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Research 781–810 of 1000+
- Intraretinal variation in disease severity in the Oat mouse model of gyrate atrophy
- Pharmacological BACE1 and BACE2 inhibition induces hair depigmentation by inhibiting PMEL17 processing in mice
- Preliminary toxicity profile of arotinoids SMR-2 and SMR-6 in male B6D2F1 mice*1
- 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
- FINASTERIDE FOR CHRONIC CENTRAL SEROUS CHORIORETINOPATHY
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- A woman with headaches and blurred vision
- Microscopic polyangiitis secondary to Mycobacterium abscessus in a patient with bronchiectasis: a case report
- Organ Regeneration
- 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
- Cutaneous lupus erythematosus
- 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
- 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
- Abstracts
- Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy
- Clinical case of Vogt–Koyanagi–Harada syndrome