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Research 211–240 of 1000+
- Eruptive vellus hair cyst syndrome or exuberant atypical keratosis pilaris?
- 478 Mutation-specific siRNA Knockdown of GJB2 − Potential gene therapy for Keratitis-ichthyosis-deafness Syndrome
- Pityriasis rubra pilaris
- Viral-associated trichodysplasia spinulosa: a case with electron microscopic and molecular detection of the trichodysplasia spinulosa-associated human polyomavirus
- The clinical features and histopathologic patterns of folliculotropic mycosis fungoides in a series of 38 cases
- Ichthyosis follicularis with alopecia and photophobia in a mother and daughter
- Spiny keratoderma ‐ a demonstration of hair keratin and hair type keratinization
- Ulerythema ophryogenes with multiple congenital anomalies
- Fox-Fordyce Disease
- Weathering of the hairless scalp: a study using skin capacitance imaging and ultraviolet light-enhanced visualization
- Tretinoin Treatment of Fox-Fordyce Disease
- Chloracne: histopathologic findings in one case
- Lichen planopilaris [cicatricial (scarring) alopecia] in a child
- Alopecia Universalis Associated with Cutaneous T Cell Lymphoma
- Yellow dots in trichoscopy: relevance, clinical significance and peculiarities
- Dermoscopy of discoid lupus erythematosus: Report of two cases
- Two familial cases of Olmsted-like syndrome with a G573V mutation of the<i>TRPV3</i>gene
- The Link Between Obesity and the Skin
- A rare case of woolly hair with unusual associations
- Dermoscopy: A rapid bedside tool to assess monilethrix
- TRICHOSTASIS SPINULOSA OR PINSELHAAR
- Punctate Follicular Porokeratosis
- Atrichia with papular lesions
- Traumatic anserine folliculosis
- Follicular porokeratosis: four new cases
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Winer's dilated pore, rare presentation in the external ear canal
- Fox-Fordyce disease. Control with tretinoin cream
- [Basal cell carcinomas of the scalp. Review of 77 patients with 81 tumors].
- Natural course of epidermolysis bullosa simplex with mottled pigmentation in a Japanese family with the p.P25L mutation in <i> KRT 5 </i>