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Cureus
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May 20, 2025
A New Phenotypic Expression in a Patient With a Mutation in the CACNA1F Gene
Ricardo A Murati Calderon, Natalio Izquierdo
Cureus
|
December 1, 2025
Clinical and Genetic Findings in an Autosomal Dominant Optic Atrophy-Compatible Phenotype Harboring an OPA1 Variant: A Case Report
Ricardo A Murati Calderon, Gabriella Landestoy, Natalio Izquierdo
Cureus
|
June 22, 2026
Stargardt Disease Presenting as Retinitis Pigmentosa: A Case of Monoallelic ABCA4-Associated Retinopathy
Kevin Santiago-Narváez, Ricardo A Murati Calderon, Natalio Izquierdo
Cureus
|
October 16, 2025
Idiopathic Sclerochoroidal Calcification With a Concurrent COL11A2 Variant: A Case Report
Ricardo A Murati Calderon, Victor M Villegas, Armando Oliver
Cureus
|
November 26, 2025
Ocular Findings in Siblings With Alagille Syndrome: A Report of Two Cases
Ricardo A Murati Calderon, Julian A Menendez Sepulveda, Natalio Izquierdo
Journal of Clinical Medicine
|
November 13, 2025
Repository Corticotropin Therapy for Refractory Noninfectious Inflammatory Ocular Diseases
Christian Nieves-Ríos, Ricardo A Murati Calderon, Armando L Oliver
Cureus
|
July 28, 2025
Analysis of the Body Mass Index of Latino Patients With Bardet-Biedl Syndrome
Ricardo A Murati Calderon, Sebastián J Vázquez-Folch, Natalio Izquierdo
Cureus
|
September 23, 2025
Sveinsson Chorioretinal Atrophy: A New Gene Variant
Ricardo A Murati Calderon, Sebastián J Vázquez-Folch, Natalio Izquierdo
Cureus
|
November 6, 2025
Sarcoidosis: A Mimicker of Ocular Cicatricial Pemphigoid
Ricardo A Murati Calderon, José J López-Fontanet, Estefania Ramirez Marquez, et al.
Cureus
|
October 10, 2025
Bilateral Choroidal Metastases Mimicking Central Serous Chorioretinopathy: A Diagnostic Challenge
Ricardo A Murati Calderon, Christian Nieves-Ríos, Luis F Nieves Garrastegui, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 11) with videos related to
Sort By:
Page
of 2
Cureus
|
May 20, 2025
A New Phenotypic Expression in a Patient With a Mutation in the CACNA1F Gene
Ricardo A Murati Calderon, Natalio Izquierdo
Cureus
|
December 1, 2025
Clinical and Genetic Findings in an Autosomal Dominant Optic Atrophy-Compatible Phenotype Harboring an OPA1 Variant: A Case Report
Ricardo A Murati Calderon, Gabriella Landestoy, Natalio Izquierdo
Cureus
|
June 22, 2026
Stargardt Disease Presenting as Retinitis Pigmentosa: A Case of Monoallelic ABCA4-Associated Retinopathy
Kevin Santiago-Narváez, Ricardo A Murati Calderon, Natalio Izquierdo
Cureus
|
October 16, 2025
Idiopathic Sclerochoroidal Calcification With a Concurrent COL11A2 Variant: A Case Report
Ricardo A Murati Calderon, Victor M Villegas, Armando Oliver
Cureus
|
November 26, 2025
Ocular Findings in Siblings With Alagille Syndrome: A Report of Two Cases
Ricardo A Murati Calderon, Julian A Menendez Sepulveda, Natalio Izquierdo
Journal of Clinical Medicine
|
November 13, 2025
Repository Corticotropin Therapy for Refractory Noninfectious Inflammatory Ocular Diseases
Christian Nieves-Ríos, Ricardo A Murati Calderon, Armando L Oliver
Cureus
|
July 28, 2025
Analysis of the Body Mass Index of Latino Patients With Bardet-Biedl Syndrome
Ricardo A Murati Calderon, Sebastián J Vázquez-Folch, Natalio Izquierdo
Cureus
|
September 23, 2025
Sveinsson Chorioretinal Atrophy: A New Gene Variant
Ricardo A Murati Calderon, Sebastián J Vázquez-Folch, Natalio Izquierdo
Cureus
|
November 6, 2025
Sarcoidosis: A Mimicker of Ocular Cicatricial Pemphigoid
Ricardo A Murati Calderon, José J López-Fontanet, Estefania Ramirez Marquez, et al.
Cureus
|
October 10, 2025
Bilateral Choroidal Metastases Mimicking Central Serous Chorioretinopathy: A Diagnostic Challenge
Ricardo A Murati Calderon, Christian Nieves-Ríos, Luis F Nieves Garrastegui, et al.
Page
of 2