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Retina September 2023

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

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Jana Sajovic; Andrej Meglič; Zelia Corradi; Mubeen Khan; Aleš Maver; Martina Jarc Vidmar; Marko Hawlina; Frans P. M. Cremers; Ana Fakin
TAGS: abca4 gene, alleles, photoreceptors
Invest. Ophthalmol. Vis. Sci.. 2023; 64(12):33. https://doi.org/10.1167/iovs.64.12.33

Includes: Supplemental Content

ARVO Annual Meeting Abstract June 2022

Relative preservation of central retinal layers in LHON in comparison to other optic neuropathies

Sanja Petrovic Pajic; Luka Lapajne; Ana Fakin; Martina Jarc Vidmar; Damjan Glavač; Marija Volk; Aleš Maver; Bor Vratanar; Janez Stare; Borut Peterlin; Marko Hawlina

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):2603 – F0486.

ARVO Annual Meeting Abstract June 2022

TRPV4 involvement in inflammation and tissue damage in corneal epithelium

Luka Lapajne; Monika Lakk; Marko Hawlina; David Krizaj

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):3244 – A0279.

ARVO Annual Meeting Abstract June 2022

Electroretinography as a biomarker to monitor Stargardt disease

Jana Sajovic; Andrej Meglič; Maja Šuštar Habjan; Marko Hawlina; Ana Fakin

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):3534.

ARVO Annual Meeting Abstract June 2021

Characterisation of Stargardt disease pathogenesis associated with the frequent ABCA4 mutation c.5714+5G>A

Jana Sajovic; Andrej Meglič; Martina Jarc-Vidmar; Frans P.M. Cremers; Mubeen Khan; Zelia Corradi; Claire-Marie Dhaenens; Damjan Glavač; Aleš Maver; Marija Volk; Borut Peterlin; Marko Hawlina; Ana Fakin

Invest. Ophthalmol. Vis. Sci.. 2021; 62(8):2705.

ARVO Annual Meeting Abstract June 2020

Long term follow-up of Stargardt dystrophy

Jana Sajovic; Marko Hawlina; Maja Šuštar; Ana Fakin; Martina Jarc Vidmar

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):1049.

ARVO Annual Meeting Abstract June 2020

Phenotype and genotype spectrum of patients with a bilateral optic neuropathy in population of Slovenia

Sanja Petrovic Pajic; Martina Jarc Vidmar; Ana Fakin; Maja Šuštar; Jelka Brecelj; Luka Lapajne; Marija Volk; Aleš Maver; Borut Peterlin; Marko Hawlina

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):3121.

ARVO Annual Meeting Abstract June 2020

Outcomes of autologous neurosensory retinal free flap transplantation surgery evaluated by microperimetry and multifocal electroretinography

Xhevat Lumi; Maja Šuštar; Ana Fakin; Marko Hawlina; Sanja Petrovic Pajic

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):801.

Physiology and Pharmacology April 2020

Polymodal Sensory Transduction in Mouse Corneal Epithelial Cells

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Luka Lapajne; Monika Lakk; Oleg Yarishkin; Lara Gubeljak; Marko Hawlina; David Križaj
TAGS: calcium, chronic exertional compartment syndrome, cornea, corneal epithelial cells, epithelium, mechanotransduction, cellular, mice, trpv1 receptor, diagnostic imaging, edema
Invest. Ophthalmol. Vis. Sci.. 2020; 61(4):2. https://doi.org/10.1167/iovs.61.4.2

Includes: Supplemental Content

ARVO Annual Meeting Abstract July 2019

Corneal mechanotransduction drives TRPV4-dependent release of the transmitter ATP

Luka Lapajne; Monika Lakk; Lara Gubeljak; Oleg Yarishkin; Marko Hawlina; David Krizaj

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):916.

ARVO Annual Meeting Abstract July 2018

Association between donor-related, preservation and storage parameters on endothelial cell density after DMEK

Petra Schollmayer; Zala Luznik; Luka Lapajne; Marko Hawlina

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):2899.

ARVO Annual Meeting Abstract July 2018

Genotype and phenotype characteristics of Leber hereditary optic neuropathy (LHON) patients in Slovenia

Sanja Petrovic Pajic; Martina Jarc-Vidmar; Ana Fakin; Maja Sustar; Jelka Brecelj; Luka Lapajne; Damjan Glavac; Mojca Tajnik; Borut Peterlin; Marija Volk; Ales Maver; Marko Hawlina

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):2185.

ARVO Annual Meeting Abstract June 2017

Characterization of dendritic cell subtypes in native and cultured cadaveric human limbal tissue on amniotic membrane

Zala Luznik; Andreja Nataša Kopitar; Alojz Ihan; Marko Hawlina; Petra Schollmayer

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):982.

