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Research 91–120 of 1000+
- Hypotrichosis in a child with olmsted syndrome
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Porphyria Cutanea Tarda – a Case Report
- Diagnosis and Management of Hair Loss in Pediatric
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- Genetics of Alopecia
- What Do We Know About Hair Growth Induced by Wounding and Its Therapeutic Applications?
- Effects of Hormones and Endocrine Disorders on Hair Growth
- Disorders of hair in infants and children other than alopecia
- Scrotal Rejuvenation
- Lady with Long Eyelashes…!
- Circle Hairs in a Patient with Multiple Myeloma
- Disorders of Hair
- General Characteristics of Hair in Eating Disorders
- 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