Diagnostic and Therapeutic Challenges
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Ophthalmology,General Medicine
Reference7 articles.
1. Macular pigment rings as the presenting finding of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes;Inoue;Retin Cases Brief Rep,2015
2. Diagnosis of maternally inherited diabetes and deafness (mitochondrial A3243G mutation) based on funduscopic appearance in an asymptomatic patient;Strauss;Br J Ophthalmol,2012
3. Characterisation of the macular dystrophy in patients with the A3243G mitochondrial DNA point mutation with fundus autofluorescence;Rath;Br J Ophthalmol,2008
4. Pattern dystrophy with high intrafamilial variability associated with Y141C mutation in the peripherin/RDS gene and successful treatment of subfoveal CNV related to multifocal pattern type with anti-VEGF (ranibizumab) intravitreal injections;Vaclavik;Retina,2012
5. Autosomal dominant pattern dystrophy: identification of a novel splice site mutation in the peripherin/RDS gene;Khoubian;Retina,2005
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