ARVO Annual Meeting Abstract June 2017

Genotype-phenotype correlations in patients with Usher syndrome type 2 harboring mutations in USH2A and ADGRV1

Marko Hawlina; Ana Fakin; Crystel Bonnet; Anne Kurtenbach; Saddek Mohand-Said; Ditta Zobor; Martina Jarc-Vidmar; Katarina Stingl; Francesco Testa; Francesca Simonelli; José Alain sahel; Isabelle S Audo; Eberhart Zrenner; Christine Petit

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):3227.

ARVO Annual Meeting Abstract September 2016

Effect of intact amniotic membrane orientation on the phenotypic potential of cultured limbal cells

Zala Luznik; Petra Schollmayer; Marina Bertolin; Elvira Maličev; Sofija Andjelić; Andreja Nataša Kopitar; Alojz Ihan; Stefano Ferrari; Marko Hawlina

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):4346.

ARVO Annual Meeting Abstract September 2016

Abnormal anterior lens epithelium in retinitis pigmentosa-related cataract – scanning and transmission electron microscopy study Hawlina M, MD, PhD 1 , Drašlar K, PhD 2 , Hvala A, PhD 3 , Andjelic S, PhD 1 1 Eye Hospital, University Medical Centre, Ljubljana, Slovenia 2 Department of Biology, Biotechnical Faculty, University of Ljubljana, Ljubljana, Slovenia 3 Department of Pathology, Medical Faculty, University of Ljubljana, Ljubljana, Slovenia

Marko Hawlina

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):2513.

ARVO Annual Meeting Abstract June 2013

Functional and molecular characterization of ex vivo cultured neuronal- and glial- like cells from internal limiting membrane

Xhevat Lumi; Sofija Andjelic; Erik Otter Johnsen; Morten Carstens Moe; Marko Hawlina; Goran Petrovski

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):6088.

ARVO Annual Meeting Abstract June 2013

A comprehensive screen of the USH2A gene in 185 patients with autosomal recessive retinal disease

Eva Lenassi; Zubin Saihan; Zheng Li; Marko Hawlina; Anthony Moore; Linda Luxon; Karen Steel; Maria Bitner-Glindzicz; Andrew Webster

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):677.

ARVO Annual Meeting Abstract June 2013

Multiple Rings or Arcs of Hyperautoflourescence in Different Retinitis Pigmentosa Phenotypes

Ana Fakin; Martina Jarc-Vidmar; Maja Šuštar; Jelka Brecelj; Branka Stirn Kranjc; Marko Hawlina

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):689.

ARVO Annual Meeting Abstract March 2012

Structural and Functional Correlations of Hyperautofluorescent Foveal Patch in Usher Syndrome Patients

Ana Fakin; Eva Lenassi; Martina Jarc-Vidmar; Damjan Glava; Crystel Bonnet; Christine Petit; Marko Hawlina

Invest. Ophthalmol. Vis. Sci.. 2012; 53(14):4597.

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

Relative preservation of central retinal layers in LHON in comparison to other optic neuropathies

TRPV4 involvement in inflammation and tissue damage in corneal epithelium

Electroretinography as a biomarker to monitor Stargardt disease

Characterisation of Stargardt disease pathogenesis associated with the frequent ABCA4 mutation c.5714+5G>A

Long term follow-up of Stargardt dystrophy

Phenotype and genotype spectrum of patients with a bilateral optic neuropathy in population of Slovenia

Outcomes of autologous neurosensory retinal free flap transplantation surgery evaluated by microperimetry and multifocal electroretinography

Polymodal Sensory Transduction in Mouse Corneal Epithelial Cells

Corneal mechanotransduction drives TRPV4-dependent release of the transmitter ATP

Association between donor-related, preservation and storage parameters on endothelial cell density after DMEK

Genotype and phenotype characteristics of Leber hereditary optic neuropathy (LHON) patients in Slovenia

Characterization of dendritic cell subtypes in native and cultured cadaveric human limbal tissue on amniotic membrane

Genotype-phenotype correlations in patients with Usher syndrome type 2 harboring mutations in USH2A and ADGRV1

Effect of intact amniotic membrane orientation on the phenotypic potential of cultured limbal cells

Functional and molecular characterization of ex vivo cultured neuronal- and glial- like cells from internal limiting membrane

A comprehensive screen of the USH2A gene in 185 patients with autosomal recessive retinal disease

Multiple Rings or Arcs of Hyperautoflourescence in Different Retinitis Pigmentosa Phenotypes

Structural and Functional Correlations of Hyperautofluorescent Foveal Patch in Usher Syndrome Patients

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