Ricardo A. Calderon-Murati

San Juan, Puerto Rico

Last Updated: 09/26/2026

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Found 12 publications

Stargardt Disease Presenting as Retinitis Pigmentosa: A Case of Monoallelic ABCA4-Associated Retinopathy.

Stargardt Disease Presenting as Retinitis Pigmentosa: A Case of Monoallelic ABCA4-Associated Retinopathy.

Journal: Cureus

Published: May 21, 2026

Clinical and Genetic Findings in an Autosomal Dominant Optic Atrophy-Compatible Phenotype Harboring an OPA1 Variant: A Case Report.

Clinical and Genetic Findings in an Autosomal Dominant Optic Atrophy-Compatible Phenotype Harboring an OPA1 Variant: A Case Report.

Journal: Cureus

Published: October 28, 2025

Ocular Findings in Siblings With Alagille Syndrome: A Report of Two Cases.

Ocular Findings in Siblings With Alagille Syndrome: A Report of Two Cases.

Journal: Cureus

Published: October 23, 2025

Sarcoidosis: A Mimicker of Ocular Cicatricial Pemphigoid.

Sarcoidosis: A Mimicker of Ocular Cicatricial Pemphigoid.

Journal: Cureus

Published: October 04, 2025

Repository Corticotropin Therapy for Refractory Noninfectious Inflammatory Ocular Diseases.

Repository Corticotropin Therapy for Refractory Noninfectious Inflammatory Ocular Diseases.

Journal: Journal of clinical medicine

Published: September 24, 2025

Idiopathic Sclerochoroidal Calcification With a Concurrent COL11A2 Variant: A Case Report.

Idiopathic Sclerochoroidal Calcification With a Concurrent COL11A2 Variant: A Case Report.

Journal: Cureus

Published: September 13, 2025

Basaloid Squamous Cell Carcinoma Involving the Orbit: A Case Report.

Basaloid Squamous Cell Carcinoma Involving the Orbit: A Case Report.

Journal: Cureus

Published: September 10, 2025

Bilateral Choroidal Metastases Mimicking Central Serous Chorioretinopathy: A Diagnostic Challenge.

Bilateral Choroidal Metastases Mimicking Central Serous Chorioretinopathy: A Diagnostic Challenge.

Journal: Cureus

Published: September 07, 2025

Sveinsson Chorioretinal Atrophy: A New Gene Variant.

Sveinsson Chorioretinal Atrophy: A New Gene Variant.

Journal: Cureus

Published: August 19, 2025

Analysis of the Body Mass Index of Latino Patients With Bardet-Biedl Syndrome.

Analysis of the Body Mass Index of Latino Patients With Bardet-Biedl Syndrome.

Journal: Cureus

Published: June 25, 2025

Retinitis Pigmentosa: From Genetic Insights to Innovative Therapeutic Approaches-A Literature Review.

Retinitis Pigmentosa: From Genetic Insights to Innovative Therapeutic Approaches-A Literature Review.

Journal: Medicina (Kaunas, Lithuania)

Published: May 25, 2025

A New Phenotypic Expression in a Patient With a Mutation in the CACNA1F Gene.

A New Phenotypic Expression in a Patient With a Mutation in the CACNA1F Gene.

Journal: Cureus

Published: April 19, 2025

Showing 1-12 of 12

Last Updated: 09/26/2026