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Research 391–420 of 1000+
- Alopecia Areata: Why is it Areata?
- Monitoring chemotherapy‐induced alopecia with trichoscopy
- Anagen effluvium
- Efluvio anágeno. Hallazgos tricoscópicos
- Alopecia areata: Clinical presentation, diagnosis, and unusual cases
- ‘Follicular Swiss cheese’ pattern - another histopathologic clue to alopecia areata
- Telogen Effluvium Caused by Magnesium Valproate and Lamotrigine
- Molecular Genetics of Alopecias
- Scalp Sarcoidosis with Systemic Involvement: A Case Report and Literature Review
- Morphological changes in the skin in a rat model of stress-induced alopecia and their correction with nutrients
- Regenerative Cosmetics: Skin Tissue Engineering for Anti-Aging, Repair, and Hair Restoration
- The Biology and Genomics of Human Hair Follicles: A Focus on Androgenetic Alopecia
- Safety and efficacy of hair growth promoting product in adult human subject having hair fall complaints (alopecia)
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- Scalp Psoriasis
- Vitamins
- Female-patterned alopecia in teenage brothers with unusual histologic features
- Hydroxyl radical mediates cisplatin-induced apoptosis in human hair follicle dermal papilla cells and keratinocytes through Bcl-2-dependent mechanism
- Skin Manifestations in Primary Immunodeficient Children
- Obsessive-compulsive disorder in dermatology
- A rare case of woolly hair with unusual associations
- ACUTE ZINC DEPLETION SYNDROME DURING PARENTERAL HYPERALIMENTATION
- [Evaluation of vitamin B6 and calcium pantothenate effectiveness on hair growth from clinical and trichographic aspects for treatment of diffuse alopecia in women].
- Proteomics demonstration that histone H4 is a colchicine-induced retro-modulator of growth and alkaline phosphatase activity in hair follicle dermal papilla culture
- Women's Dermatologic Diseases, Health Care Delivery, and Socioeconomic Barriers
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- Biotin
- A Case of Hemi‐Isaac's Syndrome
- Cronkhite-Canada syndrome: A rare disease presenting with dermatological and gastrointestinal manifestations
- Dermatological manifestations and associated factors in patients with Graves\' disease in Dakar