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- Building Models for Keratin Disorders
- Focal palmoplantar callosities in non-Herlitz junctional epidermolysis bullosa
- RSPO1-mutated keratinocytes from palmoplantar keratoderma display impaired differentiation, alteration of cell–cell adhesion, EMT-like phenotype and invasiveness properties: implications for squamous cell carcinoma susceptibility in patients with 46XX disorder of sexual development
- DSP c.6310delA p.(Thr2104Glnfs*12) associates with arrhythmogenic cardiomyopathy, increased trabeculation, curly hair, and palmoplantar keratoderma
- The Genetics of Human Skin Disease
- The non-neuronal and nonmuscular effects of botulinum toxin: an opportunity for a deadly molecule to treat disease in the skin and beyond
- Inherited Epidermolysis Bullosa: A Clinical Case
- Keratin disorders: from gene to therapy
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
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