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Research 31–60 of 160
- Dupilumab in a 9-week-old with Netherton Syndrome Leads to Deep Symptom Control
- Genetic Susceptibility to Alopecia
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Abstracts Pt.30
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
- KLK5 and KLK7 Ablation Fully Rescues Lethality of Netherton Syndrome-Like Phenotype
- Dermatoscopy of hair shaft disorders
- Dissecting the microenvironment around biosynthetic scaffolds in murine skin wound healing
- Management of congenital ichthyoses: European guidelines of care, part two
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Congenital hair loss disorders: Rare, but not too rare
- Trichoscopy in Hair Shaft Disorders
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Hair Loss in Children
- The Genetics of Human Skin Disease
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Skin transcriptome profiling of Changthangi goats highlights the relevance of genes involved in Pashmina production
- Establishment of keratinocyte cell lines from human hair follicles
- Evolving approaches to profiling the microbiome in skin disease
- Hair loss and its management in children
- Advances in Hair Diseases
- Atopic dermatitis and risk of autoimmune diseases: a systematic review and meta-analysis
- Inherited Disorders of the Hair
- Trichodystrophies: A hair-raising differential diagnosis
- Hair loss in infancy and childhood
- Clinical Manifestation and Classification of Japanese patients with Inherited Keratinizing Disorders
- Enhanced Differentiation Potential of Pigmented Human Epidermal Equivalents
- Regenerative potential of CD200- subpopulations of hair follicle bulge
- Hair shaft disorders