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Research 181–210 of 1000+
- Short histological kaleidoscope – recent findings in histology. Part IV
- Editorial highlights
- Primary Vitreoretinal Lymphoma Presenting Solely with Asymptomatic Peripheral Drusenoid Lesions
- Lupus Nephritis with Visual Field Defect Secondary to Hypertensive Retinopathy: A Case Report
- Mimicking Senescence Factors to Characterize the Mechanisms Responsible for Hair Regression and Hair Loss: An In Vitro Study
- FINASTERIDE FOR CHRONIC CENTRAL SEROUS CHORIORETINOPATHY
- Acute central serous chorioretinopathy after prolonged application of topical minoxidil: A case report and review of the literature
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Atualização em Coriorretinopatia Serosa Central
- A woman with headaches and blurred vision
- Frizzled Receptors in Development and Disease
- Microscopic polyangiitis secondary to Mycobacterium abscessus in a patient with bronchiectasis: a case report
- Organ Regeneration
- LHX2: a transcription factor in development, homeostasis, repair, and disease
- Administration of dutasteride in animal models of retinitis pigmentosa
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Organoids and organ chips in ophthalmology
- Finasteride is effective for the treatment of central serous chorioretinopathy
- 869 AN EVALUATION OF ZINC STATUS IN PATIENTS WITH ANOREXIA NERVOSA
- Hair removal by lasers and intense pulsed light sources
- TGF-β Family Signaling in Epithelial Differentiation and Epithelial–Mesenchymal Transition
- Autoimmune Polyglandular Syndrome Type 1 in Russian Patients: Clinical Variants and Autoimmune Regulator Mutations
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Sjogren-Larsson syndrome
- SOX9 in organogenesis: shared and unique transcriptional functions
- Vogt-Koyanagi-Harada Disease: A Narrative Review
- POPPER MACULOPATHY: LONG-TERM FOLLOW-UP AND CASE SERIES
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- Hypotrichosis with juvenile macular dystrophy
- An Australian family with macular dystrophy linked to autosomal recessive alopecia universalis