

D. Maixnerova, V. Tesar, J. Reiterová, 2011, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

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

V. Tesar, J. Reiterová, 2022, International journal of molecular sciences.

Influence of the Alpha-Adducin and ACE Gene Polymorphism on the Progression of Autosomal-Dominant Polycystic Kidney Disease

V. Tesar, J. Reiterová, M. Merta, 2003, Kidney and Blood Pressure Research.

IgA Nephropathy in Czech Patients - Are We Able Reliably Predict the Outcome?

D. Maixnerova, V. Tesar, J. Reiterová, 2014, Kidney and Blood Pressure Research.

The influence of two megsin polymorphisms on the progression of IgA nephropathy.

D. Maixnerova, V. Tesar, J. Reiterová, 2008, Folia biologica.

Autosomal dominant polycystic kidney disease in a family with mosaicism and hypomorphic allele

V. Tesar, J. Reiterová, M. Merta, 2013, BMC Nephrology.

The influence of three endothelin-1 polymorphisms on the progression of IgA nephropathy.

D. Maixnerova, V. Tesar, J. Reiterová, 2007, Folia biologica.

Nationwide biopsy survey of renal diseases in the Czech Republic during the years 1994–2011

D. Maixnerova, V. Tesar, J. Reiterová, 2015, Journal of Nephrology.

The coincidence of IgA nephropathy and Fabry disease

D. Maixnerova, V. Tesar, J. Reiterová, 2013, BMC Nephrology.

The coincidence of IgA nephropathy and

V. Tesar, J. Reiterová, M. Merta, 2013 .

Role of endothelin and nitric oxide in the pathogenesis of arterial hypertension in autosomal dominant polycystic kidney disease.

V. Tesar, T. Zima, J. Reiterová, 2003, Physiological research.

The influence of vascular endothelial growth factor (VEGF) polymorphism on the progression of chronic glomerulonephritides.

D. Maixnerova, V. Tesar, J. Reiterová, 2011, Folia biologica.

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

F. Nevens, C. Ahn, J. Reiterová, 2018, Liver international : official journal of the International Association for the Study of the Liver.

A pilot study conducted in the Czech Republic relating to the molecular analysis of the RET and GDNF genes in patients with cakut, predominantly unilateral renal agenesis

A. Vicha, V. Tesar, J. Reiterová, 2015 .

Long-term outcome of patients with idiopathic membranous nephropathy.

D. Maixnerova, V. Tesar, J. Reiterová, 2006, Prague medical report.

Does electron microscopy change the view of the diagnosis of IgA nephropathy?

D. Maixnerova, V. Tesar, J. Reiterová, 2005, Prague medical report.

Multi-population genome wide association study implicates both immune and non-immune factors in the etiology of pediatric steroid sensitive nephrotic syndrome

V. Tasic, E. Fiaccadori, A. Gharavi, 2022, medRxiv.

Silica and Asbestos Exposure in ANCA-Associated Vasculitis with Pulmonary Involvement

D. Maixnerova, V. Tesar, J. Reiterová, 2005, Renal failure.

Four novel mutations of the PKD2 gene in czech families with autosomal dominant polycystic kidney disease

D. Peters, J. Reiterová, M. Merta, 2002, Human mutation.

A nationwide blood spot screening study for Fabry disease in the Czech Republic haemodialysis patient population.

D. Maixnerova, V. Tesar, J. Reiterová, 2006, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Genetics of diabetic nephropathy.

V. Tesar, J. Reiterová, M. Merta, 2003, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

The Influence of G‐Protein β3‐Subunit Gene and Endothelial Nitric Oxide Synthase Gene in Exon 7 Polymorphisms on Progression of Autosomal Dominant Polycystic Kidney Disease

V. Tesar, J. Reiterová, J. Štekrová, 2004, Renal failure.

Long-Term Outcome of Patients with Antineutrophil Cytoplasmic Autoantibody-Associated Vasculitis with Renal Involvement

V. Tesar, J. Reiterová, M. Merta, 2005, Kidney and Blood Pressure Research.

Secondary Membranous Nephropathy—One Center Experience

V. Tesar, J. Reiterová, M. Merta, 2005, Renal failure.

Mutational Analysis of ACTN 4 , Encoding α-Actinin 4 , in Patients with Focal Segmental Glomerulosclerosis Using HRM Method ( focal segmental glomerulosclerosis / minimal change disease / α-actinin 4 / mutational analysis / / high-resolution melting method )

V. Tesar, J. Reiterová, J. Štekrová, 2013 .

The Influence of the Endothelin-Converting Enzyme-1 Gene Polymorphism on the Progression of Autosomal Dominant Polycystic Kidney Disease

V. Tesar, J. Reiterová, M. Merta, 2006, Renal failure.

Influence of Endothelin-1 Gene Polymorphisms on the Progression of Autosomal Dominant Polycystic Kidney Disease

D. Maixnerova, V. Tesar, J. Reiterová, 2006, Kidney and Blood Pressure Research.

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

M. Rudnicki, A. Tislér, G. Mayer, 2019, Orphanet Journal of Rare Diseases.

Short Communication TRPC6 Gene Variants in Czech Adult Patients with Focal Segmental Glomerulosclerosis and Minimal Change Disease

