Optical coherence tomography angiography in the multimodal assessment of the retinal posterior pole in autosomal dominant optic atrophy

Optical Coherence Tomography Angiography in Glaucoma

(2020) Harsha L. Rao et al.   JOURNAL OF GLAUCOMA

ATPase Domain AFG3L2 Mutations Alter OPA1 Processing and Cause Optic Neuropathy

(2020) Leonardo Caporali et al.   ANNALS OF NEUROLOGY

Retinal and Choroidal Vasculature in Patients with Marfan Syndrome

(2020) Matteo Di Marino et al.   Translational Vision Science & Technology

Retinal capillary perfusion: Spatial and temporal heterogeneity

(2019) Dao-Yi Yu et al.   PROGRESS IN RETINAL AND EYE RESEARCH

Peripapillary and macular morpho-vascular changes in patients with genetic or clinical diagnosis of autosomal dominant optic atrophy: a case-control study

(2019) Amélia Martins et al.   GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY

OPA1: 516 unique variants and 831 patients registered in an updated centralized Variome database

(2019) Bastien Le Roux et al.   Orphanet Journal of Rare Diseases

Optical coherence tomography angiography

(2018) Richard F. Spaide et al.   PROGRESS IN RETINAL AND EYE RESEARCH

Quantitative Comparison of Retinal Vascular Features in Optical Coherence Tomography Angiography Images From Three Different Devices

(2018) Neha Anegondi et al.   Ophthalmic Surgery Lasers & Imaging Retina

The short variant of the mitochondrial dynamin OPA1 maintains mitochondrial energetics and cristae structure

(2017) Hakjoo Lee et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Optical coherence tomography angiography of the peripapillary retina and optic nerve head in dominant optic atrophy

(2017) Nicole Balducci et al.   MITOCHONDRION

Assessment of the retinal posterior pole in dominant optic atrophy by spectral-domain optical coherence tomography and microperimetry

(2017) Massimo Cesareo et al.   PLoS One

The reduction of temporal optic nerve head microcirculation in autosomal dominant optic atrophy

(2016) Maki Inoue et al.   ACTA OPHTHALMOLOGICA

Diagnostic ability of peripapillary vessel density measurements of optical coherence tomography angiography in primary open-angle and angle-closure glaucoma

(2016) Harsha L Rao et al.   BRITISH JOURNAL OF OPHTHALMOLOGY

Vessel Density Calculated from OCT Angiography in 3 Peripapillary Sectors in Normal, Ocular Hypertensive, and Glaucoma Eyes

(2016) Gábor Holló   EUROPEAN JOURNAL OF OPHTHALMOLOGY

Relationship between Optical Coherence Tomography Angiography Vessel Density and Severity of Visual Field Loss in Glaucoma

(2016) Adeleh Yarmohammadi et al.   OPHTHALMOLOGY

Correlation between optic disc perfusion and glaucomatous severity in patients with open-angle glaucoma: an optical coherence tomography angiography study

(2015) Xiaolei Wang et al.   GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY

Retinal vessel diameters decrease with macular ganglion cell layer thickness in autosomal dominant optic atrophy and in healthy subjects

(2014) Cecilia Rönnbäck et al.   ACTA OPHTHALMOLOGICA

Optical coherence tomography angiography of optic nerve head and parafovea in multiple sclerosis

(2014) Xiaogang Wang et al.   BRITISH JOURNAL OF OPHTHALMOLOGY

Dominant Optic Atrophy: Novel OPA1 Mutations and Revised Prevalence Estimates

(2013) Patrick Yu-Wai-Man et al.   OPHTHALMOLOGY

High-ResolutionEn FaceImages of Microcystic Macular Edema in Patients with Autosomal Dominant Optic Atrophy

(2013) Kiyoko Gocho et al.   Biomed Research International

SDOCT Thickness Measurements of Various Retinal Layers in Patients with Autosomal Dominant Optic Atrophy due toOPA1Mutations

(2013) Andrea M. Schild et al.   Biomed Research International

OPA1 Mutations Associated with Dominant Optic Atrophy Influence Optic Nerve Head Size

(2010) Piero Barboni et al.   OPHTHALMOLOGY

HISTOPATHOLOGY OF EYE, OPTIC NERVE AND BRAIN IN A CASE OF DOMINANT OPTIC ATROPHY

(2009) P. KJER et al.   ACTA OPHTHALMOLOGICA

The Molecular Mechanisms of OPA1-Mediated Optic Atrophy in Drosophila Model and Prospects for Antioxidant Treatment

(2008) Will Yarosh et al.   PLoS Genetics