Epidermolysis bullosa (EB) is an inherited, heterogeneous group of rare genetic dermatoses
characterized by mucocutaneous fragility and blister formation, inducible by often minimal …

Epidermolysis bullosa (EB) is a heterogeneous group of inherited skin disorders determined
by mutations in genes encoding for structural components of the cutaneous basement …

Abstract Treatment of superficial tumors with electrochemotherapy (ECT) has shown a steep
rise over the past decade and indications range from skin cancers to locally advanced or …

Recessive dystrophic epidermolysis bullosa (RDEB) is a rare inherited skin and mucous
membrane fragility disorder complicated by early-onset, highly malignant cutaneous …

Epidermolysis bullosa (EB) is a clinically and genetically heterogeneous group of inherited
blistering diseases that affects~ 500,000 people worldwide. Clinically, individuals with EB …

Epidermolysis bullosa (EB) is a group of rare genetic disorders for which significant progress
has been achieved in the development of molecular therapies in the last few decades. Such …

Epidermolysis bullosa (EB) is the umbrella term for a group of rare inherited skin fragility
disorders caused by mutations in at least 20 different genes. There is no cure for any of the …

Background Inherited epidermolysis bullosa (EB) is a genetic disorder characterized by skin
fragility and unique oral features. Aims To provide (a) a complete review of the oral …

Background Recessive dystrophic epidermolysis bullosa (RDEB) is a hereditary blistering
disorder due to a lack of type VII collagen. At present, treatment is mainly supportive …

Background Inherited epidermolysis bullosa (EB) comprises a highly heterogeneous group
of rare diseases characterized by exacerbated skin and/or mucosal fragility and blister …