V. Tesar, J. Reiterová, J. Štekrová, 2012 .

Molecular genetic analysis of PKHD1 by next-generation sequencing in Czech families with autosomal recessive polycystic kidney disease

J. Reiterová, J. Štekrová, T. Seeman, 2015, BMC Medical Genetics.

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

M. Rudnicki, A. Tislér, G. Mayer, 2021, Frontiers in Immunology.

CFHR5 Genetic Variations and Serum Levels in Patients with Immune-Complex-Mediated Membranoproliferative Glomerulonephritis and C3-Glomerulopathy

M. Rudnicki, A. Tislér, J. Reiterová, 2020 .

Novel mutations of PKD genes in the Czech population with autosomal dominant polycystic kidney disease

V. Tesar, J. Reiterová, M. Merta, 2014, BMC Medical Genetics.

DNA analysis of renal electrolyte transporter genes among patients suffering from Bartter and Gitelman syndromes: summary of mutation screening.

J. Reiterová, J. Štekrová, R. Ryšavá, 2011, Folia biologica.

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

V. Tesar, J. Reiterová, J. Štekrová, 2018, BMC Medical Genetics.

New mutations in the PKD1 gene in Czech population with autosomal dominant polycystic kidney disease

J. Reiterová, M. Merta, J. Štekrová, 2009, BMC Medical Genetics.

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

L. Kiemeney, A. Köttgen, I. Ionita-Laza, 2020, Nature Communications.

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

L. Kiemeney, A. Köttgen, I. Ionita-Laza, 2020, Nature Communications.

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

J. Reiterová, J. Štekrová, T. Seeman, 2020, PloS one.

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

M. Rudnicki, A. Tislér, G. Mayer, 2019, Clinical kidney journal.

Mutational analysis of the NPHS2 gene in Czech patients with idiopathic nephrotic syndrome.

D. Maixnerova, V. Tesar, J. Reiterová, 2012, Folia biologica.

Current and Future Therapeutical Options in Alport Syndrome

V. Tesar, J. Reiterová, 2023, International journal of molecular sciences.

Genetic basis of nephrotic syndrome--review.

D. Maixnerova, V. Tesar, J. Reiterová, 2006, Prague medical report.

Mutational Analysis of the NPHS 2 Gene in Czech Patients with Idiopathic Nephrotic Syndrome ( nephrotic syndrome / NPHS 2 gene / focal segmental glomerulosclerosis / mutation / polymorphism )

J. Reiterová, M. Merta, J. Štekrová, 2012 .

PKD 1 and PKD 2 mutations in Slovenian families with autosomal dominant polycystic kidney disease

L. Strmečki, J. Reiterová, J. Štekrová, 2006 .

PKD1 and PKD2 mutations in Slovenian families with autosomal dominant polycystic kidney disease

L. Strmečki, J. Reiterová, J. Štekrová, 2006, BMC Medical Genetics.

Mutational analysis of ACTN4, encoding α-actinin 4, in patients with focal segmental glomerulosclerosis using HRM method.

V. Tesar, J. Reiterová, J. Štekrová, 2013, Folia biologica.

TRPC6 gene variants in Czech adult patients with focal segmental glomerulosclerosis and minimal change disease.

V. Tesar, J. Reiterová, J. Štekrová, 2012, Folia biologica.

PKD2 mutations in a Czech population with autosomal dominant polycystic kidney disease.

J. Reiterová, M. Merta, J. Štekrová, 2004, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

PKD 2 mutations in a Czech population with autosomal dominant polycystic kidney disease

J. Damborský, J. Reiterová, M. Merta, 2004 .

Genetic Analysis of Gitelman Syndrome Patients from the Czech Republic and Slovakia – Three Novel Mutations Found

J. Reiterová, M. Merta, J. Štekrová, 2007, Kidney and Blood Pressure Research.

Endothelial Nitric Oxide Synthase Affects the Progression of Autosomal Dominant Polycystic Kidney Disease

V. Tesar, J. Reiterová, M. Merta, 2002, Kidney and Blood Pressure Research.

INFLUENCE OF THE ENDOTHELIAL NITRIC OXIDE SYNTHASE POLYMORPHISM ON THE PROGRESSION OF AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE AND IgA NEPHROPATHY

V. Tesar, J. Reiterová, M. Merta, 2002, Renal failure.

INFLUENCE OF THE ENDOTHELIAL NITRIC OXIDE SYNTHASE POLYMORPHISM ON THE PROGRESSION OF AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE AND IgA NEPHROPATHY

V. Tesar, J. Reiterová, M. Merta, 2002, Renal failure.

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

S. Raychaudhuri, V. Tasic, R. Loos, 2023, Nature communications.

Influence of VEGF Polymorphism on Progression of Autosomal Dominant Polycystic Kidney Disease

D. Maixnerova, V. Tesar, J. Reiterová, 2008, Kidney and Blood Pressure Research.

PKD1 and PKD2 mutations in Slovenian families with autosomal dominant polycystic kidney disease

L. Strmečki, J. Reiterová, J. Štekrová, 2006, BMC Medical Genetics.

Two familial cases of antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis.

V. Tesar, J. Reiterová, E. Jančová, 2006, Rheumatology.