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Research 61–90 of 1000+
- Treating of resistant cases of alopecia universalis
- [Translated article] Trichoscopy: An Update
- Eyelashes: Anatomical and Physiological Features, Eyelash Loss and Trichomegaly: Review
- Clinical Case Notes. Tamoxifen optic neuropathy
- CUTANEOUS SIDE-EFFECTS OF BETA-ADRENERGIC BLOCKERS
- Clinical Case Notes. Intraorbital ophthalmic artery aneurysms
- Organoids and organ chips in ophthalmology
- Recurrent Central Serous Retinopathy with Permanent Visual Loss in a U.S. Naval Fighter Pilot
- Clinical Case Notes. Optical coherence tomography of adult-onset foveomacular vitelliform dystrophy
- Bilateral morphea en coup de sabre: a rare presentationof linear morphea
- Functional lacrimal gland regeneration by transplantation of a bioengineered organ germ
- Delivery of Tissue-Targeted Scalpels: Opportunities and Challenges for <i>In Vivo</i> CRISPR/Cas-Based Genome Editing
- Development and Prospects of Organ Replacement Regenerative Therapy
- Homeostatic maintenance of the murine corneal epithelium in pathophysiological contexts
- Changes in Color of Hair and Feathers
- Androgenic alopecia and its association with metabolic syndrome
- Expression and roles of steroidogenic acute regulatory (StAR) protein in ‘non-classical’, extra-adrenal and extra-gonadal cells and tissues
- Development and validation of the Brigham Eyelash Tool for Alopecia (BELA): A measure of eyelash alopecia areata
- Isolated episcleral plasmacytoma mimicking episcleritis in a patient with benign monoclonal gammopathy
- 461 Identification of a Novel Pathogenic XPC:c.2420+1G>C Variant in a Patient with Xeroderma Pigmentosum
- Surgical Treatment of the Brow and Upper Eyelid
- Taurine, a non-proteinous essential amino acid for human body systems: an overview
- Intraretinal variation in disease severity in the Oat mouse model of gyrate atrophy
- Retinol dehydrogenase 12 (RDH12): Role in vision, retinal disease and future perspectives
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Evaluation of dry eye and Meibomian gland dysfunction in female androgenetic alopecia patients
- DERMATOLOGIC DISEASES AND PROBLEMS OF WOMEN THROUGHOUT THE LIFE CYCLE
- A rare case of complete Vogt-Koyanagi-Harada disease presenting to a tertiary care hospital in late stage: Clinical features, diagnosis, and management
- Vogt-Koyanagi-Harada disease occurring during pegylated interferon-α2b and ribavirin combination therapy for chronic hepatitis C
- Psychocutaneous disease