Lena Obeidova

Prague, PR, Czech Republic

Last Updated: 09/26/2026

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Found 12 publications

Monogenic forms of Parkinson's disease: a Czech cohort study.

Monogenic forms of Parkinson's disease: a Czech cohort study.

Journal: Neurologia i neurochirurgia polska

Published: October 21, 2025

Certain heterozygous variants in the kinase domain of the serine/threonine kinase NEK8 can cause an autosomal dominant form of polycystic kidney disease.

Certain heterozygous variants in the kinase domain of the serine/threonine kinase NEK8 can cause an autosomal dominant form of polycystic kidney disease.

Journal: Kidney international

Published: July 29, 2022

Improvement of Diagnostic Yield by an Additional Amplicon Module to Hybridization-Based Next-Generation Sequencing Panels.

Improvement of Diagnostic Yield by an Additional Amplicon Module to Hybridization-Based Next-Generation Sequencing Panels.

Journal: The Journal of molecular diagnostics : JMD

Published: February 27, 2022

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

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

Journal: Journal of hypertension

Published: January 26, 2022

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

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

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

Journal: Neoplasma

Published: July 31, 2018

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

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

Journal: BMC nephrology

Published: May 22, 2017

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

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

Journal: BMC medical genetics

Published: May 13, 2015

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

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

Journal: BMC medical genetics

Published: August 13, 2013

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

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

Journal: Folia biologica

Published: July 30, 2013

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

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

Journal: Folia biologica

Published: September 18, 2012

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

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

Journal: Folia biologica

Published: May 15, 2012

Showing 1-12 of 12

Last Updated: 09/26/2026