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Research 31–60 of 43
- Mechanisms of autophagy and their implications in dermatological disorders
- Combined drug triads for synergic neuroprotection in retinal degeneration
- Unilateral branch retinal artery occlusion in a patient with systemic lupus erythematosus
- Impending central retinal vein occlusion and granulomatous uveitis in a patient with Satoyoshi syndrome
- Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy
- Retinal artery occlusion as a probable idiosyncratic reaction to topical minoxidil: a case report
- Proliferative diabetic retinopathy as onset of type 1 diabetes
- Vitiligo and Its Mimics in Childhood: A Diagnostic Framework for Hypopigmented Disorders
- Short-Term Topical Minoxidil Use Associated with Acute Central Serous Chorioretinopathy: A Case Report
- Efficacy and safety of platelet-rich plasma for acute nonarteritic anterior ischemic optic neuropathy: a prospective cohort study
- Nitroxide pharmaceutical development for age-related degeneration and disease
- Therapeutic Efficacy of Spironolactone for Central Serous Chorioretinopathy
- Atualização em Coriorretinopatia Serosa Central
- Dutasteride/finasteride
- Macular Abnormalities Associated With 5α-Reductase Inhibitor
- Immediate Effect in the Retina and Choroid after 650 nm Low-Level Red Light Therapy in Children
- Clinical Features and Treatment Options of Vogt-Koyanagi-Harada Disease
- Interventions for central serous chorioretinopathy: a network meta-analysis
- Primary Vitreoretinal Lymphoma Presenting Solely with Asymptomatic Peripheral Drusenoid Lesions
- Minoxidil
- Clinical Case Notes. Tamoxifen optic neuropathy
- Hypotrichosis with juvenile macular dystrophy
- Multiple and Recurrent Ocular Manifestations in a Patient of Vogt-Koyanagi-Harada Syndrome
- Clinical Case Notes. Castleman's disease of the lacrimal gland
- Recurrent Central Serous Retinopathy with Permanent Visual Loss in a U.S. Naval Fighter Pilot
- Cystoid macular oedema in uveitis: An unsolved problem
- Vogt-Koyanagi-Harada Disease: A Narrative Review
- Clinical Case Notes. Retinoblastoma, microphthalmia and the chromosome 13q deletion syndrome
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- An Atypical Female Case of Ichthyosis Follicularis, Alopecia, and Photophobia (IFAP) Syndrome with Severe Lower Limb Contractures Requiring Orthopedic Surgery