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Research 61–90 of 788
- Ichthyosis with confetti: clinics, molecular genetics and management
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Dermatopathology and molecular genetics
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Drug-Induced Hair Loss and Hair Growth
- Differential expression and functionality of ATP-binding cassette transporters in the human hair follicle
- Adverse Dermatologic Effects of Cardiovascular Drug Therapy: Part III
- A guide to diagnosis and management of hypertrichosis
- Severe Skin Permeability Barrier Dysfunction in Knockout Mice Deficient in a Fatty Acid ω-Hydroxylase Crucial to Acylceramide Production
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Ectodermal Dysplasia: Variable Expressions
- Genetic Hair Disorders: A Review
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Circle Hairs in a Patient with Multiple Myeloma
- Congenital hair loss disorders: Rare, but not too rare
- New clinico‐genetic classification of trichothiodystrophy
- Localisation and regulation of cholesterol transporters in the human hair follicle: mapping changes across the hair cycle
- Successful induction of oral tolerance in Netherton syndrome
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Hair Shaft Dysplasias
- Improvement in Hair Loss and Better Hair Quality with Vitamin Therapy in Monilethrix
- SCALP HAIR CHARACTERISTICS IN THE NEWBORN INFANT
- Role of trichoscopy in diagnosis of different hair and scalp disorders in pediatrics
- Thyroid hormone action on skin.
- The Transmembrane Serine Protease HAT-like 4 Is Important for Epidermal Barrier Function to Prevent Body Fluid Loss
- KLK5 and KLK7 Ablation Fully Rescues Lethality of Netherton Syndrome-Like Phenotype
- DRUG‐ASSOCIATED ALOPECIA
- Short anagen syndrome