Disease: Epidermolysis bullosa inversa dystrophica
- Anchoring fibrils, collagen VII, and neutral metalloproteases in recessive dystrophic epidermolysis bullosa inversa
- Characterization of mutant type VII collagens underlying the inversa subtype of recessive dystrophic epidermolysis bullosa
- Dystrophic Epidermolysis Bullosa Inversa - Case Report and Review of the Literature
- Dystrophic epidermolysis bullosa inversa with COL7A1 mutations and absence of GDA-J/F3 protein
- Dystrophic epidermolysis bullosa inversa: a case report
- Dystrophic epidermolysis bullosa inversa: report of two cases with further correlation between electron microscopic and immunofluorescence studies
- Epidermolysis bullosa dystrophica inversa in a child
- Epidermolysis bullosa dystrophica inversa, a review and case report
- Epidermolysis Bullosa Dystrophica Inversa: Case Report of a Novel Genetic Mutation, Involving a Rare Genodermatoses
- Epidermolysis bullosa dystrophica inversa: report on 2 sisters
- Establishing an appropriate level of vitamin D supplementation in paediatric patients with recessive dystrophic epidermolysis bullosa
- Evidence for a structural abnormality of collagen VII in a patient with dystrophic epidermolysis bullosa inversa
- Genotype-phenotype correlation in italian patients with dystrophic epidermolysis bullosa
- Inversa dystrophic epidermolysis bullosa is caused by missense mutations at specific positions of the collagenic domain of collagen type VII
- Itch in recessive dystrophic epidermolysis bullosa: findings of PEBLES, a prospective register study
- Late-onset inversa recessive dystrophic epidermolysis bullosa caused by glycine substitutions in collagen type VII
- Neonatal retention of type VII collagen, transient bullous dermolysis of the newborn and recessive epidermolysis bullosa dystrophica inversa
- Oral involvement of recessive dystrophic epidermolysis bullosa inversa
- Otological complications in inversa type recessive dystrophic epidermolysis bullosa
- Phenytoin therapy in recessive dystrophic epidermolyses (epidermolysis bullosa dystrophica type Hallopeau-Siemens and epidermolysis bullosa dystrophica inversa)
- Pregnancy after PGD for recessive dystrophic epidermolysis bullosa inversa: genetics and preimplantation genetics
- Recessive dystrophic epidermolysis bullosa: presentation of two forms
- Recurrent nonsense mutations within the type VII collagen gene in patients with severe recessive dystrophic epidermolysis bullosa
- The effectiveness of phenytoin in the treatment of epidermolysis bullosa hereditaria dystrophica partim inversa (Gedde-Dahl)
- The first COL7A1 mutation survey in a large Spanish dystrophic epidermolysis bullosa cohort: c.6527insC disclosed as an unusually recurrent mutation
- The inversa type of recessive dystrophic epidermolysis bullosa is caused by specific arginine and glycine substitutions in type VII collagen
- Type VII collagen and 19-DEJ-1 antigen. Comparison of expression in inversa and generalized variants of recessive dystrophic epidermolysis bullosa