Disease: Epidermolysis bullosa- dermolytic
- A case of pretibial dystrophic epidermolysis bullosa: decreased expression of the non-helical domain of type VII collagen molecule
- Acquired epidermolysis bullosa (acquired dermolytic bullous dermatoses) (study of 2 patients)
- Acquired epidermolysis bullosa. A clinico-pathologic study
- Animal model for dermolytic mechanobullous disease: sheep with recessive dystrophic epidermolysis bullosa lack collagen VII
- Antenatal diagnosis of recessive dystrophic epidermolysis bullosa: collagenase expression in cultured fibroblasts as a biochemical marker
- Atypical epidermolysis bullosa simplex with a missense keratin 14 mutation p.Arg125Cys
- Clinicopathologic types of epidermolysis bullosa and their nondermatological complications
- Dermolytic (dystrophic) epidermolysis bullosa inversa
- Dominant dystrophic epidermolysis bullosa of Cockayne-Touraine in father and son: clinical and ultrastructural similarities
- Dystrophic epidermolysis bullosa inversa with COL7A1 mutations and absence of GDA-J/F3 protein
- Dystrophic epidermolysis bullosa with toe nail deformities--report of a case in Benin City, Nigeria
- Eosinophilic infiltrates in epidermolysis bullosa
- Epidermolysis bullosa
- Epidermolysis bullosa acquisita of the immunopathological type (dermolytic pemphigoid)
- Epidermolysis bullosa acquisita with electron microscopical studies
- Epidermolysis bullosa acquisita--manifestations in otorhinolaryngology
- Epidermolysis bullosa acquisita: diagnosis by optic immunofluorescent demonstration of junctional antigens and vitamin E treatment
- Epidermolysis bullosa dystrophica (dermolytic bullous dermatosis)
- Epidermolysis bullosa dystrophica inversa in a child
- Epidermolysis bullosa in the eastern province of Saudi Arabia
- Epidermolysis bullosa letalis with pyloric atresia in an infant
- Epidermolysis bullosa: a review
- Exclusion of linkage between the collagenase gene and generalized recessive dystrophic epidermolysis bullosa phenotype
- Generalized epidermolysis bullosa with congenital synechiae, associated malformations and unusual ultrastructure: a new entity?
- Hereditary blistering disorders
- Human skin collagenase in recessive dystrophic epidermolysis bullosa. Purification of a mutant enzyme from fibroblast cultures
- Immunofluorescence antigen mapping for hereditary epidermolysis bullosa
- Immunofluorescence mapping of antigenic determinants within the dermal-epidermal junction in the mechanobullous diseases
- Immunohistological localization of three basement membrane components in various forms of epidermolysis bullosa
- Inherited epidermolysis bullosa: new diagnostic criteria and classification
- Junctional blisters in acquired bullous disorders of the dermal-epidermal junction zone: role of the lamina lucida as the mechanical locus minoris resistentiae
- Ketamine anesthesia in dermolytic bullous dermatosis (epidermolysis bullosa)
- Letter: Vitamin E treatment of dermolytic bullous dermatoses
- Letter: Vitamin E treatment of dermolytic bullous dermatosis
- Mucosal morbidity in patients with epidermolysis bullosa acquisita
- Treatment of epidermolysis bullosa acquisita with the humanized anti-Tac mAb daclizumab
- Treatment of hand deformities in a long-term survivor with dermolytic bullous dermatosis-recessive (DBD-R)
- Ultrastructural studies in epidermolysis bullosa hereditaria. II. Dominant dystrophic type of Cockayne and Touraine
- Ultrastructural studies in epidermolysis bullosa hereditaria. III. Recessive dystrophic types with dermolytic blistering (Hallopeau-Siemens types and inverse type)
- Vitamin A and vitamin E in dermatology
- Vitamin E treatment of dermolytic bullous dermatosis: a controlled study