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Research 91–120 of 1000+
- Paramedian Forehead Flap Hair Removal: A Comprehensive Review of Techniques, Timing, Challenges, and Future Directions
- Abstracts from the Symposium on the Pathophysiology of Hair Growth Organized by the Institute of Dermatology at the Royal Society of Medicine, 29 October 1987
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- Alopezien und Hypotrichosen im Kindesalter
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Exploring the landscape of hair and scalp disorders in the pediatric skin of color population: A scoping review
- Influence of Extended Photoperiod Using Blue Light Masks on Hypertrichosis, Coat Condition and General Health Parameters in Horses with Pituitary Pars Intermedia Dysfunction
- Highly Prevalent LIPH Founder Mutations Causing Autosomal Recessive Woolly Hair/Hypotrichosis in Japan and the Genotype/Phenotype Correlations
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Complete defect in PA-PLA1α secretion function leading to autosomal recessive woolly hair and hypotrichosis: insights from a novel compound heterozygous LIPH variant study in a Chinese pedigree
- 52993 Regulatory γδ T cells protect human scalp hair follicles from alopecia areata in vivo
- British Hair and Nail Society
- Latanoprost-Loaded Nanotransfersomes Designed for Scalp Administration Enhance Keratinocytes Proliferation
- Hormonal profile and androgen receptor study in prepubertal girls with hypertrichosis
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Bimatoprost in the treatment of eyelash hypotrichosis
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Current standards in the diagnostics and therapy of hair diseases - hair consultation
- Short anagen syndrome
- Therapeutic effects of a new long-acting growth factor cocktail (Cellcurex™) injected using a microneedle on the scalp in patients with androgenetic alopecia: A split study
- Congenital hair loss disorders: Rare, but not too rare
- Hair removal using a long-pulsed alexandrite laser.
- Preparation and evaluation of minoxidil nanoemulgel topical formulations.
- 15. Hair and Nails
- Genetic Hair Disorders: A Review
- Desmogleins: Hair perspective
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Targeted Self-Assembled anti-NFκB AuNCs-Aptamer Nanoplatform for Precise Theranostics via Tailored Follicle Regeneration
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome