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Research 211–240 of 905
- 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
- Fox-Fordyce Disease
- Weathering of the hairless scalp: a study using skin capacitance imaging and ultraviolet light-enhanced visualization
- Chloracne: histopathologic findings in one case
- Lichen planopilaris [cicatricial (scarring) alopecia] in a child
- Keratosis Pilaris and Scarring Alopecia
- Alopecia Universalis Associated with Cutaneous T Cell Lymphoma
- (16) The Graham-Little syndrome Follicular keratosis with cicatricial alopecia
- Yellow dots in trichoscopy: relevance, clinical significance and peculiarities
- Dermoscopy of discoid lupus erythematosus: Report of two cases
- Follicular Keratosis of the Chin Treated with 1.24R‐Dihydroxyvitamin D3 Ointment
- Two familial cases of Olmsted-like syndrome with a G573V mutation of the<i>TRPV3</i>gene
- Dermoscopy: A rapid bedside tool to assess monilethrix
- TRICHOSTASIS SPINULOSA OR PINSELHAAR
- Punctate Follicular Porokeratosis
- Atrichia with papular lesions
- Follicular porokeratosis: four new cases
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Optical coherence tomography-assisted diagnosis of follicular keratosis of the chin
- Winer's dilated pore, rare presentation in the external ear canal
- Fox-Fordyce disease. Control with tretinoin cream
- Natural course of epidermolysis bullosa simplex with mottled pigmentation in a Japanese family with the p.P25L mutation in <i> KRT 5 </i>
- Osseous Metaplasia and Mature Bone Formation With Extramedullary Hematopoiesis in Trichilemmal Cyst
- [Basal cell carcinomas of the scalp. Review of 77 patients with 81 tumors].
- Overlap Between Ulerythema Ophryogenes and Keratosis Follicularis Spinulosa Decalvans: a Case Report
- Trichoscopy in alopecias
- Atrichia with papular lesions in Syrian siblings exposing global diagnostic challenges in genetic alopecia: A rare case report
- Early Skin Biopsy in Conradi‐Hünermann‐Happle Syndrome (X‐Linked Dominant Chondrodysplasia Punctata)