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Research 601–630 of 1000+
- Delayed epidermal permeability barrier formation and hair follicle aberrations in Inv-Cldn6 mice
- Keratosis Follicularis Spinulosa Decalvans
- The keratins and their disorders
- Trichoscopic features of frontal fibrosing alopecia: Results in 249 patients
- Skin manifestations of obesity: a comparative study
- Dermoscopic Approach to a Small Round to Oval Hairless Patch on the Scalp
- Perifollicular erythema as a trichoscopy sign of progression in frontal fibrosing alopecia
- Role of insulin resistance and diet in acne
- Lichen planopilaris epidemiology: a retrospective study of 80 cases
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Syphilitic alopecia: uncommon trichoscopic findings
- Pathologic Diagnosis of Central Centrifugal Cicatricial Alopecia on Horizontal Sections
- DERMATOLOGIC INVESTIGATION OF ALOPECIA IN RHESUS MACAQUES (MACACA MULATTA)
- Histological and dermatoscopic description of sphynx cat skin
- <i>Malassezia slooffiae</i>‐associated dermatitis in a goat
- Monilethrix treated with the oral retinoid Ro 10-9359 (Tigason)
- Frontal fibrosing alopecia: a case series of 65 patients seen in a single Italian centre
- Recessive Epidermolysis Bullosa Simplex Phenotype Reproduced in Vitro
- Lichen planopilaris in a Latin American (Chilean) population: demographics, clinical profile and treatment experience
- Follicular mycosis fungoides associated with lithium
- Pachyonychia Congenita-Associated Alopecia. A Microscopic Analysis Using Transverse Section Technique
- Follicular ichthyosis
- Keratins: Dynamic, flexible structural proteins of epithelial cells
- Trichostasis Spinulosa
- Trichostasis Spinulosa
- Follicular and perforating disorders
- THERAPEUTIC HOTLINE: Effectiveness of the association of cetirizine and topical steroids in lichen planus pilaris - an open-label clinical trial
- Antigen presenting cells in the skin of a patient with hair loss and systemic lupus erythematosus.
- A four generation hidrotic ectodermal dysplasia family: an allelic variant of Clouston syndrome?
- Skin features in myotonic dystrophy type 1: An observational study