Spectral-domain optical coherence tomography: a comparison of modern high-resolution retinal imaging systems
PURPOSE: To provide a review of commercially available spectral-domain optical
coherence tomography (SD OCT) systems in clinical ophthalmology. DESIGN: Perspective …
coherence tomography (SD OCT) systems in clinical ophthalmology. DESIGN: Perspective …
Macular dystrophies mimicking age-related macular degeneration
NTM Saksens, M Fleckenstein… - Progress in retinal and …, 2014 - Elsevier
Age-related macular degeneration (AMD) is the leading cause of irreversible blindness in
the elderly population in the Western world. AMD is a clinically heterogeneous disease …
the elderly population in the Western world. AMD is a clinically heterogeneous disease …
Fundus autofluorescence imaging in hereditary retinal diseases
F Pichi, EB Abboud, NG Ghazi… - Acta ophthalmologica, 2018 - Wiley Online Library
Fundus autofluorescence (FAF) is a non‐invasive retinal imaging modality used in clinical
practice to non‐invasively map changes at the level of the retinal pigment epithelium …
practice to non‐invasively map changes at the level of the retinal pigment epithelium …
Multimodal imaging and functional testing in a North Carolina macular disease family: toxoplasmosis, fovea plana, and torpedo maculopathy are phenocopies
KW Small, EM Tran, L Small, RC Rao, F Shaya - Ophthalmology Retina, 2019 - Elsevier
Purpose To describe multimodal imaging and corresponding functional studies in a newly
found family with North Carolina macular dystrophy (NCMD). To our knowledge, this is an …
found family with North Carolina macular dystrophy (NCMD). To our knowledge, this is an …
[HTML][HTML] Clinical and genetic characterization of a Danish family with North Carolina macular dystrophy
T Rosenberg, B Roos, T Johnsen, N Bech… - Molecular …, 2010 - ncbi.nlm.nih.gov
Purpose To describe the phenotype of a family with an autosomal dominant macular
dystrophy and identify the chromosomal location of the gene that causes this phenotype …
dystrophy and identify the chromosomal location of the gene that causes this phenotype …
Multimodal imaging in hereditary retinal diseases
Introduction. In this retrospective study we evaluated the multimodal visualization of retinal
genetic diseases to better understand their natural course. Material and Methods. We …
genetic diseases to better understand their natural course. Material and Methods. We …
A novel tandem duplication of PRDM13 in a Chinese family with North Carolina macular dystrophy
S Wu, Z Yuan, Z Sun, T Zhu, X Wei, X Zou… - Graefe's Archive for …, 2022 - Springer
Abstract Purposes North Carolina macular dystrophy (NCMD) is a rare autosomal dominant
inherited disorder characterized by macular impairment with a variety of phenotypic …
inherited disorder characterized by macular impairment with a variety of phenotypic …
Outcomes of treatment of pediatric choroidal neovascularization with intravitreal antiangiogenic agents: the results of the KKESH International Collaborative Retina …
Purpose: To evaluate safety and clinical results of intravitreal antiangiogenic agents for
choroidal neovascularization in pediatric patients. Methods: Retrospective, multicenter …
choroidal neovascularization in pediatric patients. Methods: Retrospective, multicenter …
Choroidal cavitary disorders
S Nassar, AK Tarbett, DJ Browning - Clinical Ophthalmology, 2020 - Taylor & Francis
The structure and functions of the choroid have been long acknowledged but the
pathophysiology behind various anomalies has been difficult to understand until the advent …
pathophysiology behind various anomalies has been difficult to understand until the advent …
Thirty-Year follow-up of an African American family with macular dystrophy of the retina, locus 1 (North Carolina macular dystrophy)
PURPOSE:: To describe clinical characteristics, including visual acuity (VA), genetic
analysis, and management of complications, over a 30-year period in an African American …
analysis, and management of complications, over a 30-year period in an African American …