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Imaging & Retinal Dystrophies

10:00 - 11:30 | 07 September | Room: Speakers' Corner.

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10:00A retrospective cohort study exploring whether an association exists between spatial distribution of cystoid spaces in cystoid macular oedema secondary to Retinitis Pigmentosa and response to treatment with carbonic anhydrase inhibitors.
S. Strong UK
10:05A novel homozygous frameshift variant in the cellular retinaldehyde-binding protein 1 gene (RLBP1) causes retinitis punctata albescens
S. Costa Portugal
10:10A rare presentation of pigmented paravenous retinochoroidal atrophy
M. Prieto del Cura Spain
10:15Changes in the morphology of the macula in epiretinal fibrosis
O. Fayzrakhmanova Russia
10:20Choroidal thickness measurements using enhanced depth imaging OCT: the feasibility of automatic analysis in central serous retinopathy
S. Kasbia UK
10:30Evaluation of macular vessel density using SS-OCTA and morpho-functional correlation by microperimetry in patients with retinitis pigmentosa.
A. Vagge Italy
10:35Evaulation of macular microvascularity and choriocapillaris after pneumatic retinopexy
A. Karalezli Turkey
10:40Features of the choriocapillaris and choroidal vessels on 4 different optical coherence tomography angiography devices
K. Nam South Korea
10:45Impact of inherited retinal disease in Ireland and UK
O. Galvin Ireland
10:50Macular impairment in Fabry disease: a morpho-functional assessment by swept-source OCT angiography and focal electroretinography.
L. Barbano Italy
10:55Macular pattern dystrophy in maternally inherited diabetes and deafness (MIDD): 7 years progression, clues and implications of diagnosis
R. Burggraaf Sánchez de las Matas Spain
11:00Macular retinoschisis associated with glaucomatous optic neuropathy: Response to topical carbonic anhydrase inhibitor and trabeculectomy
M. Haruta Japan
11:05Multimodal imaging of late-onset retinal degeneration
N. Mandal UK
11:10OCT angiography of persistent hyaloid artery(pha): a case report
J. Kim South Korea
11:15Retinal and choroidal findings in autosomal recessive parkinson’s disease are similar to those in idiopathic parkinson’s disease
S. Kadayifcilar Turkey
11:20Rpe65 mutation in three siblings with lca resulting in variable phenotypic features
M. Magliyah Saudi Arabia
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