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Research 271–300 of 1000+
- Follicular dysplasia and hair loss in white-tailed deer (<i>Odocoileus virginianus</i>)
- 130 Expression of nidogen1 in basal cell carcinoma
- Demodicidose generalizada em cão da raça Teckel: Relato de caso
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- News in brief
- Androgenetic alopecia in males – characteristics and overview of therapies available in cosmetology and aesthetic medicine clinics
- Montagna Symposium 2017—Precision Dermatology: Next Generation Prevention, Diagnosis, and Treatment
- The microbiome in patients with atopic dermatitis
- Application of mesenchymal stem cells for anti-senescence and clinical challenges
- Trends in the global organoid technology and industry: from organogenesis in a dish to the commercialization of organoids
- Hidradenitis Suppurativa/Acne Inversa/Dissecting Terminal Hair Folliculitis
- Plain Language Summaries
- Trichothiodystrophy: Current Concepts
- Alopecia areata – Current understanding and management
- Essential Oils and Melatonin as Functional Ingredients in Dogs
- Diagnosis of Scalp Disorders using Machine Learning and Deep Learning Approach -- A Review
- A guide to cost-effective emollient prescribing
- Interventions for morphea
- Frontal Fibrosing Alopecia
- Regulatory T cell dysfunction and immunotherapeutic breakthroughs in type 1 diabetes
- The Carcinogenesis of the Human Scalp: An Immunometabolic-Centered View
- PA05 A rare case of cardiocutaneous syndrome in a young child
- Lupus erythematosus: systemic and cutaneous manifestations
- Systematic investigation of a potential epidemiological and genetic association between male androgenetic alopecia and COVID‐19
- Identifying critical cell types and gene regulatory pathways for hair and skin disease
- Integrated single-cell chromatin and transcriptomic analyses of human scalp identify gene-regulatory programs and critical cell types for hair and skin diseases
- Lymphocytes, neuropeptides, and genes involved in alopecia areata
- A missense mutation in Lama3 causes androgen alopecia
- Complete defect in PA-PLA1α secretion function leading to autosomal recessive woolly hair and hypotrichosis: insights from a novel compound heterozygous LIPH variant study in a Chinese pedigree
- Melasma and Endocrine Disorders