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Research 451–480 of 1000+
- 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
- Hypotrichosis with juvenile macular dystrophy
- An Australian family with macular dystrophy linked to autosomal recessive alopecia universalis
- Optical Coherence Tomography Angiography Findings in Polycystic Ovary Syndrome
- Abstracts
- Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy
- Amplitude-guided deep reinforcement learning for semi-supervised layer segmentation
- Ophthalmologic Comorbidities in Alopecia Areata
- Effects of local and systemic medications on eye health: Adverse reactions
- Biomedical applications of organoids in genetic diseases
- Alopecia Induced by Poly-L-Lactic Acid Injection
- Clinical case of Vogt–Koyanagi–Harada syndrome
- Taurine, a non-proteinous essential amino acid for human body systems: an overview
- Photobiomodulation therapy in ophthalmology
- A Preview of Selected Articles
- Veterinary Pharmacology
- Forum
- Acquired pili torti--a structural hair shaft defect in anorexia nervosa.
- Síndrome dos cabelos anágenos frouxos associada à distrofia macular: descrição de uma família
- Stem cells, organoids and their applications for human diseases: Special issue of BMB Reports in 2023
- [A systemic-like disease: chronic vitamin A poisoning].
- Melanocytes: The new Black
- Clinical Case Notes. Optical coherence tomography of adult-onset foveomacular vitelliform dystrophy
- Renal Vitamins
- Oral Retinoids in Dermatology