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Ana Fakin

Showing results (11-20 of 48) with videos related to

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International Journal of Molecular Sciences|July 9, 2022
The Clinical Spectrum and Disease Course of DRAM2 RetinopathyTjaša Krašovec, Marija Volk, Maja Šuštar Habjan, et al.
Radiology and Oncology|April 12, 2022
Various clinical presentations of uveitis associated with durvalumab treatmentNika Vrabic, Ana Fakin, Polona Jaki Mekjavic, et al.
International Journal of Molecular Sciences|March 6, 2021
Stationary and Progressive Phenotypes Caused by the p.G90D Mutation in Rhodopsin GeneNina Kobal, Tjaša Krašovec, Maja Šuštar, et al.
Acta Ophthalmologica|October 25, 2016
Clinical and genetic heterogeneity in Slovenian patients with BEST diseaseDamjan Glavač, Martina Jarc-Vidmar, Katarina Vrabec, et al.
Genes|February 25, 2023
Stargardt-like Clinical Characteristics and Disease Course Associated with Variants in the <i>WDR19</i> GeneJana Sajovic, Andrej Meglič, Marija Volk, et al.
Retinal Cases & Brief Reports|November 12, 2020
DISRUPTION OF THE OUTER SEGMENTS OF THE PHOTORECEPTORS ON OPTICAL COHERENCE TOMOGRAPHY AS A FEATURE OF VITAMIN A DEFICIENCYKristina Jevnikar, Maja Šuštar, Nada Rotovnik Kozjek, et al.
Ophthalmic Genetics|February 10, 2025
Pathogenic variants in the <i>IFT140</i> gene and an intriguing clinical presentation in two pediatric patients. Cases report and review of literatureMaša Koce, Ana Fakin, Špela Markelj, et al.
Genes|December 11, 2019
Clinical and Haplotypic Variability of Slovenian <i>USH2A</i> Patients Homozygous for the c. 11864G>A Nonsense MutationAndrej Zupan, Ana Fakin, Saba Battelino, et al.
Genes|July 29, 2023
Natural History of Stargardt Disease: The Longest Follow-Up Cohort StudyJana Sajovic, Andrej Meglič, Ana Fakin, et al.
Journal of Clinical Medicine|January 26, 2024
Face Recognition Characteristics in Patients with Age-Related Macular Degeneration Determined Using a Virtual Reality Headset with Eye TrackingNina Žugelj, Lara Peterlin, Urša Muznik, et al.
Pageof 5

Showing results (11-20 of 48) with videos related to

Sort By:
Pageof 5
International Journal of Molecular Sciences|July 9, 2022
The Clinical Spectrum and Disease Course of DRAM2 RetinopathyTjaša Krašovec, Marija Volk, Maja Šuštar Habjan, et al.
Radiology and Oncology|April 12, 2022
Various clinical presentations of uveitis associated with durvalumab treatmentNika Vrabic, Ana Fakin, Polona Jaki Mekjavic, et al.
International Journal of Molecular Sciences|March 6, 2021
Stationary and Progressive Phenotypes Caused by the p.G90D Mutation in Rhodopsin GeneNina Kobal, Tjaša Krašovec, Maja Šuštar, et al.
Acta Ophthalmologica|October 25, 2016
Clinical and genetic heterogeneity in Slovenian patients with BEST diseaseDamjan Glavač, Martina Jarc-Vidmar, Katarina Vrabec, et al.
Genes|February 25, 2023
Stargardt-like Clinical Characteristics and Disease Course Associated with Variants in the <i>WDR19</i> GeneJana Sajovic, Andrej Meglič, Marija Volk, et al.
Retinal Cases & Brief Reports|November 12, 2020
DISRUPTION OF THE OUTER SEGMENTS OF THE PHOTORECEPTORS ON OPTICAL COHERENCE TOMOGRAPHY AS A FEATURE OF VITAMIN A DEFICIENCYKristina Jevnikar, Maja Šuštar, Nada Rotovnik Kozjek, et al.
Ophthalmic Genetics|February 10, 2025
Pathogenic variants in the <i>IFT140</i> gene and an intriguing clinical presentation in two pediatric patients. Cases report and review of literatureMaša Koce, Ana Fakin, Špela Markelj, et al.
Genes|December 11, 2019
Clinical and Haplotypic Variability of Slovenian <i>USH2A</i> Patients Homozygous for the c. 11864G>A Nonsense MutationAndrej Zupan, Ana Fakin, Saba Battelino, et al.
Genes|July 29, 2023
Natural History of Stargardt Disease: The Longest Follow-Up Cohort StudyJana Sajovic, Andrej Meglič, Ana Fakin, et al.
Journal of Clinical Medicine|January 26, 2024
Face Recognition Characteristics in Patients with Age-Related Macular Degeneration Determined Using a Virtual Reality Headset with Eye TrackingNina Žugelj, Lara Peterlin, Urša Muznik, et al.
Pageof 5