Jouni Uitto

The classification of inherited epidermolysis bullosa (EB): Report of the Third International Consensus Meeting on Diagnosis and Classification of EB

Inherited epidermolysis bullosa: Updated recommendations on diagnosis and classification

Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility

Intrinsic aging vs. photoaging: a comparative histopathological, immunohistochemical, and ultrastructural study of skin

Targeted Disruption of the Pemphigus Vulgaris Antigen (Desmoglein 3) Gene in Mice Causes Loss of Keratinocyte Cell Adhesion with a Phenotype Similar to Pemphigus Vulgaris

Keloids: The paradigm of skin fibrosis — Pathomechanisms and treatment

Revised classification system for inherited epidermolysis bullosa

Pseudoxanthoma elasticum: Mutations in the <i>MRP6</i> gene encoding a transmembrane ATP-binding cassette (ABC) transporter

Plectin deficiency results in muscular dystrophy with epidermolysis bullosa

Integrin β4 mutations associated with junctional epidermolysis bullosa with pyloric atresia

Missense Mutations in GJB2 Encoding Connexin-26 Cause the Ectodermal Dysplasia Keratitis-Ichthyosis-Deafness Syndrome

Mutations in the 180–kD bullous pemphigoid antigen (BPAG2), a hemidesmosomal transmembrane collagen (COL17A1), in generalized atrophic benign epidermolysis bullosa