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ORSANMICHELE
December, 07th | 17:30 - 18:45
FREE PAPERS - INHERITED RETINAL DYSTROPHIES
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Chairs: HUANG SUBER, LEROY BART, SIMONELLI FRANCESCA
December, 07th | 17:30 - 17:33
Optical coherence tomography biomarkers in inherited macular disorders- series of cases
SONJA CEKIC
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Optical coherence tomography biomarkers in inherited macular disorders- series of cases
SONJA CEKIC
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December, 07th | 17:33 - 17:36
Cellular analysis of retinal pigment epithelium and photoreceptors by transscleral optical phase imaging in impg2-related inherited retinal dystrophy
LOMBARDO MARCO
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Cellular analysis of retinal pigment epithelium and photoreceptors by transscleral optical phase imaging in impg2-related inherited retinal dystrophy
LOMBARDO MARCO
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December, 07th | 17:36 - 17:39
Membrane-type frizzled related protein: a comprehensive analysis of genetic characteristics, phenotypic manifestations and impact on retinal microvasculature
AYATA SELIM
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Membrane-type frizzled related protein: a comprehensive analysis of genetic characteristics, phenotypic manifestations and impact on retinal microvasculature
AYATA SELIM
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December, 07th | 17:39 - 17:42
Drusen volume as clinical outcome measure in subjects with malattia leventinese
EHRENZELLER CLARA
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Drusen volume as clinical outcome measure in subjects with malattia leventinese
EHRENZELLER CLARA
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December, 07th | 17:42 - 17:45
Swept-source optical coherence tomography changes and visual acuity among Palestinian retinitis pigmentosa patients: a cross-sectional study
ALTALBISHI ALAA
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Swept-source optical coherence tomography changes and visual acuity among Palestinian retinitis pigmentosa patients: a cross-sectional study
ALTALBISHI ALAA
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December, 07th | 17:45 - 17:48
OCT Analysis and macular pigment optical density assessment in patients affected by retinitis pigmentosa
BELLONI BARONI LUCA
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OCT Analysis and macular pigment optical density assessment in patients affected by retinitis pigmentosa
BELLONI BARONI LUCA
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December, 07th | 17:48 - 17:51
Retinal oxygen metabolic function in choroideremia and retinitis pigmentosa
PRÉTOT DOMINIQUE
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Retinal oxygen metabolic function in choroideremia and retinitis pigmentosa
PRÉTOT DOMINIQUE
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December, 07th | 17:51 - 17:54
Protein mediators in aqueous humor samples of retinitis pigmentosa patients: identification of potential biomarkers.
MARTELLA SALVATORE
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Protein mediators in aqueous humor samples of retinitis pigmentosa patients: identification of potential biomarkers.
MARTELLA SALVATORE
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December, 07th | 17:54 - 17:57
Long-term outcomes of anti-VEGF therapy for macular neovascularization in PRPH2-associated retinopathy
TOSCANI REBECCA
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Long-term outcomes of anti-VEGF therapy for macular neovascularization in PRPH2-associated retinopathy
TOSCANI REBECCA
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December, 07th | 17:57 - 18:00
Ophthalmic manifestations and natural history of PRPH2 deletion-associated pattern dystrophy: a case series
CREMONESI PIERLUCA
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Ophthalmic manifestations and natural history of PRPH2 deletion-associated pattern dystrophy: a case series
CREMONESI PIERLUCA
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December, 07th | 18:00 - 18:03
Phenotypic and genotypic landscape of rp1l1-associated retinopathy
ANTROPOLI ALESSIO
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Phenotypic and genotypic landscape of rp1l1-associated retinopathy
ANTROPOLI ALESSIO
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December, 07th | 18:03 - 18:06
WDR19-associated retinopathy presenting with adult-onset stargardt-like phenotype
NUNZIATA ANNAMARIA
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WDR19-associated retinopathy presenting with adult-onset stargardt-like phenotype
NUNZIATA ANNAMARIA
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December, 07th | 18:06 - 18:09
Extensive macular atrophy with pseudodrusen-like appearance (EMAP): progression kinetics and late-stage findings
ANTROPOLI ALESSIO
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Extensive macular atrophy with pseudodrusen-like appearance (EMAP): progression kinetics and late-stage findings
ANTROPOLI ALESSIO
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December, 07th | 18:09 - 18:12
Full-field electroretinogram in extensive macular atrophy with pseudodrusen-like appearance (EMAP)
BIANCO LORENZO
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Full-field electroretinogram in extensive macular atrophy with pseudodrusen-like appearance (EMAP)
BIANCO LORENZO
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December, 07th | 18:12 - 18:15
Phenotypic variability and evolution of mfsd8-related inherited retinal disease
PANAGIOTOU EVANGELIA
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Phenotypic variability and evolution of mfsd8-related inherited retinal disease
PANAGIOTOU EVANGELIA
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December, 07th | 18:15 - 18:18
Shwachman-diamond syndrome and concurrent rod-cone dystrophy: report of two cases and literature review
BALDESI JACOPO
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Shwachman-diamond syndrome and concurrent rod-cone dystrophy: report of two cases and literature review
BALDESI JACOPO
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December, 07th | 18:18 - 18:21
Methylentetrahydrofolate reductase c677t mutation and the retinal and optic nerve head structure and function: an OCT-A study
KIRKOVA RADINA
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Methylentetrahydrofolate reductase c677t mutation and the retinal and optic nerve head structure and function: an OCT-A study
KIRKOVA RADINA
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December, 07th | 18:21 - 18:24
Tissue plasminogen activator-assisted vitrectomy and gas tamponade for submacular hemorrhage due to choroidal neovascularization secondary to angioid streaks: a case report
FINOCCHIO LUCIA
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Tissue plasminogen activator-assisted vitrectomy and gas tamponade for submacular hemorrhage due to choroidal neovascularization secondary to angioid streaks: a case report
FINOCCHIO LUCIA
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December, 07th | 18:24 - 18:27
Dexamethasone intravitreal implant for Muller cell sheen dystrophy treatment. a clinical case.
VOSKRESENSKAYA ANNA
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Dexamethasone intravitreal implant for Muller cell sheen dystrophy treatment. a clinical case.
VOSKRESENSKAYA ANNA
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