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Research 601–630 of 1000+
- A rare cutis verticis gyrata secondary to cerebriform intradermal nevus: case report and literature review
- Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families
- Ulerythema Ophryogenes in a Saudi Male: A Case Report
- Ruxolitinib Rescues Multiorgan Clinical Autoimmunity in Patients with APS-1
- Shock: A possible presenting manifestation of autoimmune polyendocrine syndrome type II
- Deficient anterior pituitary with common variable immune deficiency (DAVID syndrome): a new case and literature reports
- Generalized Asymptomatic Cutaneous Pits and Comedones in a Young Woman
- An Unusual Case of Diarrhea, Dysgeusia, and Grainy and Nodular Mucosa
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- A Signature of Genes Featuring FGF11 Revealed Aberrant Fibroblast Activation and Immune Infiltration Properties in Keloid Tissue
- Recently Identified Forms of Epidermolysis Bullosa
- Cellular and Metabolic Basis for the Ichthyotic Phenotype in NIPAL4 (Ichthyin)–Deficient Canines
- The systemic wrinkled skin phenotype involves aberrant expression and variation of genes related to the oxidative stress and extracellular matrix in Xiang pigs
- Monilethrix in pattern distribution in siblings: Diagnosis by trichoscopy
- Risk factors and comorbidities associated with central centrifugal cicatricial alopecia
- Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
- Folliculin, the Product of the Birt-Hogg-Dube Tumor Suppressor Gene, Interacts with the Adherens Junction Protein p0071 to Regulate Cell-Cell Adhesion
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- Off-Label Use of Botulinum Toxin in Dermatology—Current State of the Art
- Roux-en-Y gastric bypass in the treatment of non-classic congenital adrenal hyperplasia due to 11-hydroxylase deficiency
- Exosome-based Therapies for Androgenetic Alopecia: Mechanisms, MicroRNAs, and Clinical Prospects
- Pilomatricoma in Syndromic Contexts: A Literature Review and a Report of a Case in Apert Syndrome
- Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan
- Highlights from the 68th Annual Meeting of the Society of Investigative Dermatology
- Metabolic pathways of eicosanoids—derivatives of arachidonic acid and their significance in skin
- Evaluation of Olive Oil-Based Formulations Loaded with Baricitinib for Topical Treatment of Alopecia Areata
- Pathogenesis of androgenetic alopecia
- Wnt/β-catenin signalling: function, biological mechanisms, and therapeutic opportunities
- Central Centrifugal Cicatricial Alopecia: New Insights and a Call for Action
- Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia