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- 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
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