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Research 91–120 of 1000+
- Madarosis: A marker of many Maladies
- Comorbidities and Treatment Options for Acne Keloidalis Nuchae
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Ichthyosis Follicularis With Alopecia and Photophobia
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Trias of keratosis pilaris, ulerythema ophryogenes and 18p monosomy: Zouboulis syndrome
- Combination of tacalcitol ointment and photodynamic therapy for the treatment of follicular mucinosis of the scalp
- The usefulness of dermoscopy in canine pattern alopecia: a descriptive study
- Enhancement of Hair Growth through Stimulation of Dermal Papilla Cells in Human Follicular Dermal
- Erythromelanosis follicularis faciei in women
- Multi-dermatomal unilateral nevus comedonicus along the lines of Blaschko: a rare presentation
- Dermoscopy: A rapid bedside tool to assess monilethrix
- Kératose pilaire
- Ichthyosis follicularis alopecia and photophobia syndrome:Transient improvement with oral isotretinoin
- Nilontinib induced keratosis pilaris atrophicans
- Nilotinib-Induced Keratosis Pilaris
- Circle hairs involving the extremities in a young girl
- Graham Little-Piccardi-Lassueur syndrome associated with androgen insensitivity syndrome (testicular feminization)
- Dermoscopic features of discoid lupus erythematosus
- Skin Conditions in Figure Skaters, Ice-Hockey Players and Speed Skaters
- Atrichia with papular lesions
- A case of eruptive lichen spinulosus after toxic epidermal necrolysis
- Ulerythema ophryogenes with multiple congenital anomalies
- Surgical Management of Scarring Alopecia
- Discreet monilethrix: De novo mutation on the example of polish families
- [Cutaneous manifestations of malabsorption diseases (author's transl)].
- The Link Between Obesity and the Skin
- Itchy Black Hair Bristles on Back
- Pigmented Rings With Central Clearing: A Dermoscopic Feature of Melasma
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2