Publications
- Hearing Function in Heterozygous Carriers of a Pathogenic GJB2 Gene Mutation2013 | Second Faculty of Medicine
- Changes in otoacoustic emissions and high-frequency hearing thresholds in children and adolescents2006 | Second Faculty of Medicine
- Age-related changes in cochlear and brainstem auditory functions in Fischer 344 rats2006 | 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 of mutations in CX 26 gene in 142 patients with congenital nonsyndromic hearing loss2003 | Second Faculty of Medicine, Central Library of Charles University
- Contemporary view of the newborn hearing screening2003 | Second Faculty of Medicine, Central Library of Charles University
- Newborn hearing screening in the University Hospital Motol, Prague2003 | Second Faculty of Medicine, Central Library of Charles University
- Molecular genetic testing in patients with autosomal recessive non syndromic hearing loss and deafness2003 | Second Faculty of Medicine
- Screning for hearing impairment in newborns using transient evoked otoacoustic emissions2003 | Second Faculty of Medicine
- Cochlear function in young and adult Fischer 344 rats2003 | Second Faculty of Medicine
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