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Comparison of visual requirements and regulations for obtaining a driving license in different European countries and some open questions on their adequacy

Frontiers in human neuroscience, 2022-09, Vol.16, p.927712-927712

2022

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Characterization of Different Types of Epiretinal Proliferations by Synchrotron Radiation-Based Fourier Transform Infrared Micro-Spectroscopy

International journal of molecular sciences, 2023-03, Vol.24 (5), p.4834

2023

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Electroretinography as a Biomarker to Monitor the Progression of Stargardt Disease

International journal of molecular sciences, 2022-12, Vol.23 (24), p.16161

2022

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Polymodal Sensory Transduction in Mouse Corneal Epithelial Cells

Investigative ophthalmology & visual science, 2020-04, Vol.61 (4), p.2

2020

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The Role of Vitamin A in Retinal Diseases

International journal of molecular sciences, 2022-01, Vol.23 (3), p.1014

2022

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ISCEV standard for clinical pattern electroretinography (PERG): 2012 update

Documenta ophthalmologica, 2013-02, Vol.126 (1), p.1-7

2013

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Autologous neurosensory free-flap retinal transplantation for refractory chronic macular hole—outcomes evaluated by OCT, microperimetry, and multifocal electroretinography

Graefe's archive for clinical and experimental ophthalmology, 2021-06, Vol.259 (6), p.1443-1453

2021

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Natural Disease Course in Usher Syndrome Patients Harboring USH2A Variant p.Cys870 in Exon 13, Amenable to Exon Skipping Therapy

Genes, 2023-03, Vol.14 (3), p.652

2023

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UV Effect on Human Anterior Lens Capsule Macro-Molecular Composition Studied by Synchrotron-Based FTIR Micro-Spectroscopy

International journal of molecular sciences, 2021-05, Vol.22 (10), p.5249

2021

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Correlation between the Serum Concentration of Vitamin A and Disease Severity in Patients Carrying p.G90D in RHO , the Most Frequent Gene Associated with Dominant Retinitis Pigmentosa: Implications for Therapy with Vitamin A

International journal of molecular sciences, 2023-01, Vol.24 (1), p.780

2023

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Genetic Characteristics and Long-Term Follow-Up of Slovenian Patients with RPGR Retinal Dystrophy

International journal of molecular sciences, 2023-02, Vol.24 (4), p.3840

2023

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Stationary and Progressive Phenotypes Caused by the p.G90D Mutation in Rhodopsin Gene

International journal of molecular sciences, 2021-02, Vol.22 (4), p.2133

2021

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The Clinical Spectrum and Disease Course of DRAM2 Retinopathy

International journal of molecular sciences, 2022-07, Vol.23 (13), p.7398

2022

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The Analysis of Intracellular and Intercellular Calcium Signaling in Human Anterior Lens Capsule Epithelial Cells with Regard to Different Types and Stages of the Cataract

PloS one, 2015-12, Vol.10 (12), p.e0143781-e0143781

2015

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Popravki avtorjev

Zdravniški vestnik (Ljubljana, Slovenia : 1992), 2021-06, Vol.90 (5-6), p.360-360

2021

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Characteristics of Retinitis Pigmentosa Associated with ADGRV1 and Comparison with USH2A in Patients from a Multicentric Usher Syndrome Study Treatrush

International journal of molecular sciences, 2021-09, Vol.22 (19), p.10352

2021

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Cataract Progression Associated with Modifications in Calcium Signaling in Human Lens Epithelia as Studied by Mechanical Stimulation

Life (Basel, Switzerland), 2021-04, Vol.11 (5), p.369

2021

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Clinical and Histopathological Features of Gelsolin Amyloidosis Associated with a Novel GSN Variant p.Glu580Lys

International journal of molecular sciences, 2021-01, Vol.22 (3), p.1084

2021

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Structural Characteristics of the Lens in Presenile Cataract

Frontiers in medicine, 2021-12, Vol.8, p.802275-802275

2021

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Klinično elektrofiziološko testiranje vida

