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- 2023
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Mark
Cone dystrophy associated with autoimmune polyglandular syndrome type 1
(
- Contribution to journal › Article
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Mark
Leprel1-related Giant Retinal Tear Detachments Mimic the Phenotype of Ocular Stickler Syndrome
(
- Contribution to journal › Article
- 2022
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Mark
Unilateral Retinitis Pigmentosa Associated with Possible Ciliopathy and a Novel Mutation
(
- Contribution to journal › Article
- 2021
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Mark
Manifestation of panuveitis after intraocular surgery in a child with blau syndrome
(
- Contribution to journal › Article
-
Mark
Congenital stationary night blindness : an update and review of the disease spectrum in Saudi Arabia
(
- Contribution to journal › Scientific review
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Mark
Evolution of macular hole in enhanced S-cone syndrome
(
- Contribution to journal › Article
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Mark
Poretti-Boltshauser syndrome : a rare differential diagnosis to consider in pediatric high myopia with retinal degeneration
(
- Contribution to journal › Letter
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Mark
Clinical spectrum, genetic associations and management outcomes of Coats-like exudative retinal vasculopathy in autosomal recessive retinitis pigmentosa
(
- Contribution to journal › Article
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Mark
Association of the Recurrent Rare Variant c.415T>C p.Phe139Leu in CLN5 with a Recessively Inherited Macular Dystrophy
(
- Contribution to journal › Article
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Mark
Incidence and Natural History of Retinochoroidal Neovascularization in Enhanced S-Cone Syndrome
(
- Contribution to journal › Article
- 2020
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Mark
Late presentation of RPE65 retinopathy in three siblings
(
- Contribution to journal › Article
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Mark
Analysis of retinal function and structure in autosomal recessive retinal-renal ciliopathy
(
- Contribution to journal › Letter
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Mark
Long-term resolution of chronic macular edema after a single dose of intravitreal dexamethasone in familial retinal arterial macroaneurysm
(
- Contribution to journal › Letter
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Mark
Rhegmatogenous Retinal Detachment in Nonsyndromic High Myopia Associated with Recessive Mutations in LRPAP1
(
- Contribution to journal › Published meeting abstract
- 2019
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Mark
Multimodal retinal imaging in MFSD8-neuronal ceroid lipofuscinosis
(
- Contribution to journal › Letter