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Research 91–120 of 1000+
- Lichen‐planopilaris‐like scarring pattern in a patient with alopecia and pityriasis rubra pilaris
- Overlap Between Ulerythema Ophryogenes and Keratosis Follicularis Spinulosa Decalvans: a Case Report
- Trachyonychia with juvenile pityriasis rubra pilaris
- Keratosis Follicularis Squamosa in Unilateral Buttock: A Case Report and Review of Literature in China
- A Rare Case of Keratosis Follicularis Spinulosa Decalvans Affecting a Female Child
- Frontal fibrosing alopecia and ulerythema ophryogenes as two entites that can transist one into another
- Keratosis follicularis spinulosa decalvans: a family study of seven male cases and six female carriers.
- Stanozolol in the Treatment of Pityriasis Rubra Pilaris
- CuATSM Enhances Wound Repair Without Scarring via Hippo/YAP Signalling Pathway to Reduce Ferroptosis and Macrophage Polarisation
- Primary cicatricial alopecia
- Primary Cicatricial Alopecias
- Primary cicatricial alopecias
- Lichen planopilaris
- Ponatinib-induced pityriasis rubra pilaris-like adnexal dysmaturation: A case report
- Profile of dermatological consultations in Brazil (2018)
- Black women’s hair: the main scalp dermatoses and aesthetic practices in women of African ethnicity
- Controversies in off‐label prescriptions in dermatology: the perspective of the patient, the physician, and the pharmaceutical companies
- A CLINICOEPIDEMIOLOGICAL STUDY OF CUTANEOUS MANIFESTATIONS IN GERIATRIC AGE GROUP
- Uncommon Presentation of Pityriasis Rubra Pilaris of the Scalp: Clinical, Trichoscopic, and Histopathologic Features and Review of the Literature
- SUMMARIES OF PAPERS
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- The clinical features and histopathologic patterns of folliculotropic mycosis fungoides in a series of 38 cases
- Ulerythema ophryogenes with multiple congenital anomalies
- Rare Cutaneous Side Effects of Imiquimod: A Review on Its Mechanisms, Diagnosis, and Management
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Poster Presentations
- Case Report of Wound Treatment with Hyiodine Gel in an Occasional KID Syndrome Patient
- Dermoscopic features of follicular mycosis fungoides of nonscalp areas: Report of 11 cases and literature review
- Medications
- Monilethrix: a typical case report with microscopic and dermatoscopic findings