- SCA2 trinucleotide expansion in German SCA patients1997 | Second Faculty of Medicine
- Trinucleotide Repeat Expansions and Human Genetic Disease1995 | Central Library of Charles University, Second Faculty of Medicine
- Should Patients with Kearns-Sayre Syndrome and Corneal Endothelial Failure Be Genotyped for a TCF4 Trinucleotide Repeat, Commonly Associated with Fuchs Endothelial Corneal Dystrophy?2021 | First Faculty of Medicine
- Should Patients with Kearns -Sayre Syndrome and Corneal Endothelial Failure Be Genotyped for a TCF4 Trinucleotide Repeat,Commonly Associated with Fuchs Endothelial Corneal Dystrophy2021 | First Faculty of Medicine
- SCA6 is caused by moderate CAG expansion in the alpha(1A)-voltage-dependent calcium channel gene1997 | Second Faculty of Medicine
- Spinocerebellar Ataxias Type 8, 12, and 17 and Dentatorubro-Pallidoluysian Atrophy in Czech Ataxic Patients2013 | First Faculty of Medicine, Central Library of Charles University, Second Faculty of Medicine
- Identification of novel informative loci for DNA-based X-inactivation analysis2015 | First Faculty of Medicine
- NOTCH2NLC CGG Repeats Are Not Expanded and Skin Biopsy Was Negative in an Infantile Patient With Neuronal Intranuclear Inclusion Disease2020 | First Faculty of Medicine, Third Faculty of Medicine, Faculty of Medicine in Pilsen
- Antisense Therapy for a Common Corneal Dystrophy Ameliorates TCF4 Repeat Expansion-Mediated Toxicity2018 | First Faculty of Medicine
- Oculopharyngeal muscular dystrophy in the population of the Czech Republic2013 | Second Faculty of Medicine
- The Number of CAG Repeats Within the Normal Allele Does Not Influence the Age of Onset in Huntington's Disease2011 | First Faculty of Medicine, Faculty of Physical Education and Sport
- Correlation between Relaxometry and Diffusion Tensor Imaging in the Globus Pallidus of Huntington's Disease Patients2015 | First Faculty of Medicine, Central Library of Charles University, Third Faculty of Medicine
- CpG Methylation, a Parent-of-Origin Effect for Maternal-Biased Transmission of Congenital Myotonic Dystrophy2017 | First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
- Highly Unstable Sequence Interruptions of the CTG Repeat in the Myotonic Dystrophy Gene2009 | Second Faculty of Medicine
- Huntington's Disease2010 | First Faculty of Medicine
- Can ataxin-2 be down-regulated by allele-specific de novo DNA methylation in SCA2 patients?2004 | Second Faculty of Medicine
- DNA diagnostics of Friedrich's ataxia1997 | Second Faculty of Medicine
- Genotype/phenotype correlation in a SCA1 family: anticipation without CAG expansion2005 | Second Faculty of Medicine
- Human genome - chromosome X: focused on Xq281995 | Second Faculty of Medicine
- Fluorescent multiplex PCR: Fast method for autosomal dominant spinocerebellar ataxias screening2005 | Second Faculty of Medicine
- Fluorescence-based automated fragment analysis of microsatellite polymorphism within the transmembrane region of the MIC-A gene2004 | Third Faculty of Medicine
- Fluorescence-based automated fragment analysis of microsatellite polymorphism within the transmembrane region of the MIC-A gene2004 | Central Library of Charles University
- Myotonic dystrophies2012 | Second Faculty of Medicine
- Carnosine as a protective factor in diabetic nephropathy: association with a leucine repeat of the carnosinase gene CNDP12005 | Third Faculty of Medicine
- Formation of a Thymine-Hg-II-Thymine Metal-Mediated DNA Base Pair: Proposal and Theoretical Calculation of the Reaction Pathway2013 | Faculty of Mathematics and Physics
- Genetic Study of Twenty Patients with Autism Spectrum Disorders2002 | Second Faculty of Medicine