Search Results - JARC VIDMAR, M

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  1. 1
    Functional aspects of hyperautofluorescent ring in retinal dystrophies

    Functional aspects of hyperautofluorescent ring in retinal dystrophies by HAWLINA, M, LENASSI, E, FAKIN, A, JARC VIDMAR, M, BRECELJ, J

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  2. 2
    Assessment of fixation locus with microperimetry and OCT in patients with Stargardt disease

    Assessment of fixation locus with microperimetry and OCT in patients with Stargardt disease by LENASSI, E, JARC‐VIDMAR, M, HAWLINA, M

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  3. 3
    Microperimetry, PERG and mfERG in patients with Stargardt dystrophy

    Microperimetry, PERG and mfERG in patients with Stargardt dystrophy by JARC‐VIDMAR, M, POPOVIC, P, LENASSI, E, BRECELJ, J

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  4. 4
    Abnormal fundus autofluorescence in relation to retinal function in patients with retinitis pigmentosa

    Abnormal fundus autofluorescence in relation to retinal function in patients with retinitis pigmentosa by Popović, Petra, Jarc-Vidmar, Martina, Hawlina, Marko

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  5. 5
    Pattern ERG and psychophysical functions in Best's disease

    Pattern ERG and psychophysical functions in Best's disease by JARC-VIDMAR, M, POPOVIC, P, HAWLINA, M, BRECELJ, J

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  6. 6
    ABCA4 Variant c.5714+5G>A in Trans With Null Alleles Results in Primary RPE Damage

    ABCA4 Variant c.5714+5G>A in Trans With Null Alleles Results in Primary RPE Damage by Sajovic, Jana, Meglič, Andrej, Corradi, Zelia, Khan, Mubeen, Maver, Aleš, Vidmar, Martina Jarc, Hawlina, Marko, Cremers, Frans P. M., Fakin, Ana

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  7. 7
    Peripapillary retinal nerve fibre layer thinning in patients with X-linked retinoschisis

    Peripapillary retinal nerve fibre layer thinning in patients with X-linked retinoschisis by Kiraly, Peter, Gavrić, Ana Uršula, Reichel, Felix F, Birtel, Johannes, Mautone, Luca, Atiskova, Yevgeniya, Herrmann, Philipp, Jarc-Vidmar, Martina, Hawlina, Marko, Downes, Susan M, Fischer, M Dominik

    Published in BMJ open ophthalmology
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  8. 8
    An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients

    An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients by Bonnet, Crystel, Riahi, Zied, Chantot-Bastaraud, Sandra, Smagghe, Luce, Letexier, Mélanie, Marcaillou, Charles, Lefèvre, Gaëlle M, Hardelin, Jean-Pierre, El-Amraoui, Aziz, Singh-Estivalet, Amrit, Mohand-Saïd, Saddek, Kohl, Susanne, Kurtenbach, Anne, Sliesoraityte, Ieva, Zobor, Ditta, Gherbi, Souad, Testa, Francesco, Simonelli, Francesca, Banfi, Sandro, Fakin, Ana, Glavač, Damjan, Jarc-Vidmar, Martina, Zupan, Andrej, Battelino, Saba, Martorell Sampol, Loreto, Claveria, Maria Antonia, Catala Mora, Jaume, Dad, Shzeena, Møller, Lisbeth B, Rodriguez Jorge, Jesus, Hawlina, Marko, Auricchio, Alberto, Sahel, José-Alain, Marlin, Sandrine, Zrenner, Eberhart, Audo, Isabelle, Petit, Christine

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  9. 9
    Morphological and functional parameters in X-linked retinoschisis patients-A multicentre retrospective cohort study

    Morphological and functional parameters in X-linked retinoschisis patients-A multicentre retrospective cohort study by Kiraly, Peter, Seitz, Immanuel P, Abdalla Elsayed, Maram E A, Downes, Susan M, Patel, Chetan K, Charbel Issa, Peter, Birtel, Johannes, Mautone, Luca, Dulz, Simon, Atiskova, Yevgeniya, Herrmann, Philipp, Vrabič, Nika, Jarc-Vidmar, Martina, Hawlina, Marko, Fischer, M Dominik

    Published in Frontiers in medicine
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