| 1 |
Macular involvement in congenital aniridia |
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| P. Casas-Llera,D. Ruiz-Casas,J.L. Alió |
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| Archivos de la Sociedad Española de Oftalmología (English Edition). 2021; |
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| 2 |
Alteraciones maculares en aniridia congénita |
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| P. Casas-Llera,D. Ruiz-Casas,J.L. Alió |
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| Archivos de la Sociedad Española de Oftalmología. 2021; |
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| 3 |
Retinal Architecture in Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay
(ARSACS)
: Insights into Disease Pathogenesis and Biomarkers |
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| Flávio Moura Rezende Filho,Fion Bremner,José Luiz Pedroso,João Brainer Clares Andrade,Bruna Ferraço Marianelli,Charles Marques Lourenço,Wilson Marques-Júnior,Marcondes C. França,Fernando Kok,Juliana M.F. Sallum,Michael H. Parkinson,Orlando G. Barsottini,Paola Giunti |
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| Movement Disorders. 2021; |
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| 4 |
Foveal avascular zone in oculocutaneous albinism |
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| Hana A Mansour,Sami Uwaydat,Muhamad H Yunis,Ahmad M Mansour |
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| BMJ Case Reports. 2021; 14(5): e240208 |
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| 5 |
Novel Biallelic Variants and Phenotypic Features in Patients with SLC38A8-Related Foveal Hypoplasia |
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| Elena R. Schiff,Vijay K. Tailor,Hwei Wuen Chan,Maria Theodorou,Andrew R. Webster,Mariya Moosajee |
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| International Journal of Molecular Sciences. 2021; 22(3): 1130 |
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| 6 |
Genetic causes of nystagmus, foveal hypoplasia and subnormal visual acuity- other than albinism |
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| Miriam Ehrenberg,Laura Bagdonite-Bejarano,Anne B. Fulton,Naama Orenstein,Claudia Yahalom |
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| Ophthalmic Genetics. 2021; : 1 |
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Bilateral atypical lamellar holes in a patient with oculocutaneous albinism |
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| Michelle M. Falcone,Nimesh A. Patel,Nicolas A. Yannuzzi,Dhariana Acon,Catherin I. Negron,Craig McKeown,Audina M. Berrocal |
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| Ophthalmic Genetics. 2020; : 1 |
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| 8 |
Septo-optic dysplasia with fovea plana: A case report |
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| Ali Keles,Cagri Ilhan,Mehmet Yasin Teke,Kemal Tekin |
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| European Journal of Ophthalmology. 2020; 30(5): NP36 |
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| 9 |
Multimodal imaging of fovea plana in oculocutaneous albinism |
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| SimarR Singh,Sahil Jain,Savleen Kaur,Mohit Dogra |
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| Indian Journal of Ophthalmology. 2019; 67(10): 1733 |
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