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Research 31–60 of 777
- First Symposium of Ichthyosis Experts
- 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
- A new heterozygous frameshift variant in keratin 10 resulting in ichthyosis hystrix in a father and daughter
- Ichthyosis
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Keratin disorders: from gene to therapy
- The Genetics of Human Skin Disease
- Dermatopathology and molecular genetics
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- Recessive Epidermolysis Bullosa Simplex Phenotype Reproduced in Vitro
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- <i>NIPAL4</i> deletion identified in an American Bully with autosomal recessive congenital ichthyosis and response to topical therapy
- Chemotherapy of psoriasis and other skin disorders with oral retinoids
- Oral Retinoids in Dermatology
- Clinical Manifestation and Classification of Japanese patients with Inherited Keratinizing Disorders
- Gene Therapy: Recent Advances and Applications in Dermatology
- Common Dermatologic Disorders in Down Syndrome: Systematic Review
- PHILADELPHIA DERMATOLOGICAL SOCIETY
- Advances in the treatment of autosomal recessive congenital ichthyosis, a look towards the repositioning of drugs
- Cellular and Metabolic Basis for the Ichthyotic Phenotype in NIPAL4 (Ichthyin)–Deficient Canines
- Clinical Snippets
- Keratins and skin disease
- Genes of Congenital Dermatologic Disorders in Dogs—A Review
- Proceedings of the Inaugural Pediatric Dermatology Research Alliance (PeDRA) Conference
- Disorders of Keratinization
- Oral Presentations
- Oral retinoids-present status
- 075 Clinical investigation of JAK inhibitor Tofacitinib in scarring alopecias
- 475 Paraoxonase 1 (PON1) L55M and Q192R polymorphisms, lipid profiles and psoriasis