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Research 391–420 of 489
- JAK-Inhibitors Beyond the Label: Emerging Applications in Dermatology
- Follicular keratotic diseases: a retrospective study of 50 cases in a tertiary care center of rural South India with dermoscopy and histopathology evaluation
- Review of Promising Off-Label Use of Deucravacitinib
- Netherton Syndrome – Responding to Oral Retinoids
- An Unusual Case of Mycosis Fungoides Presenting with Multiple Atypical Morphologies in a Photoexacerbated Distribution
- Understanding the Intricate Pathophysiology of Psoriasis and Related Skin Disorders
- The Role of Extracellular Vesicles in the Development and Treatment of Psoriasis: Narrative Review
- Navaratnas in Dermatology
- Uncommon Presentation of Pityriasis Rubra Pilaris of the Scalp: Clinical, Trichoscopic, and Histopathologic Features and Review of the Literature
- 1,314
- Viva questions from the IJDVL
- Subject Index
- Update in Dermatology
- Emerging Topical and Systemic JAK Inhibitors in Dermatology
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- The IL-23/IL-17 Pathway in Inflammatory Skin Diseases: From Bench to Bedside
- Proteome Analysis of Human Hair Shaft
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Changing Patterns of Localization of Putative Stem Cells in Developing Human Hair Follicles
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- The molecular basis of human keratin disorders
- Peptidylarginine Deiminase Isoforms Are Differentially Expressed in the Anagen Hair Follicles and Other Human Skin Appendages
- New clinico‐genetic classification of trichothiodystrophy
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- 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
- Primary Follicular Dystrophy With Scarring Dermatitis in C57BL/6 Mouse Substrains Resembles Central Centrifugal Cicatricial Alopecia in Humans
- Loss of epidermal Evi/Wls results in a phenotype resembling psoriasiform dermatitis
- Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13