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Research 31–60 of 237
- Is there a role for dermatologists in eating disorders?
- An animal study on the effectiveness of platelet-rich plasma as a direct pulp capping agent
- General Dermatology
- Cutaneous manifestations of systemic infection in children
- Long-term complications of Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS/TEN): the spectrum of chronic problems in patients who survive an episode of SJS/TEN necessitates multidisciplinary follow-up
- TGF-β Family Signaling in Epithelial Differentiation and Epithelial–Mesenchymal Transition
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Oral Manifestations of Hematologic and Nutritional Diseases
- Fibromodulin-Deficiency Alters Temporospatial Expression Patterns of Transforming Growth Factor-β Ligands and Receptors during Adult Mouse Skin Wound Healing
- Light emitting diodes technology-based photobiomodulation therapy (PBMT) for dermatology and aesthetics: Recent applications, challenges, and perspectives
- Potential Health Benefit of Dates Based on Human Intervention Studies: A Brief Overview
- Acne in children
- Micronutrients for Hair and Nails
- Cytostatics and immunosuppressive drugs
- Read-Through for Nonsense Mutations in Type XVII Collagen‒Deficient Junctional Epidermolysis Bullosa
- TONGUE, RED
- The Autoimmune Regulator (AIRE), Which Is Defective in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy Patients, Is Expressed in Human Epidermal and Follicular Keratinocytes and Associates With the Intermediate Filament Protein Cytokeratin 17
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Androgen Levels and Body Size Are Associated with Directional as Well as Fluctuating Asymmetry Patterns in Adult !Kung San and Kavango Males from Northern Namibia
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Genotype-Phenotype Delineation of Autoimmune Polyendocrinopathy, Candidiasis, and Ectodermal Dystrophy in a Pediatric Patient: A Case Report
- G338(P) Dermatological manifestations in children with chronic kidney disease in a tertiary care center: a case-control study
- A decade of neglecting sublingual mass: A case report of epidermoid cyst
- The dental needs of children with Epidermolysis Bullosa and service delivery: a scoping review
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- Stem Cell Therapies for Epidermolysis Bullosa Treatment
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- Update to acne vulgaris treatment for Canadian practice