M. Meliska

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.

M. Michaelides, M. Tesařová, T. Honzík, 2019, Folia biologica.

Clinical and genetic determinants of chronic visual pathway changes after methanol - induced optic neuropathy: four-year follow-up study

L. Vojtová, J. Hubacek, J. Bydžovský, 2018, Clinical toxicology.

Progressive Chronic Retinal Axonal Loss Following Acute Methanol-induced Optic Neuropathy: Four-Year Prospective Cohort Study.

J. Bydžovský, O. Nurieva, D. Pelclova, 2018, American journal of ophthalmology.

Paraproteinemic keratopathy associated with monoclonal gammopathy of undetermined significance (MGUS): clinical findings in twelve patients including recurrence after keratoplasty

S. Tuft, T. Stopka, P. Lišková, 2019, Acta ophthalmologica.

TREATMENT OPTIONS FOR PREMACULAR AND SUB-INTERNAL LIMITING MEMBRANE HEMORRHAGE.

J. Dusková, B. Kalvodová, M. Fichtl, 2021, Ceska a slovenska oftalmologie : casopis Ceske oftalmologicke spolecnosti a Slovenske oftalmologicke spolecnosti.

Peripapillary microcirculation in Leber hereditary optic neuropathy

M. Votruba, J. Bydžovský, T. Honzík, 2018, Acta ophthalmologica.

OCT Findings and Long-term Follow-up Results of Vitrectomy in Patients with Optic Disc Pit and Associated Maculopathy.

B. Kalvodová, M. Kováčová, M. Meliska, 2019, Ceska a slovenska oftalmologie : casopis Ceske oftalmologicke spolecnosti a Slovenske oftalmologicke spolecnosti.

Pigmentary retinopathy can indicate the presence of pathogenic LAMP2 variants even in somatic mosaic carriers with no additional signs of Danon disease

T. Kalina, M. Michaelides, H. Langrová, 2020, Acta ophthalmologica.

Disease-Causing TIMP3 Variants and Deep Phenotyping of Two Czech Families with Sorsby Fundus Dystrophy Associated with Novel p.(Tyr152Cys) Mutation

L. Dudakova, M. Vajter, B. Kousal, 2024, International journal of molecular sciences.