Search
for
Sort by
Research 31–60 of 798
- TONGUE, RED
- Madarosis: A marker of many Maladies
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- Congenital and Hereditary Skin Diseases
- Congenital and Hereditary Skin Diseases
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Skin, Genetic Defects, and Aging
- Secondary Cicatricial and other Permanent Alopecias
- From molecular biology to therapeutics
- Management of congenital ichthyoses: European guidelines of care, part two
- Semidominant Inheritance in Epidermolytic Ichthyosis
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- The Genetics of Human Skin Disease
- New developments in the molecular treatment of ichthyosis: review of the literature
- Dermatopathology and molecular genetics
- Common Dermatologic Disorders in Down Syndrome: Systematic Review
- Gene Therapy: Recent Advances and Applications in Dermatology
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- PHILADELPHIA DERMATOLOGICAL SOCIETY
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- Clinical Snippets
- Keratins and skin disease
- Key Factors in the Complex and Coordinated Network of Skin Keratinization: Their Significance and Involvement in Common Skin Conditions
- Proceedings of the Inaugural Pediatric Dermatology Research Alliance (PeDRA) Conference
- Oral Presentations
- 475 Paraoxonase 1 (PON1) L55M and Q192R polymorphisms, lipid profiles and psoriasis
- 476 Development of an intrinsic skin sensor for blood glucose level with CRISPR-mediated genome editing in epidermal stem cells
- Cushing Syndrome from Percutaneous Absorption of 1% Hydrocortisone Ointment in Netherton Syndrome
- Vitamins