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Research 30 of 751
- Systematized Epidermal Nevus with Epidermolytic Hyperkeratosis Improving with Topical Calcipotriol/Betametasone Dipropionate Combination Ointment
- Recessive Epidermolysis Bullosa Simplex Phenotype Reproduced in Vitro
- Missense mutation Y449H of the K10 gene in a patient with severe epidermolytic ichthyosis
- Case of epidermolytic ichthyosis (bullous congenial ichthyosiform erythroderma) with a novel L157P mutation in KRT10 complicated by hypercalcemia
- Natural course of epidermolysis bullosa simplex with mottled pigmentation in a Japanese family with the p.P25L mutation in <i> KRT 5 </i>
- Superficial Epidermolytic Ichthyosis—Hypertrichosis as a Clue to Diagnosis
- Focal palmoplantar callosities in non-Herlitz junctional epidermolysis bullosa
- Keratins: Dynamic, flexible structural proteins of epithelial cells
- A newborn presenting with congenital blistering
- The keratins and their disorders
- Skin, Genetic Defects, and Aging
- Inherited disorders of the skin in human and mouse: from development to differentiation.
- EBS in Children with De Novo Pathogenic Variants Disturbing Krt14
- Research Snippets
- Key Factors in the Complex and Coordinated Network of Skin Keratinization: Their Significance and Involvement in Common Skin Conditions
- Inherited Epidermolysis Bullosa: A Clinical Case
- Alopecia in Epidermolysis Bullosa
- Scarring Alopecia in Localized Dystrophic Epidermolysis Bullosa: A Case Report and a Scoping Review
- Semidominant Inheritance in Epidermolytic Ichthyosis
- KASUS RECESSIVE DYSTROPHIC EPIDERMOLYSIS BULLOSA-MITIS YANG TERDIAGNOSIS PADA SAAT LANJUT USIA
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- Keratin disorders: from gene to therapy
- The Genetics of Human Skin Disease
- Dermatopathology and molecular genetics
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- Localized Epidermolysis Bullosa Simplex (Weber-Cockayne type)
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Recently Identified Forms of Epidermolysis Bullosa