When a large refractive error is found in children, should we immediately order electroretinography?
Clinical and Genetic Features of Korean Patients with Achromatopsia
Preventable risk factors for type 2 diabetes can be detected
CDHR1-Related Cone–Rod Dystrophy
pward saccadic intrusions as the presenting feature for incomplete congenital stationary night blindness.
A Japanese boy with Bardet-Biedl syndrome caused by a novel homozygous variant
Whole-Exome Sequencing and Copy Number Analysis in a Patient with Warburg Micro Syndrome
Evaluation of Electroretinograms Using RETeval in Preterm Infants without Retinopathy of Prematurity.
Are we overlooking the neurodegeneration in the early stage of Type 1 Diabetes Mellitus without Visual Impairment or Diabetic Retinopathy
Phenotypic Variation of Autosomal Recessive Leber Hereditary Optic Neuropathy (arLHON) in One Family
Transient Increase of Flicker Electroretinography Amplitudes after Cataract Surgery
The Development of Electroretinographic Oscillatory Potentials in Healthy Young Children.
