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Research 121–150 of 1000+
- Alopezien und Hypotrichosen im Kindesalter
- Black women’s hair: the main scalp dermatoses and aesthetic practices in women of African ethnicity
- Hair shaft miniaturization causes stem cell depletion through mechanosensory signals mediated by a Piezo1-calcium-TNF-α axis
- [Wooly hair syndrome. Clinical and microscopic study].
- Molecular Basis of Hereditary Hair Diseases
- Promising alternative clinical uses of prostaglandin F2α analogs: Beyond the eyelashes
- The Genetics of Human Skin Disease
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Targeted Self-Assembled anti-NFκB AuNCs-Aptamer Nanoplatform for Precise Theranostics via Tailored Follicle Regeneration
- Risk associated with the use of 5-alpha reductase inhibitors with minoxidil in treatment of male androgenetic alopecia – literature review
- From Eye Care to Hair Growth: Bimatoprost
- Desmogleins: Hair perspective
- Genetic Hair Disorders: A Review
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Current Genetics in Hair Diseases
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Hair Loss in Children
- Hair and Nail Relationship
- Eyelash Trichomegaly: A Rare Presenting Feature of Systemic Lupus Erythematosus.
- Poliosis circumscripta: Overview and underlying causes
- Male fertility and skin diseases
- An Update on Drug-Induced Pigmentation
- Hair Shaft Dysplasias
- Hair loss and its management in children
- Solitary Basaloid Follicular Hamartoma: A Report of Two Cases.
- JOHNE'S AND CROHN'S
- Madarosis, milphosis, eyelash trichomegaly, and dermatochalasis
- Assessment and Validity of Trichoscopy for Eyebrow Involvement in Lichen Planopilaris: A Case-Control Study
- Cyclosporine-induced alopecia:a case report, FDA adverse event reporting system analysis and literature assessment
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population