Anna Uhrova-Meszarosova
5PUBLICATIONS
25CO-AUTHORS
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Publications (5)
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|Jun 30, 2025
Reanalysis of Next-Generation Sequencing Data to Detect Tandem Repeat Expansions in 1,106 Czech Probands With Neurologic Disease.Alena Musilova, Petra Lassuthova, Anna Uhrova Meszarosova
|Jan 23, 2023
A progressive KY myopathy could be caused by a missense pathogenic variant.Anna Uhrova-Meszarosova, Marketa Vlckova, Ladislava Rennerova
|Aug 30, 2020
Spectrum and frequencies of non GJB2 gene mutations in Czech patients with early non-syndromic hearing loss detected by gene panel NGS and whole-exome sequencing.Dana Safka Brozkova, Simona Poisson Marková, Anna Uhrová Mészárosová
|May 20, 2020
Expanding the phenotype spectrum associated with pathogenic variants in the COL2A1 and COL11A1 genes.Jana Čopíková, Jana Paděrová, Věra Románková
|Jul 25, 2017
Disease-Causing Variants in the ATL1 Gene Are a Rare Cause of Hereditary Spastic Paraplegia among Czech Patients.Anna Uhrová Mészárosová, Dagmar Grečmalová, Michaela Brázdilová
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Frequent Collaborators
3 joint publications
Dana Safka-Brozkova
1 joint publications
Jana Čopíková
1 joint publications
Jana Paděrová
1 joint publications
Věra Románková
1 joint publications
Markéta Havlovicová
1 joint publications
Miroslava Balaščáková
1 joint publications
Michaela Zelinová
1 joint publications
Šárka Vejvalková
1 joint publications
Martina Simandlová
1 joint publications
Jana Štěpánková
