Novel EYA4 variant in Slovak family with late onset autosomal dominant hearing loss: a case report

door Varga, Lukas, Danis, Daniel, Skopkova, Martina, Masindova, Ivica, Slobodova, Zuzana, Demesova, Lucia, Profant, Milan, Gasperikova, Daniela
Gepubliceerd in BMC Med Genet (2019)

Inflammation time-axis in aseptic loosening of total knee arthroplasty: A preliminary study

door Dyskova, Tereza, Kriegova, Eva, Slobodova, Zuzana, Zehnalova, Sarka, Kudelka, Milos, Schneiderova, Petra, Fillerova, Regina, Gallo, Jiri
Gepubliceerd in PLoS One (2019)

Variant c.2158-2A>G in MANBA is an important and frequent cause of hereditary hearing loss and beta-mannosidosis among the Czech and Slovak Roma population- evidence for a new ethn...

door Safka Brozkova, Dana, Varga, Lukas, Uhrova Meszarosova, Anna, Slobodova, Zuzana, Skopkova, Martina, Soltysova, Andrea, Ficek, Andrej, Jencik, Jan, Lastuvkova, Jana, Gasperikova, Daniela, Seeman, Pavel
Gepubliceerd in Orphanet J Rare Dis (2020)