J. Štekrová

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.

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.

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.

Ambulatory blood pressure and hypertension control in children with autosomal recessive polycystic kidney disease: clinical experience from two central European tertiary centres

J. Štekrová, T. Seeman, L. Obeidová, 2022, Journal of hypertension.

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

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

Hereditary Renal Hypouricemia Type 1 and Autosomal Dominant Polycystic Kidney Disease

J. Štekrová, Makiko Nakamura, B. Stibůrková, 2015, The American journal of the medical sciences.

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.

Two Czech patients with familial adenomatous polyposis presenting mosaicism in APC gene.

J. Štekrová, J. Kotlas, K. Hirschfeldova, 2019, Neoplasma.

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.

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.

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

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

Synchronous gastric and sebaceous cancers, a rare manifestation of MLH1-related Muir-Torre syndrome.

J. Štekrová, V. Mandys, P. Vodicka, 2014, International journal of clinical and experimental pathology.

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.

Cryptic chromosomal rearrangements in children with idiopathic mental retardation in the Czech population.

J. Štekrová, V. Kebrdlová, K. Hirschfeldova, 2011, Genetic testing and molecular biomarkers.

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.

SHOX gene defects and selected dysmorphic signs in patients of idiopathic short stature and Léri-Weill dyschondrosteosis.

R. Gaillyová, J. Štekrová, V. Kebrdlová, 2012, Gene.

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.

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.

Mutational Analysis of the NPHS2 Gene in Czech Patients with Idiopathic Nephrotic Syndrome (nephroticsyndrome/NPHS2gene/focalsegmentalglomerulosclerosis/mutation/polymorphism)

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

Genetic basis of nephrotic syndrome--review.

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

Gitelman syndrome as a cause of psychomotor retardation in a toddler.

J. Štekrová, S. Skálová, P. Lněnička, 2013, Arab journal of nephrology and transplantation.

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 .

Genotype–phenotype correlation in children with autosomal dominant polycystic kidney disease

J. Štekrová, T. Seeman, J. Janda, 2009, Pediatric Nephrology.

Mutation analysis of the MYH gene in unrelated Czech APC mutation-negative polyposis patients.

J. Štekrová, V. Kebrdlová, K. Zídková, 2007, European journal of cancer.

Novel APC mutations in Czech and Slovak FAP families: clinical and genetic aspects

D. Ilencikova, J. Štekrová, V. Kebrdlová, 2007, BMC Medical Genetics.

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.

Molecular analysis of the APC and MYH genes in Czech families affected by FAP or multiple adenomas: 13 novel mutations

J. Štekrová, V. Kebrdlová, J. Vandrovcova, 2004, Human mutation.

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.

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

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

Novel mutations of the APC gene and genetic consequences of splicing mutations in the Czech FAP families

J. Štekrová, V. Kebrdlová, J. Kotlas, 2013, Familial Cancer.

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

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

APC germline mutations identified in Czech patients with familial adenomatous polyposis

J. Štekrová, V. Jirásek, M. Kohoutová, 2002, Human mutation.

Detection of SHOX gene aberrations in routine diagnostic practice and evaluation of phenotype scoring form effectiveness

J. Štekrová, V. Kebrdlová, K. Hirschfeldova, 2016, Journal of Human Genetics.

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

D. Maixnerova, J. Reiterová, J. Štekrová, 2012, Folia biologica.