Latest Research in Ocular Diseases and Behçet’s Syndrome
89 research papers · 2026 median publication year
Top Research Topics in Ocular Diseases and Behçet’s Syndrome
- Ocular Diseases and Behçet’s Syndrome — 17 papers
- Retinal Development and Disorders — 9 papers
- Ophthalmology and Eye Disorders — 9 papers
- Ocular Oncology and Treatments — 8 papers
- Connective tissue disorders research — 3 papers
- Autoimmune Neurological Disorders and Treatments — 3 papers
- Mitochondrial Function and Pathology — 2 papers
- Multiple Sclerosis Research Studies — 2 papers
- Ocular Disorders and Treatments — 2 papers
- Retinal and Macular Surgery — 2 papers
Highest-Cited Papers
- Bilateral Vaso-Occlusive Retinopathy Unmasking Primary Antiphospholipid Syndrome in a Child
- Biologic Therapy in Refractory Non-Infectious Uveitis: An Analysis of 60 Cases at a Tertiary Eye Care Centre from South India
- Tapetal-like reflex in RPGR-associated retinal dystrophies: two cases with distinct phenotypes
- Late onset LHON: report of two cases with successful recovery of vision
- Optic disc melanocytoma associated with epiretinal membrane: a 5-year follow-up case report
- Ophthalmological and epidemiological profiles of Brazilian patients with philadelphia-negative Myeloproliferative neoplasms
- Comparative Risk of Uveitis with Bisphosphonate Use in Osteoporosis: A Population-Based Cohort Study Using the TriNetX US Database
- Isolated rod-cone dystrophy in homozygous IFT140 missense allele p.Tyr923Asp
- Prevalence and penetrance of heritable retinoblastoma in two adult population cohorts: implications for genomic newborn screening
- Spontaneous Retrobulbar Hematoma During a Hypertensive Crisis Managed Without Surgical Decompression: A Case Report
- Red Eyes Refractory to Corticosteroids
- A case of hypertensive retinopathy developing during pembrolizumab treatment for intrahepatic cholangiocarcinoma
- Opsoclonus in Pediatric Patients: Differential Diagnosis and a Practical Approach to Evaluation
- Unilateral Fibrovascular Vitreoretinal Proliferation Associated With Retinal Astrocytic Hamartoma Revealing Tuberous Sclerosis Complex in Adulthood
- Early recognition and systemic management of retinal vasculitis in a 15-year-old male
- From Somatic Driver to Molecular Therapy in Retinal, Choroidal and Periocular Vascular Disease: Mosaicism, Targetable Pathways and Ocular Toxicity
- Charting the Phenotypic Landscape of FBN1 Variants in Marfan Syndrome With Ectopia Lentis Through Extreme Phenotype Sampling
- A case of multiple evanescent white dot syndrome as epiphenomenon of cytomegalovirus infection
- Biallelic RDH11 variants cause syndromic retinitis pigmentosa with early-onset cataracts and neurodevelopmental delay: a multicenter case series
- Establishment and characterization of primary retinoblastoma cell lines: a comprehensive molecular profiling approach