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Research 361–390 of 1000+
- Towards the Development of AgoKirs: New Pharmacological Activators to Study Kir2.x Channel and Target Cardiac Disease
- Off-label uses of retinoids in dermatology
- A rare cutis verticis gyrata secondary to cerebriform intradermal nevus: case report and literature review
- Treatment of lipomas and diffuse lipomatosis with NDYAG 1064 NM laser and their impact on the quality of life
- Global hotspots and trends in Acanthosis nigricans research: A bibliometric and visualized analysis
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- Hair microscopy: an easy adjunct to diagnosis of systemic diseases in children
- Key Factors in the Complex and Coordinated Network of Skin Keratinization: Their Significance and Involvement in Common Skin Conditions
- TRPV3 Ion Channel: From Gene to Pharmacology
- Dercum Disease: Exploratory Therapeutic Approaches in the Absence of Standardized Medical Treatment—A Single Center Case Series
- Vitiligo and Its Mimics in Childhood: A Diagnostic Framework for Hypopigmented Disorders
- EBS in Children with De Novo Pathogenic Variants Disturbing Krt14
- Gastric cancer; actualities and perspectives of early diagnosis and targeted therapy
- Madarosis: A marker of many Maladies
- Epidermal patterning and induction of different hair types during mouse embryonic development
- Subject Index
- Skin Development and Disease: A Molecular Perspective
- Clinical and molecular genetic studies in hereditary hair loss
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- Woolly hair generalizado: caso clínico e revisão da literatura
- Familial congenital generalized hypertrichosis
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex
- Clinical cases of Darier-White follicular dyskeratosis
- The Case | Bilateral kidney tumors and lung cysts
- A 40-Year-Old Woman With Facial Papules and Flank Pain
- Abnormal fingerprints and immigration delay disease
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- An Autosomal Recessive Woolly Hair/Hypotrichosis Case with LIPH Mutation in a Turkish Patient
- Tricorrexis nudosa localizada por aplicación compulsiva de minoxidil