Renato Silva-Santos
Porto, Portugal
Last Updated: 09/26/2026
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Found 15 publications
Surgical management of hypotropia and exotropia in high myopia: a case report.
Journal: Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus
Published: November 28, 2024
Idiopathic Acute Exudative Polymorphous Vitelliform Maculopathy: A Case Report.
Journal: International medical case reports journal
Published: November 20, 2024
A Newborn Presenting with Alternating Bradycardia and Tachycardia.
Journal: NeoReviews
Published: September 14, 2024
Unraveling Hermansky-Pudlak syndrome type 7: a case report and comprehensive literature review on the identification of DTNBP1 variants.
Journal: Ophthalmic genetics
Published: December 15, 2023
Cohen Syndrome: Novel VPS13B Genetic Variants in a Male Portuguese Patient with Pigmentary Retinopathy.
Journal: Case reports in ophthalmology
Published: July 12, 2023
Revisiting Posterior Fixation Sutures Surgery: Unveiling Novel Approaches for Primary Management of Diverse Esotropia Cases.
Journal: Ophthalmology and therapy
Published: June 17, 2023
What to expect from primary inferior oblique overaction after esotropia surgery : Primary inferior oblique overaction in esotropia.
Journal: BMC ophthalmology
Published: April 10, 2023
Cone dystrophy with supernormal rod responses: A rare KCNV2 gene variant.
Journal: European journal of ophthalmology
Published: March 12, 2021
A novel MFRP gene variant in a family with posterior microphthalmos, retinitis pigmentosa, foveoschisis, and foveal hypoplasia.
Journal: Ophthalmic genetics
Published: July 25, 2020
Longitudinal Retinal Changes Induced by Hydroxychloroquine in Eyes without Retinal Toxicity.
Journal: Ophthalmic research
Published: June 30, 2020
Child with a mild phenotype of Incontinentia Pigmenti and inner retinal dysfunction.
Journal: Documenta ophthalmologica. Advances in ophthalmology
Published: May 16, 2020
A novel homozygous frameshift variant in the cellular retinaldehyde-binding protein 1 (RLBP1) gene causes retinitis punctata albescens.
Journal: European journal of ophthalmology
Published: April 30, 2020
Last Updated: 09/26/2026