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Research 31–60 of 1000+
- Is there a role for dermatologists in eating disorders?
- Platelet-rich fibrin in the management of oral mucosal lesions: a scoping review
- An animal study on the effectiveness of platelet-rich plasma as a direct pulp capping agent
- Read-Through for Nonsense Mutations in Type XVII Collagen‒Deficient Junctional Epidermolysis Bullosa
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- 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
- TONGUE, RED
- The dental needs of children with Epidermolysis Bullosa and service delivery: a scoping review
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Comparison of prevalence of periodontal disease in women with polycystic ovary syndrome and healthy controls
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Stabilization of epithelial β-catenin compromises mammary cell fate acquisition and branching morphogenesis
- E-Poster
- Severe Abnormalities in the Oral Mucosa Induced by Suprabasal Expression of Epidermal Keratin K10 in Transgenic Mice
- 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
- Carbon, nitrogen, and sulfur elemental and isotopic variations in mouse hair and bone collagen during short-term graded calorie restriction
- Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa
- Identification of a novel homozygous LAMB3 mutation in a Chinese male with junctional epidermolysis bullosa and severe urethra stenosis: A case report
- Genetic Disorders and Defects in Vitamin D Action
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family