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B Kousal

Showing results (1-10 of 13) with videos related to

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Ceska a Slovenska Oftalmologie : Casopis Ceske Oftalmologicke Spolecnosti a Slovenske Oftalmologicke Spolecnosti|May 12, 2015
[Dynamic vitreomacular traction]P Cigánek, L Matoušková, B Kousal
Ceska a Slovenska Oftalmologie : Casopis Ceske Oftalmologicke Spolecnosti a Slovenske Oftalmologicke Spolecnosti|April 5, 2016
[Clinical Tests Testing New Therapies for Stargardt Disease]B Kousal, Ľ Ďuďáková, L Hlavatá, et al.
Ceska a Slovenska Oftalmologie : Casopis Ceske Oftalmologicke Spolecnosti a Slovenske Oftalmologicke Spolecnosti|September 11, 2020
Innovative strategies for treating retinal diseasesZ Straňák, B Kousal, T Ardan, et al.
Ceska a Slovenska Oftalmologie : Casopis Ceske Oftalmologicke Spolecnosti a Slovenske Oftalmologicke Spolecnosti|November 19, 2016
[Gene Therapy for Inherited RETINAL AND OPTIC NERVE Disorders: Current Knowledge]Ľ Ďuďáková, B Kousal, H Kolářová, et al.
Ceska a Slovenska Oftalmologie : Casopis Ceske Oftalmologicke Spolecnosti a Slovenske Oftalmologicke Spolecnosti|February 3, 2015
[The molecular genetic and clinical findings in two probands with Stargardt disease]B Kousal, J Záhlava, Š Vejvalková, et al.
Ceska a Slovenska Oftalmologie : Casopis Ceske Oftalmologicke Spolecnosti a Slovenske Oftalmologicke Spolecnosti|May 13, 2015
[STORY of the Papilla - a Case Report]A Beňová, P Kuthan, B Kousal, et al.
Ceska a Slovenska Oftalmologie : Casopis Ceske Oftalmologicke Spolecnosti a Slovenske Oftalmologicke Spolecnosti|January 27, 2022
TREATMENT OPTIONS FOR PREMACULAR AND SUB-INTERNAL LIMITING MEMBRANE HEMORRHAGEM Kováčová, B Kousal, M Meliška, et al.
Ceska a Slovenska Oftalmologie : Casopis Ceske Oftalmologicke Spolecnosti a Slovenske Oftalmologicke Spolecnosti|May 14, 2020
Molecular genetic cause of achromatopsia in two patients of Czech originL Hlavatá, Ľ Ďuďáková, J Moravíková, et al.
Ceska a Slovenska Oftalmologie : Casopis Ceske Oftalmologicke Spolecnosti a Slovenske Oftalmologicke Spolecnosti|July 5, 2013
[Clinical findings in members of a Czech family with retinitis pigmentosa caused by the c.2426_2427delAG mutation in RPGR]B Kousal, P Skalická, P Diblík, et al.
Ceska a Slovenska Oftalmologie : Casopis Ceske Oftalmologicke Spolecnosti a Slovenske Oftalmologicke Spolecnosti|March 28, 2012
[Minimal ocular findings in a patient with Best disease caused by the c.653G>A mutation in BEST1]B Kousal, F Chakarova, G C Black, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Ceska a Slovenska Oftalmologie : Casopis Ceske Oftalmologicke Spolecnosti a Slovenske Oftalmologicke Spolecnosti|May 12, 2015
[Dynamic vitreomacular traction]P Cigánek, L Matoušková, B Kousal
Ceska a Slovenska Oftalmologie : Casopis Ceske Oftalmologicke Spolecnosti a Slovenske Oftalmologicke Spolecnosti|April 5, 2016
[Clinical Tests Testing New Therapies for Stargardt Disease]B Kousal, Ľ Ďuďáková, L Hlavatá, et al.
Ceska a Slovenska Oftalmologie : Casopis Ceske Oftalmologicke Spolecnosti a Slovenske Oftalmologicke Spolecnosti|September 11, 2020
Innovative strategies for treating retinal diseasesZ Straňák, B Kousal, T Ardan, et al.
Ceska a Slovenska Oftalmologie : Casopis Ceske Oftalmologicke Spolecnosti a Slovenske Oftalmologicke Spolecnosti|November 19, 2016
[Gene Therapy for Inherited RETINAL AND OPTIC NERVE Disorders: Current Knowledge]Ľ Ďuďáková, B Kousal, H Kolářová, et al.
Ceska a Slovenska Oftalmologie : Casopis Ceske Oftalmologicke Spolecnosti a Slovenske Oftalmologicke Spolecnosti|February 3, 2015
[The molecular genetic and clinical findings in two probands with Stargardt disease]B Kousal, J Záhlava, Š Vejvalková, et al.
Ceska a Slovenska Oftalmologie : Casopis Ceske Oftalmologicke Spolecnosti a Slovenske Oftalmologicke Spolecnosti|May 13, 2015
[STORY of the Papilla - a Case Report]A Beňová, P Kuthan, B Kousal, et al.
Ceska a Slovenska Oftalmologie : Casopis Ceske Oftalmologicke Spolecnosti a Slovenske Oftalmologicke Spolecnosti|January 27, 2022
TREATMENT OPTIONS FOR PREMACULAR AND SUB-INTERNAL LIMITING MEMBRANE HEMORRHAGEM Kováčová, B Kousal, M Meliška, et al.
Ceska a Slovenska Oftalmologie : Casopis Ceske Oftalmologicke Spolecnosti a Slovenske Oftalmologicke Spolecnosti|May 14, 2020
Molecular genetic cause of achromatopsia in two patients of Czech originL Hlavatá, Ľ Ďuďáková, J Moravíková, et al.
Ceska a Slovenska Oftalmologie : Casopis Ceske Oftalmologicke Spolecnosti a Slovenske Oftalmologicke Spolecnosti|July 5, 2013
[Clinical findings in members of a Czech family with retinitis pigmentosa caused by the c.2426_2427delAG mutation in RPGR]B Kousal, P Skalická, P Diblík, et al.
Ceska a Slovenska Oftalmologie : Casopis Ceske Oftalmologicke Spolecnosti a Slovenske Oftalmologicke Spolecnosti|March 28, 2012
[Minimal ocular findings in a patient with Best disease caused by the c.653G>A mutation in BEST1]B Kousal, F Chakarova, G C Black, et al.
Pageof 2