Search
for
Sort by
Research 391–420 of 400
- The spectrum of fibrosing alopecias
- Trichoscopy as an essential diagnostic technique for hair and scalp disorders in skin of color: A case-control study
- Telogen Effluvium: Potential causes in Iraq
- Hypotrichosis in a child with olmsted syndrome
- Oral Presentations
- Hair & Cutaneous Development
- Molecular Genetics of Human Hair Diseases
- TONGUE, RED
- The Efficacy and Safety of Dr. SKS Hair Booster Serum (a Cocktail of Micronutrients and Multivitamins) in Adult Males and Females With Androgenetic Alopecia: An Open-Label, Non-randomized, Prospective Study
- Alopecia areata – Aktuelles Verständnis und Management
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Atrichia With Papular Lesions
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- Atrichia with papular lesions in two Pakistani consanguineous families resulting from mutations in the human hairless gene
- Atrichia with papular lesions resulting from a novel homozygous missense mutation in the hairless gene
- Atrichia with papular lesions resulting from mutations in the rhesus macaque (<i>Macaca mulatta</i>) <i>hairless</i> gene
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Atrichia and Papular Lesions: Report of a Case
- A Japanese case of ichthyosis follicularis with atrichia and photophobia syndrome with an MBTPS2 mutation
- Keratoma Hereditaria Mutilans (Vohwinkel's Disease) with Congenital Alopecia Universalis (Atrichia Congenita)
- Atrichia with papular lesions
- Identification of novel mutation in the<i>HR</i>gene responsible for atrichia with papular lesions in a Pakistani family
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Identification of a recurrent nonsense mutation in <i>HR</i> gene responsible for atrichia with papular lesions in two Kashmiri families
- Atrichia with Papular Lesions in a Chinese Family Caused by Novel Compound Heterozygous Mutations and Literature Review
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- Mutation des menschlichen hairless -Gens bei Atrichia universalis
- A Novel Mutation in the<i>MBTPS2</i>Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome
- Atrichia with papular lesions in Syrian siblings exposing global diagnostic challenges in genetic alopecia: A rare case report
- Atrichia congenita with papular lesions: A rare cause of pediatric alopecia