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Research 91–120 of 227
- LEKTI: Netherton Syndrome and Atopic Dermatitis
- Ponatinib-induced pityriasis rubra pilaris-like adnexal dysmaturation: A case report
- Kava-induced acute cutaneous toxicity: An increasingly recognized characteristic clinicohistologic pattern
- Trichoscopy in genetic hair shaft abnormalities
- Dupilumab in Inflammatory Skin Diseases: A Systematic Review
- Trichoscopy as a diagnostic tool in trichorrhexis invaginata and Netherton syndrome
- Ingestion of a dietary supplement resulting in selenium toxicity
- Genetic Hair Disorders: A Review
- Poster Presentations
- <i>NIPAL4</i> deletion identified in an American Bully with autosomal recessive congenital ichthyosis and response to topical therapy
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Rickets in association with skin diseases and conditions: A review with emphasis on screening and prevention
- Phenotyping mice with skin, hair, or nail abnormalities: A systematic approach and methodologies from simple to complex
- Positive Impact of Fish Oil on Diabetic and Hypercholestrolemic Skin Disorders
- Case Report of Wound Treatment with Hyiodine Gel in an Occasional KID Syndrome Patient
- Cellular and Metabolic Basis for the Ichthyotic Phenotype in NIPAL4 (Ichthyin)–Deficient Canines
- Hodgkin′s lymphoma presenting as alopecia
- “Structural imprinting” of the cutaneous immune effector function
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- New clinico‐genetic classification of trichothiodystrophy
- Uncommon Presentation of Pityriasis Rubra Pilaris of the Scalp: Clinical, Trichoscopic, and Histopathologic Features and Review of the Literature
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- Cell death by cornification
- Asebia-2J (Scd1ab2J): A New Allele and a Model for Scarring Alopecia
- British Association of Dermatologists guidelines on the efficacy and use of acitretin in dermatology
- Netherton's syndrome: A syndrome of elevated IgE and characteristic skin and hair findings
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation
- An unexpected role for keratin 10 end domains in susceptibility to skin cancer
- Psychological interventions in the management of common skin conditions