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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. doi: https://doi.org/

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. doi: https://doi.org/

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. doi: https://doi.org/

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. doi: https://doi.org/

ARVO Annual Meeting Abstract April 2011

Prevalence and Autofluorescence Patterns in Usher Syndrome in Slovenian Population

Ana Fakin; Eva Lenassi; Martina Jarc-Vidmar; Marko Hawlina

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):4980. doi: https://doi.org/

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