Past, present and future role of retinal imaging in neurodegenerative disease

AH Kashani, S Asanad, JW Chan, MB Singer… - Progress in retinal and …, 2021 - Elsevier
Retinal imaging technology is rapidly advancing and can provide ever-increasing amounts
of information about the structure, function and molecular composition of retinal tissue in …

Ultra-widefield fundus imaging: a review of clinical applications and future trends

A Nagiel, RA Lalane, SVR Sadda, SD Schwartz - Retina, 2016 - journals.lww.com
Purpose: To review the basic principles of ultra-widefield fundus imaging and discuss its
clinical utility for a variety of retinal and choroidal disorders. Methods: A systematic review of …

Ultra-widefield retinal imaging: an update on recent advances

SN Patel, A Shi, TD Wibbelsman… - Therapeutic advances …, 2020 - journals.sagepub.com
The development of ultra-widefield retinal imaging has accelerated our understanding of
common retinal diseases. As we continue to validate the diagnostic and prognostic …

Ultra-wide field retinal imaging: A wider clinical perspective

V Kumar, A Surve, D Kumawat, B Takkar… - Indian Journal of …, 2021 - journals.lww.com
The peripheral retina is affected in a variety of retinal disorders. Traditional fundus cameras
capture only a part of the fundus even when montaging techniques are used. Ultra-wide field …

[HTML][HTML] Familial exudative vitreoretinopathy: pathophysiology, diagnosis, and management

Z Tauqeer, Y Yonekawa - Asia-Pacific journal of ophthalmology, 2018 - Elsevier
Familial exudative vitreoretinopathy (FEVR) is a heritable vitreoretinopathy characterized by
anomalous retinal vascular development. The principal feature of the disease is an …

TSPAN12 is a Norrin co-receptor that amplifies Frizzled4 ligand selectivity and signaling

MB Lai, C Zhang, J Shi, V Johnson, L Khandan… - Cell reports, 2017 - cell.com
Accessory proteins in Frizzled (FZD) receptor complexes are thought to determine ligand
selectivity and signaling amplitude. Genetic evidence indicates that specific combinations of …

Haploinsufficiency of RCBTB1 is associated with Coats disease and familial exudative vitreoretinopathy

JH Wu, JH Liu, YC Ko, CT Wang… - Human molecular …, 2016 - academic.oup.com
Familial exudative vitreoretinopathy (FEVR) belongs to a group of genetically and clinically
heterogeneous disorders in retinal vascular development. To date, in approximately 50% of …

Spectrum of variants in 389 Chinese probands with familial exudative vitreoretinopathy

JK Li, Y Li, X Zhang, CL Chen, YQ Rao… - … & Visual Science, 2018 - iovs.arvojournals.org
Purpose: To identify potentially pathogenic variants (PPVs) in Chinese familial exudative
vitreoretinopathy (FEVR) patients in FZD4, LRP5, NDP, TSPAN12, ZNF408, and KIF11 …

Familial exudative vitreoretinopathy: spectral-domain optical coherence tomography of the vitreoretinal interface, retina, and choroid

Y Yonekawa, BJ Thomas, KA Drenser, MT Trese… - Ophthalmology, 2015 - Elsevier
Purpose The in vivo microstructural features of familial exudative vitreoretinopathy (FEVR)
have not been well described. We present new anatomic features of FEVR with functional …

Retinopathy of prematurity versus familial exudative vitreoretinopathy: report on clinical and angiographic findings

VJ John, JI McClintic, DJ Hess… - … Surgery, Lasers and …, 2016 - journals.healio.com
BACKGROUND AND OBJECTIVE: Retinopathy of prematurity (ROP) and familial exudative
vitreoretinopathy (FEVR) are classified as distinct diseases; however, emerging genetic …