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Research 241–270 of 905
- Skin iconography analysis of traumatic anserine folliculosis: Skin image feature of TAF
- Multifocal alopecia of the scalp, axillae, and body
- Multiple facial atrophic scars in childhood
- Reflectance Confocal Microscopy of Adult Periorificial Dermatitis: A Case Report
- Atrichia With Papular Lesions Confirmed via Genetic Testing: A Case Report
- Widespread and eruptive comedonal lesions with alopecia
- Ichthyosiform Erythroderma, a Multifaceted Syndromic Entity
- Trichoscopy I: Non-Cicatricial Alopecia
- Sparse Hair on the Scalp
- Dissecting Cellulitis of the Scalp
- A rare hair loss in children: Monilethrix
- Moniletherix
- The Effect of Hairless Mutant Gene on The Thymus and Skin Under The C_(57)BL/6 Genetic Background
- BRITISH ASSOCIATION OF DERMATOLOGY.
- CENTRAL STATES DERMATOLOGICAL SOCIETY
- Prioritization of therapy uncertainties in congenital ichthyosis: results from a Priority Setting Partnership
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- Skin Conditions in Figure Skaters, Ice-Hockey Players and Speed Skaters
- Erythromelanosis Follicularis Faciei et Colli: A Case Report
- Cutaneous manifestations of dabrafenib (GSK2118436): a selective inhibitor of mutant BRAF in patients with metastatic melanoma
- Validity of trichoscopy in the diagnosis of primary cicatricial alopecias
- Monilethrix: a keratin hHb6 mutation is co‐dominant with variable expression
- Trichoscopic Findings of Erosive Pustular Dermatosis of the Scalp Associated with Gefitinib
- Porokeratotic Eccrine Duct and Hair Follicle Nevus (PEHFN) Associated with Keratitis-Ichthyosis-Deafness (KID) Syndrome
- A Cross-sectional Descriptive Study of Dermoscopy in various Nail Diseases at a Tertiary Care Center
- Graham‐Little Piccardi Lassueur syndrome and review of the literature
- Trichoscopy of Discoid Lupus Erythematosus in Caucasian Scalp: A Review
- Olmsted syndrome
- Pruritic Hyperkeratotic Facial Papules
- Graham–Little–Piccardi–Lassueur syndrome: case report and systematic review of a rare LPP variant