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Research 211–240 of 1000+
- The Transmembrane Serine Protease HAT-like 4 Is Important for Epidermal Barrier Function to Prevent Body Fluid Loss
- Hair Shaft Dysplasias
- Skin diseases in consequence of endocrine alterations
- Clinical relevance of hair microscopy in alopecia
- Potential Medical Uses of Cannabigerol: A Brief Overview
- Common Dermatologic Conditions
- Association of male pattern baldness with angiographic coronary artery disease severity and collateral development
- Evolving approaches to profiling the microbiome in skin disease
- Multiple minute digitate hyperkeratosis
- Common Baldness in Women
- Disease causing homozygous variants in the human hairless gene
- Associations between sun sensitive pigmentary genes and serum prostate specific antigen levels
- Computational derivation of a molecular framework for hair follicle biology from disease genes
- Early-onset baldness and the risk of aggressive prostate cancer: findings from a case–control study
- Outcomes of Tissue Expander Application for Scalp Reconstruction in Extensive Aplasia Cutis Congenita
- Follicular Unit Hair Transplantation
- Abstracts
- Identification of a Novel Missense Mutation in the Fibroblast Growth Factor 5 Gene Associated with Longhair in the Maine Coon Cat
- Diseases that Affect the Pinna
- Sexually dimorphic sail feathers in the Mandarin duck as a model for lifelong developmental modulation
- HuR ablation destabilizes Foxp3 mRNA and impairs regulatory T cell function, contributing to an autoimmune phenotype
- Causality of Aging Hallmarks
- Progeria (Hutchinson-Gilford Syndrome): Literature Review and Clinical Case
- Hidradenitis Suppurativa/Acne Inversa/Dissecting Terminal Hair Folliculitis
- The Skin and Subcutaneous Tissues
- Hereditary, Congenital, and Acquired Alopecias
- SUMMARIES OF PAPERS
- Premature Hair Graying: Underlying Contributors and Management Approaches - An Updated Literature Review
- Muscle pain in a woman with congenital adrenal hyperplasia due to 21-hydroxylase deficiency resolved with testosterone therapy. A case report with 10 years of follow-up
- Case Report: PTCH1 splice-site mutation and sonidegib treatment in Gorlin-Goltz syndrome: clinical insights from a family case study