Publications
- Hearing Function in Heterozygous Carriers of a Pathogenic GJB2 Gene Mutation2013 | Second Faculty of Medicine
- Double Heterozygosity with Mutations Involving both the GJB2 and GJB6 Genes is a Possible, but very Rare, Cause of Congenital Deafness in the Czech Population2005 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
- Spectrum and frequencies of mutations in the GJB2 (Cx26) gene among 156 Czech patients with pre-lingual deafness2004 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
- Spectrum of mutations in CX 26 gene in 142 patients with congenital nonsyndromic hearing loss2003 | Second Faculty of Medicine, Central Library of Charles University
- Spectrum of Mutations in the Connexin 26 Gene among 142 Patients with Congenital Deafness in Czech Republic.2003 | Second Faculty of Medicine
- Connnexin 26 in children with cochlear implant2002 | Second Faculty of Medicine, Central Library of Charles University
- Examination ofthe Gene for Connexin 26 in Czech Patients with Congenital Autosomal Recessive Non-SyndromicHearing Loss2002 | Second Faculty of Medicine
- Závratě2017 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport, Third Faculty of Medicine, Faculty of Medicine in Hradec Králové
- Balloon Dilatation of Pediatric Subglottic Laryngeal Stenosis during the Artificial Apneic Pause: Experience in 5 Children2014 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
- Orbitocellulitis and its therapy at the child age2011 | Second Faculty of Medicine
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