Andrea Sodi

Florence, Italy

Last Updated: 09/26/2026

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Found 110 publications

Choroidal measurements in patients affected by PXE-related retinopathy.

Choroidal measurements in patients affected by PXE-related retinopathy.

Journal: Frontiers in ophthalmology

Published: June 15, 2025

CHRONIC CENTRAL SEROUS CHORIORETINOPATHY WITHIN THREE FIRST-DEGREE RELATIVES: A CASE REPORT FROM AN ITALIAN FAMILY.

CHRONIC CENTRAL SEROUS CHORIORETINOPATHY WITHIN THREE FIRST-DEGREE RELATIVES: A CASE REPORT FROM AN ITALIAN FAMILY.

Journal: Retinal cases & brief reports

Published: March 18, 2025

Genotype-phenotype relationship in RDH12 retinopathy: a perspective from a pediatric age group.

Genotype-phenotype relationship in RDH12 retinopathy: a perspective from a pediatric age group.

Journal: Ophthalmic genetics

Published: March 05, 2025

Retinal Dystrophies Associated with Mutations in the RP1 Gene: Genotype-Phenotype Correlations.

Retinal Dystrophies Associated with Mutations in the RP1 Gene: Genotype-Phenotype Correlations.

Journal: Current issues in molecular biology

Published: December 03, 2024

CD3+CD4-CD8- Double-Negative Lymphocytes Are Increased in the Aqueous Humor of Patients with Retinitis Pigmentosa: Their Possible Role in Mediating Inflammation.

CD3+CD4-CD8- Double-Negative Lymphocytes Are Increased in the Aqueous Humor of Patients with Retinitis Pigmentosa: Their Possible Role in Mediating Inflammation.

Journal: International journal of molecular sciences

Published: October 20, 2024

Spontaneous Ectopia Lentis in Retinitis Pigmentosa: A Case Report and Review of the Literature.

Spontaneous Ectopia Lentis in Retinitis Pigmentosa: A Case Report and Review of the Literature.

Journal: Medicina (Kaunas, Lithuania)

Published: June 14, 2024

Myopic Macular Hole and Detachment after Gene Therapy in Atypical RPE65 Retinal Dystrophy: A Case Report.

Myopic Macular Hole and Detachment after Gene Therapy in Atypical RPE65 Retinal Dystrophy: A Case Report.

Journal: Genes

Published: May 12, 2024

Atypic Retinitis Pigmentosa Clinical Features Associated with a Peculiar CRX Gene Mutation in Italian Patients.

Atypic Retinitis Pigmentosa Clinical Features Associated with a Peculiar CRX Gene Mutation in Italian Patients.

Journal: Medicina (Kaunas, Lithuania)

Published: April 24, 2024

Inner retinal hyper-reflective foci number correlates with flood-illumination adaptive optics ophthalmoscopy grading and systemic organ involvement in patients with Fabry disease.

Inner retinal hyper-reflective foci number correlates with flood-illumination adaptive optics ophthalmoscopy grading and systemic organ involvement in patients with Fabry disease.

Journal: Eye (London, England)

Published: April 14, 2024

Optical coherence tomography (OCT) and OCT-angiography in syndromic versus non-syndromic USH2A-associated retinopathy.

Optical coherence tomography (OCT) and OCT-angiography in syndromic versus non-syndromic USH2A-associated retinopathy.

Journal: European journal of ophthalmology

Published: April 11, 2024

Multimodal phenotyping of foveal hypoplasia in albinism and albino-like conditions: a pediatric case series with adaptive optics insights.

Multimodal phenotyping of foveal hypoplasia in albinism and albino-like conditions: a pediatric case series with adaptive optics insights.

Journal: Scientific reports

Published: January 02, 2024

Voretigene neparvovec for inherited retinal dystrophy due to RPE65 mutations: a scoping review of eligibility and treatment challenges from clinical trials to real practice.

Voretigene neparvovec for inherited retinal dystrophy due to RPE65 mutations: a scoping review of eligibility and treatment challenges from clinical trials to real practice.

Journal: Eye (London, England)

Published: September 05, 2023

Showing 1-12 of 110

Last Updated: 09/26/2026