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Research 91–120 of 230
- “Structural imprinting” of the cutaneous immune effector function
- Off-label dermatologic uses of IL-23 inhibitors
- Kava-induced acute cutaneous toxicity: An increasingly recognized characteristic clinicohistologic pattern
- Netherton Syndrome – Responding to Oral Retinoids
- “Degeneration” in Dermatopathology
- Kaposi varicelliform eruption
- Cellular and Metabolic Basis for the Ichthyotic Phenotype in NIPAL4 (Ichthyin)–Deficient Canines
- Pigmentary Puzzle: A Rare Case of Hyperpigmented Cutaneous Sarcoidosis
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Trichoscopy as a diagnostic tool in trichorrhexis invaginata and Netherton syndrome
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- A rare complication of follicular hair unit extraction: Kaposi’s varicelliform eruption
- Positive Impact of Fish Oil on Diabetic and Hypercholestrolemic Skin Disorders
- An Unusual Case of Mycosis Fungoides Presenting with Multiple Atypical Morphologies in a Photoexacerbated Distribution
- Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosis
- Advances in the treatment of autosomal recessive congenital ichthyosis, a look towards the repositioning of drugs
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- Asebia-2J (Scd1ab2J): A New Allele and a Model for Scarring Alopecia
- Genetically modified laboratory mice with sebaceous glands abnormalities
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Hair follicles modulate skin barrier function
- Cell death by cornification
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- British Association of Dermatologists guidelines on the efficacy and use of acitretin in dermatology
- A keratin scaffold regulates epidermal barrier formation, mitochondrial lipid composition, and activity
- Trichoscopy in genetic hair shaft abnormalities
- New clinico‐genetic classification of trichothiodystrophy
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation
- Psychological interventions in the management of common skin conditions