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Biomedical Papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia|June 23, 2021
Modern diagnostic and therapeutic approaches in familial maculopathy with reference to North Carolina macular dystrophyJana Nekolova, Alexandr Stepanov, Bohdan Kousal, et al.Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|March 20, 2018
SD-OCT imaging as a valuable tool to support molecular genetic diagnostics of Usher syndrome type 1Radka Kremlikova Pourova, Jana Paderova, Jana Copikova, et al.Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|April 27, 2016
Phenotypic features of CRB1-associated early-onset severe retinal dystrophy and the different molecular approaches to identifying the disease-causing variantsBohdan Kousal, Lubica Dudakova, Renata Gaillyova, et al.BMC Ophthalmology|June 6, 2021
ALG3-CDG: a patient with novel variants and review of the genetic and ophthalmic findingsMartina Farolfi, Anna Cechova, Nina Ondruskova, et al.Acta Ophthalmologica|September 28, 2018
Peripapillary microcirculation in Leber hereditary optic neuropathyBohdan Kousal, Hana Kolarova, Martin Meliska, et al.Frontiers in Genetics|June 5, 2023
Case report: A rare variant m.4135T>C in theTereza Rákosníková, Silvie Kelifová, Hana Štufková, et al.Genes|November 27, 2021
Clinical and Genetic Study of X-Linked Juvenile Retinoschisis in the Czech PopulationBohdan Kousal, Lucia Hlavata, Hana Vlaskova, et al.International Journal of Molecular Sciences|April 13, 2024
Disease-Causing TIMP3 Variants and Deep Phenotyping of Two Czech Families with Sorsby Fundus Dystrophy Associated with Novel p.(Tyr152Cys) MutationAndrea Vergaro, Monika Pankievic, Jana Jedlickova, et al.Clinical Genetics|June 15, 2023
MIR204 n.37C>T variant as a cause of chorioretinal dystrophy variably associated with iris coloboma, early-onset cataracts and congenital glaucomaJana Jedlickova, Marie Vajter, Tomas Barta, et al.Molecular Vision|October 30, 2014
Severe retinal degeneration in women with a c.2543del mutation in ORF15 of the RPGR geneBohdan Kousal, Pavlina Skalicka, Lucie Valesova, et al.Pageof 2