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Purification of Vero cell derived live replication deficient influenza A and B virus by ion exchange monolith chromatography

Vaccine, 2014-05, Vol.32 (21), p.2487-2492

2014

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Separation of pegylated recombinant proteins and isoforms on CIM ion exchangers

Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2016-10, Vol.1033-1034, p.91-96

2016

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Comparison of Alkaline Lysis with Electroextraction and Optimization of Electric Pulses to Extract Plasmid DNA from Escherichia coli

The Journal of membrane biology, 2013-11, Vol.246 (11), p.861-867

2013

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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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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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Natural History of Stargardt Disease: The Longest Follow-Up Cohort Study

Genes, 2023-07, Vol.14 (7), p.1394

2023

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Stargardt-like Clinical Characteristics and Disease Course Associated with Variants in the IWDR19/I Gene

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

2023

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Electrophysiological and SD-OCT findings in patients receiving chloroquine therapy in relation to cumulative dosage and duration of treatment

Documenta ophthalmologica, 2020-08, Vol.141 (1), p.1-14

2020

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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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Disease Progression in CNGA3 and CNGB3 Retinopathy; Characteristics of Slovenian Cohort and Proposed OCT Staging Based on Pooled Data from 126 Patients from 7 Studies

Current issues in molecular biology, 2021-08, Vol.43 (2), p.941-957

2021

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ABCA4 Variant c.5714+5G>A in Trans With Null Alleles Results in Primary RPE Damage

Investigative ophthalmology & visual science, 2023-09, Vol.64 (12), p.33-33

2023

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Clinical and Haplotypic Variability of Slovenian USH2A Patients Homozygous for the c. 11864G>A Nonsense Mutation

Genes, 2019-12, Vol.10 (12), p.1015

2019

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Leberjeva hereditarna optična nevropatija – pregled bolezni z analizo prisotnosti v Sloveniji

Zdravniški vestnik (Ljubljana, Slovenia : 1992), 2022-10, Vol.91 (9-10), p.1-14

2022

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Fundus autofluorescence and optical coherence tomography in relation to visual function in Usher syndrome type 1 and 2

Vision research (Oxford), 2012-12, Vol.75 (9), p.60-70

2012

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Cone Dystrophy Associated with a Novel Variant in the Terminal Codon of the RPGR - ORF15

Genes, 2021-03, Vol.12 (4), p.499

2021

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Clinical and genetic heterogeneity in Slovenian patients with BEST disease

Acta ophthalmologica (Oxford, England), 2016-12, Vol.94 (8), p.e786-e794

2016

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The Relative Preservation of the Central Retinal Layers in Leber Hereditary Optic Neuropathy

Journal of clinical medicine, 2022-10, Vol.11 (20), p.6045

2022

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Double Hyperautofluorescent Rings in Patients with USH2A-Retinopathy

Genes, 2019-11, Vol.10 (12), p.956

2019

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Abnormal fundus autofluorescence in relation to retinal function in patients with retinitis pigmentosa

Graefe's archive for clinical and experimental ophthalmology, 2005-10, Vol.243 (10), p.1018-1027

2005

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Morphological and functional parameters in X-linked retinoschisis patients-A multicentre retrospective cohort study

Frontiers in medicine, 2024-01, Vol.10, p.1331889-1331889

2024

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An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients

European journal of human genetics : EJHG, 2016-12, Vol.24 (12), p.1730-1738

2016

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Clinical and electrophysiology findings in Slovene patients with Leber hereditary optic neuropathy

Documenta ophthalmologica, 2015-06, Vol.130 (3), p.179-187

2015

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Morphology and function of the retina in children and young adults with Stargardt dystrophy

Zdravniški vestnik (Ljubljana, Slovenia : 1992), 2012-01, Vol.81

2012

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Purification of Vero cell derived live replication deficient influenza A and B virus by ion exchange monolith chromatography

Separation of pegylated recombinant proteins and isoforms on CIM ion exchangers

Comparison of Alkaline Lysis with Electroextraction and Optimization of Electric Pulses to Extract Plasmid DNA from Escherichia coli

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

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

Natural History of Stargardt Disease: The Longest Follow-Up Cohort Study

Stargardt-like Clinical Characteristics and Disease Course Associated with Variants in the IWDR19/I Gene

Electrophysiological and SD-OCT findings in patients receiving chloroquine therapy in relation to cumulative dosage and duration of treatment

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

Disease Progression in CNGA3 and CNGB3 Retinopathy; Characteristics of Slovenian Cohort and Proposed OCT Staging Based on Pooled Data from 126 Patients from 7 Studies

ABCA4 Variant c.5714+5G>A in Trans With Null Alleles Results in Primary RPE Damage

Clinical and Haplotypic Variability of Slovenian USH2A Patients Homozygous for the c. 11864G>A Nonsense Mutation

Leberjeva hereditarna optična nevropatija – pregled bolezni z analizo prisotnosti v Sloveniji

Fundus autofluorescence and optical coherence tomography in relation to visual function in Usher syndrome type 1 and 2

Cone Dystrophy Associated with a Novel Variant in the Terminal Codon of the RPGR - ORF15

Clinical and genetic heterogeneity in Slovenian patients with BEST disease

The Relative Preservation of the Central Retinal Layers in Leber Hereditary Optic Neuropathy

Double Hyperautofluorescent Rings in Patients with USH2A-Retinopathy

Abnormal fundus autofluorescence in relation to retinal function in patients with retinitis pigmentosa

Morphological and functional parameters in X-linked retinoschisis patients-A multicentre retrospective cohort study

An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients

Clinical and electrophysiology findings in Slovene patients with Leber hereditary optic neuropathy

Morphology and function of the retina in children and young adults with Stargardt dystrophy

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