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Research 331–360 of 1000+
- CPC14 Blaschko-linear trichoepitheliomas: unveiling type 1 segmental mosaicism
- Causes and Management of Hypertrichosis
- Epidemiological and investigative study of premature graying of hair in higher secondary and pre-university school children
- Ectodermal Dysplasia: Variable Expressions
- An Autosomal Recessive Woolly Hair/Hypotrichosis Case with LIPH Mutation in a Turkish Patient
- Effectiveness of Exosome Treatment in Androgenetic Alopecia: Outcomes of a Prospective Study
- Case Report: 7 Year-Old Saudi Female with Monilethrix
- Female Androgenetic (?) Alopecia
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- TCF/Lef1-Mediated Control of Lipid Metabolism Regulates Skin Barrier Function
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- Werner′s syndrome
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Uncombable hair syndrome due to maternal uniparental disomy of chromosome 1
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- Uncombable hair syndrome: Observations on response to biotin and occurrence in siblings with ectodermal dysplasia
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Dynamic expression of the zinc-finger transcription factor Trps1 during hair follicle morphogenesis and cycling
- Update on hidradenitis suppurativa: connecting the tracts
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma
- Beyond the Hot Comb: Updates in Epidemiology, Pathogenesis, and Treatment of Central Centrifugal Cicatricial Alopecia from 2011 to 2021
- Use of dermoscopy in the diagnosis of temporal triangular alopecia
- Update on Melasma—Part I: Pathogenesis