EDITORIAL
Published on 14 Aug 2024
Editorial: Novel frontiers of retinal neurodegenerative diseases
doi 10.3389/fmed.2024.1470998
- 800 views
- Frontiers in Medicine
- Ophthalmology
- Research Topics
- Novel Frontiers of Retinal Neurodegenerative Diseases
Novel Frontiers of Retinal Neurodegenerative Diseases
4,519
Total downloads
18k
Total views and downloads
Articles
REVIEW
Published on 01 Jul 2024
Modeling inherited retinal diseases using human induced pluripotent stem cell derived photoreceptor cells and retinal pigment epithelial cells
doi 10.3389/fmed.2024.1328474
- 1,859 views
- 1 citation
ORIGINAL RESEARCH
Published on 05 Jun 2024
Elucidating the multifaceted roles of GPR146 in non-specific orbital inflammation: a concerted analytical approach through the prisms of bioinformatics and machine learning
doi 10.3389/fmed.2024.1309510
- 1,165 views
- 1 citation
ORIGINAL RESEARCH
Published on 13 Feb 2024
Association between visceral fat area and diabetic retinopathy among people with type 2 diabetes mellitus: a cross-sectional study in Ningbo, Zhejiang Province, China
doi 10.3389/fmed.2024.1327805
- 1,161 views
ORIGINAL RESEARCH
Published on 15 Jan 2024
Adult-onset neuronal intranuclear inclusion disease related retinal degeneration: a Chinese case series
doi 10.3389/fmed.2024.1188193
- 1,172 views
ORIGINAL RESEARCH
Published on 09 Jan 2024
Unlocking therapeutic potential: dual gene therapy for ameliorating the disease phenotypes in a mouse model of RPE65 Leber congenital amaurosis
doi 10.3389/fmed.2023.1291795
- 1,445 views
- 2 citations
MINI REVIEW
Published on 01 Dec 2023
Adeno-associated virus vectors for retinal gene therapy in basic research and clinical studies
doi 10.3389/fmed.2023.1310050
- 3,947 views
- 6 citations
ORIGINAL RESEARCH
Published on 12 Oct 2023
Pathogenicity and functional analysis of CFAP410 mutations causing cone-rod dystrophy with macular staphyloma
doi 10.3389/fmed.2023.1216427
- 1,892 views
- 2 citations
CASE REPORT
Published on 11 Aug 2023
Case report: Familial foveal retinoschisis caused by CRB1 gene mutation in a family with recessive inheritance
doi 10.3389/fmed.2023.1220075
- 1,428 views
- 1 citation
