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Research 61–90 of 969
- The effect of menopause on the skin and other connective tissues
- Black women’s hair: the main scalp dermatoses and aesthetic practices in women of African ethnicity
- Hair Shaft Fracture in a Young Athlete: A Rare Case Report of Acquired Trichorrhexis Nodosa
- Management of congenital ichthyoses: European guidelines of care, part two
- Diagnostic challenges in determining alopecia areata
- Analysis of Chemical Components in Cosmetics and Their Effects on Human Health and Controversies
- Dermatological history and examination
- Nonscarring Alopecias
- Monilethrix: a typical case report with microscopic and dermatoscopic findings
- Dermoscopy: A rapid bedside tool to assess monilethrix
- Generalized atrophic benign epidermolysis bullosa.
- Value of dermoscopy for the diagnosis of monilethrix
- Dysfunction of keratinocyte adhesion
- Alopecia areata in a patient with WNT10A heterozygous ectodermal dysplasia
- Hair Anomalies in a 6-Year-Old Girl
- Discreet monilethrix: De novo mutation on the example of polish families
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Homozygous Nonsense Mutation in DSC3 Resulting in Skin Fragility and Hypotrichosis
- Monilethrix in three generations
- Dermatologic manifestations of thyroid disease: a literature review
- A keratin scaffold regulates epidermal barrier formation, mitochondrial lipid composition, and activity
- Keratins: the hair shaft's backbone revealed
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Keratins and disease at a glance
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Poster Presentations
- Hair shaft disorders in children – An update
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- VIJAYA-The one who fights to win
- Alopecia in a Viable Phospholipase C Delta 1 and Phospholipase C Delta 3 Double Mutant