Anka Ćurić

发表

Long-Term Functional Hyperemia after Uncomplicated Phacoemulsification: Benefits beyond Restoring Vision

M. Bjeloš, M. Bušić, B. Kuzmanović Elabjer, 2022, Diagnostics.

Corneal Fourier and Belin-Ambrósio Enhanced Ectasia Analysis in Healthy 4-Year-Old White Children.

Dunja Bajtl, M. Bjeloš, M. Bušić, 2023, Cornea.

The First Homozygote Mutation c.499G>T (Asp167Tyr) in the RPE65 Gene Encoding Retinoid Isomerohydrolase Causing Retinal Dystrophy

M. Bjeloš, M. Bušić, B. Kuzmanović Elabjer, 2022, Current issues in molecular biology.

RPE65 c.353G>A, p.(Arg118Lys): A Novel Point Mutation Associated with Retinitis Pigmentosa and Macular Atrophy

D. Bosnar, M. Bjeloš, M. Bušić, 2022, International journal of molecular sciences.

Re: Xiao et al.: Randomized controlled trial of a dichoptic digital therapeutic for amblyopia (Ophthalmology. 2022;129:77-85).

Z. Sonicki, M. Bjeloš, M. Bušić, 2022, Ophthalmology.

Pathogenicity reclassification of the RPE65 c.1580A>G (p.His527Arg) - a case report

D. Bosnar, M. Bjeloš, M. Bušić, 2022, Ophthalmic genetics.

Novel Variant IMPDH1 c.134A>G, p.(Tyr45Cys): Phenotype–Genotype Correlation Revealed Likely Benign Clinical Significance

M. Bjeloš, M. Bušić, Leon Marković, 2023, International journal of molecular sciences.

RPE65 c.393T>A, p.(Asn131Lys): Novel Sequence Variant Detected

D. Bosnar, M. Bjeloš, M. Bušić, 2022, Case reports in ophthalmological medicine.

Vitreous hyper-reflective dots and the macular thickness after cataract surgery

D. Bosnar, T. Georgi, Wolfgang List, 2024, PloS one.

Genotype–Phenotype Correlation Model for the Spectrum of TYR-Associated Albinism

M. Bjeloš, M. Bušić, B. Kuzmanović Elabjer, 2024, Diagnostics.