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Last Updated : 06/20/2022

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Found 12 publications

A Case Report of an Infant with Autosomal Recessive Dystrophic Epidermolysis Bullosa: COL7A1 Gene Mutations at C2005T and G7922A.

Impact of low-dose calcipotriol ointment on wound healing, pruritus and pain in patients with dystrophic epidermolysis bullosa: A randomized, double-blind, placebo-controlled trial.

Wound therapy with cold atmospheric plasma in severe recessive dystrophic epidermolysis bullosa : A pilot study.

Does fludarabine have a beneficial effect in recessive dystrophic epidermolysis bullosa?

Genetic and acquired blistering disorders of pediatric age group: An experience from Eastern India.

A Case of Dominant Dystrophic Epidermolysis Bullosa with a G2043R Mutation in the Type VII Collagen Gene.

Intravenous allogeneic umbilical cord blood-derived mesenchymal stem cell therapy in recessive dystrophic epidermolysis bullosa patients.

Raloxifene and n-Acetylcysteine Ameliorate TGF-Signalling in Fibroblasts from Patients with Recessive Dominant Epidermolysis Bullosa.

Presentation of pleural effusion and dilated cardiomyopathy in a case of dystrophic epidermolysis bullosa.

Promising effect of intravenous immunoglobulin therapy for epidermolysis bullosa pruriginosa.

Phase 1/2a clinical trial of gene-corrected autologous cell therapy for recessive dystrophic epidermolysis bullosa.

Safety and early efficacy outcomes for lentiviral fibroblast gene therapy in recessive dystrophic epidermolysis bullosa.

Showing 1-12 of 12

Last Updated : 06/20/2022