Zdravniški vestnik (Ljubljana, Slovenia : 1992), 2020-09, Vol.89 (7-8), p.378-397

2020

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Oxidative Stress in Antibiotic Toxic Optic Neuropathy Mimicking Acute LHON in a Patient with Exacerbation of Cystic Fibrosis

Stresses, 2023-03, Vol.3 (1), p.387-396

2023

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Stargardt-like Clinical Characteristics and Disease Course Associated with Variants in the WDR19 Gene

Genes, 2023-01, Vol.14 (2), p.291

2023

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Vision training with VEP biofeedback in amblyopia after the critical period

Documenta ophthalmologica, 2020-12, Vol.141 (3), p.269-278

2020

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Case report: Long-term follow-up of two patients with LHON caused by DNAJC30:c.152G>A pathogenic variant-case series

Frontiers in neurology, 2022-10, Vol.13

2022

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Leber Hereditary Optic Neuropathy (LHON) in Patients with Presumed Childhood Monocular Amblyopia

Journal of clinical medicine, 2023-10, Vol.12 (20), p.6669

2023

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Comparison of visual requirements and regulations for obtaining a driving license in different European countries and some open questions on their adequacy

Characterization of Different Types of Epiretinal Proliferations by Synchrotron Radiation-Based Fourier Transform Infrared Micro-Spectroscopy

Electroretinography as a Biomarker to Monitor the Progression of Stargardt Disease

Polymodal Sensory Transduction in Mouse Corneal Epithelial Cells

The Role of Vitamin A in Retinal Diseases

ISCEV standard for clinical pattern electroretinography (PERG): 2012 update

Autologous neurosensory free-flap retinal transplantation for refractory chronic macular hole—outcomes evaluated by OCT, microperimetry, and multifocal electroretinography

Natural Disease Course in Usher Syndrome Patients Harboring USH2A Variant p.Cys870 in Exon 13, Amenable to Exon Skipping Therapy

UV Effect on Human Anterior Lens Capsule Macro-Molecular Composition Studied by Synchrotron-Based FTIR Micro-Spectroscopy

Correlation between the Serum Concentration of Vitamin A and Disease Severity in Patients Carrying p.G90D in RHO , the Most Frequent Gene Associated with Dominant Retinitis Pigmentosa: Implications for Therapy with Vitamin A

Genetic Characteristics and Long-Term Follow-Up of Slovenian Patients with RPGR Retinal Dystrophy

Stationary and Progressive Phenotypes Caused by the p.G90D Mutation in Rhodopsin Gene

The Clinical Spectrum and Disease Course of DRAM2 Retinopathy

The Analysis of Intracellular and Intercellular Calcium Signaling in Human Anterior Lens Capsule Epithelial Cells with Regard to Different Types and Stages of the Cataract

Popravki avtorjev

Characteristics of Retinitis Pigmentosa Associated with ADGRV1 and Comparison with USH2A in Patients from a Multicentric Usher Syndrome Study Treatrush

Cataract Progression Associated with Modifications in Calcium Signaling in Human Lens Epithelia as Studied by Mechanical Stimulation

Clinical and Histopathological Features of Gelsolin Amyloidosis Associated with a Novel GSN Variant p.Glu580Lys

Structural Characteristics of the Lens in Presenile Cataract

Klinično elektrofiziološko testiranje vida

Oxidative Stress in Antibiotic Toxic Optic Neuropathy Mimicking Acute LHON in a Patient with Exacerbation of Cystic Fibrosis

Stargardt-like Clinical Characteristics and Disease Course Associated with Variants in the WDR19 Gene

Vision training with VEP biofeedback in amblyopia after the critical period

Case report: Long-term follow-up of two patients with LHON caused by DNAJC30:c.152G>A pathogenic variant-case series

Leber Hereditary Optic Neuropathy (LHON) in Patients with Presumed Childhood Monocular Amblyopia

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