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Research 121–150 of 1000+
- Skin, Genetic Defects, and Aging
- Key Factors in the Complex and Coordinated Network of Skin Keratinization: Their Significance and Involvement in Common Skin Conditions
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- A rare case of woolly hair with unusual associations
- Ectodermal Dysplasia: Variable Expressions
- Inflammatory Vegetative Lesions of the Perineum: A Rare and Severe Clinical Presentation of Netherton Syndrome
- Cushing Syndrome from Percutaneous Absorption of 1% Hydrocortisone Ointment in Netherton Syndrome
- The oestrogen receptor 2 (<i>ESR2</i>) gene in female-pattern hair loss: replication of association with rs10137185 in German patients
- Localisation and regulation of cholesterol transporters in the human hair follicle: mapping changes across the hair cycle
- Ischemic onycholysis of the hands
- 9. Immunology and Genetics
- DERMATOLOGIC DISEASES AND PROBLEMS OF WOMEN THROUGHOUT THE LIFE CYCLE
- Montagna Symposium 2017—Precision Dermatology: Next Generation Prevention, Diagnosis, and Treatment
- Trichoscopy in Hair Shaft Disorders
- Netherton Syndrome in a 9-Month-Old Child: Unraveling a Complex Dermatologic Disorder
- SCALP HAIR CHARACTERISTICS IN THE NEWBORN INFANT
- Oral Presentations
- Molecular Genetics of Alopecias
- Thyroid hormone action on skin.
- The Transmembrane Serine Protease HAT-like 4 Is Important for Epidermal Barrier Function to Prevent Body Fluid Loss
- Perspectives on Dermatopathology
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- The Genetics of Human Skin Disease
- The Spectrum of Skin Disease Among Indian Children
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
- Fatty acids and related lipid mediators in the regulation of cutaneous inflammation
- Differential expression and functionality of ATP-binding cassette transporters in the human hair follicle
- KLK5 and KLK7 Ablation Fully Rescues Lethality of Netherton Syndrome-Like Phenotype
- Beyond Expectations
- HAIR AND SYSTEMATIC DISEASE