31 – 40 of 66
- show: 10
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=" "
width=" "
height=" "
allowtransparency="true"
frameborder="0">
</iframe>
- 2018
-
Mark
Unilateral central retinal vein occlusion as a first manifestation of diabetes mellitus in a ten-year-old girl
(
- Contribution to journal › Article
-
Mark
Multimodal imaging in serologically confirmed Rubella retinopathy
(
- Contribution to journal › Article
-
Mark
Novel causative variants in patients with achromatopsia
(
- Contribution to journal › Article
-
Mark
Genetic Testing for Wolfram Syndrome Mutations in a Sample of 71 Patients with Hereditary Optic Neuropathy and Negative Genetic Test Results for OPA1/OPA3/LHON
(
- Contribution to journal › Article
-
Mark
Severe retinal degeneration at an early age in Usher syndrome type 1B associated with homozygous splice site mutations in MYO7A gene
(
- Contribution to journal › Article
-
Mark
Congenital stationary night blindness associated with morning glory disc malformation : a novel hemizygous mutation in CACNA1F
(
- Contribution to journal › Letter
- 2017
-
Mark
Variable Familial Exudative Vitreoretinopathy in a family harbouring variants in both FZD4 and TSPAN12
(
- Contribution to journal › Article
-
Mark
Multimodal imaging in CABP4-related retinopathy
(
- Contribution to journal › Article
-
Mark
Heterozygous mutation in OTX2 associated with early-onset retinal dystrophy with atypical maculopathy
(
- Contribution to journal › Article
-
Mark
Serous retinal detachment after panretinal photocoagulation for proliferative diabetic retinopathy : A case report
(
- Contribution to journal › Article