Patient management – genetic testing and practical considerations
Liskova, P., Kolarova, H., Kousal, B., Honzik, T.
Published in Acta ophthalmologica (Oxford, England) (01.09.2017)
Published in Acta ophthalmologica (Oxford, England) (01.09.2017)
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Journal Article
Genetic causes of deaf‐blindness in sixteen Czech families
Kousal, B., Dudakova, L., Bujakowska, K., Liskova, P.
Published in Acta ophthalmologica (Oxford, England) (01.09.2017)
Published in Acta ophthalmologica (Oxford, England) (01.09.2017)
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Journal Article
Two novel KERA mutations causing cornea plana in a Czech family and associated phenotypes
Skalická, P., Dudakova, L., Liskova, P.
Published in Acta ophthalmologica (Oxford, England) (01.10.2016)
Published in Acta ophthalmologica (Oxford, England) (01.10.2016)
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Journal Article
Molecular genetic basis of Usher syndrome in the Czech population
Liskova, P., Kousal, B., Bujakowska, K., Dudakova, L.
Published in Acta ophthalmologica (Oxford, England) (01.10.2016)
Published in Acta ophthalmologica (Oxford, England) (01.10.2016)
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Journal Article
Phenotype Variability in Czech Patients Carrying PAX6 Disease-Causing Variants
Moravikova, J, Kozmik, Z, Hlavata, L, Putzova, M, Skalicka, P, Michaelides, M, Malinka, F, Dudakova, L, Liskova, P
Published in Folia biologica (01.01.2020)
Published in Folia biologica (01.01.2020)
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Journal Article
Macular corneal dystrophy and associated corneal thinning
Dudakova, L, Palos, M, Svobodova, M, Bydzovsky, J, Huna, L, Jirsova, K, Hardcastle, A J, Tuft, S J, Liskova, P
Published in Eye (London) (01.10.2014)
Published in Eye (London) (01.10.2014)
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Journal Article
OPA1 analysis in an international series of probands with bilateral optic atrophy
Liskova, P., Tesarova, M., Dudakova, L., Stepanka, S., Kolarova, H., Honzik, T., Seto, S., Votruba, M.
Published in Acta ophthalmologica (Oxford, England) (01.10.2016)
Published in Acta ophthalmologica (Oxford, England) (01.10.2016)
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Journal Article
Sequencing of the CHST6 gene in Czech macular corneal dystrophy patients supports the evidence of a founder mutation
Liskova, P, Veraitch, B, Jirsova, K, Filipec, M, Neuwirth, A, Ebenezer, N D, Hysi, P G, Hardcastle, A J, Tuft, S J, Bhattacharya, S S
Published in British journal of ophthalmology (01.02.2008)
Published in British journal of ophthalmology (01.02.2008)
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Journal Article
Review of SRD5A3 Disease-Causing Sequence Variants and Ocular Findings in Steroid 5α-Reductase Type 3 Congenital Disorder of Glycosylation, and a Detailed New Case
Kousal, B, Honzík, T, Hansíková, H, Ondrušková, N, Čechová, A, Tesařová, M, Stránecký, V, Meliška, M, Michaelides, M, Lišková, P
Published in Folia biologica (01.01.2019)
Published in Folia biologica (01.01.2019)
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Journal Article
Treatment with azathioprine and cyclic methylprednisolone has little or no effect on bioactivity in anti-interferon beta antibody-positive patients with multiple sclerosis
Bojar, M, Zajac, M, Meluzínova, E, Houžvičková, E, Libertinová, J, Lišková, P, Mat'oška, V, Nyč, O, Mináriková, M
Published in Multiple sclerosis (01.12.2010)
Published in Multiple sclerosis (01.12.2010)
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Journal Article
Descemet membrane endothelial keratoplasty with a stromal rim (DMEK-S)
Studeny, Pavel, Farkas, Andrej, Vokrojova, Magdalena, Liskova, Petra, Jirsova, Katerina
Published in British journal of ophthalmology (01.07.2010)
Published in British journal of ophthalmology (01.07.2010)
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Journal Article