23 results on '"Santos-Silva, Renato"'
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2. What to expect from primary inferior oblique overaction after esotropia surgery: Primary inferior oblique overaction in esotropia
3. The Red Reflex Test and Leukocoria in Childhood.
4. Child with a mild phenotype of Incontinentia Pigmenti and inner retinal dysfunction
5. Unraveling Hermansky–Pudlak syndrome type 7: a case report and comprehensive literature review on the identification of DTNBP1 variants.
6. Cohen Syndrome: Novel VPS13B Genetic Variants in a Male Portuguese Patient with Pigmentary Retinopathy
7. What to Expect from Primary Inferior Oblique Overaction After Esotropia Surgery
8. Tratamento Cirúrgico da Parésia do Quarto Par Craniano: Uma Série de Casos
9. Cirurgia de Estrabismo para Corrigir Posição Anómala Cabeça: 7 Anos de Experiência num Hospital Terciário
10. Cone dystrophy with supernormal rod responses: A rare KCNV2 gene variant
11. Idiopathic Acute Exudative Polymorphous Vitelliform Maculopathy: Insight into Imaging Features and Outcomes
12. Cone dystrophy with supernormal rod responses: A rare KCNV2 gene variant.
13. Longitudinal Retinal Changes Induced by Hydroxychloroquine in Eyes without Retinal Toxicity
14. A novel MFRP gene variant in a family with posterior microphthalmos, retinitis pigmentosa, foveoschisis, and foveal hypoplasia
15. A novel homozygous frameshift variant in the cellular retinaldehyde-binding protein 1 (RLBP1) gene causes retinitis punctata albescens
16. A novel homozygous frameshift variant in the cellular retinaldehyde-binding protein 1 (RLBP1) gene causes retinitis punctata albescens.
17. Adequacy of the Fogging Test in the Detection of Clinically Significant Hyperopia in School-Aged Children
18. Longitudinal Retinal Changes Induced by Hydroxychloroquine in Eyes without Retinal Toxicity.
19. Early Longitudinal Spectral Domain Optical Coherence Tomography Findings in Subacute Sclerosing Panencephalitis
20. Factors Predictive of Success in Probing for Congenital Nasolacrimal Duct Obstruction
21. Urgência de Oftalmologia Pediátrica no Norte de Portugal
22. Presumed Bilateral Cilioretinal Artery Occlusion Related to Relapsing White Dot Syndrome
23. Cohen Syndrome: Novel VPS13B Genetic Variants in a Male Portuguese Patient with Pigmentary Retinopathy.
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