Related Experiment Videos

The management of dystrophic epidermolysis bullosa

M G Dunnill¹, R A Eady

¹St John's Institute of Dermatology, St Thomas' Hospital, London, UK.

Clinical and Experimental Dermatology

|May 1, 1995

Abstract

No abstract available in PubMed .

Related Concept Videos

Articles linked to this work by shared authors, journal, and citation graph.

Epidermolysis bullosa: scientific advances and therapeutic challenges.

The Journal of dermatology·2002

New mutations in keratin 1 that cause bullous congenital ichthyosiform erythroderma and keratin 2e that cause ichthyosis bullosa of Siemens.

The British journal of dermatology·2001

A comparison of different lysis buffers to assess allele dropout from single cells for preimplantation genetic diagnosis.

Prenatal diagnosis·2001

Spectrum of dominant mutations in the desmosomal cadherin desmoglein 1, causing the skin disease striate palmoplantar keratoderma.

European journal of human genetics : EJHG·2001

Novel splice site mutation in keratin 1 underlies mild epidermolytic palmoplantar keratoderma in three kindreds.

The Journal of investigative dermatology·2001

Three cases of de novo dominant dystrophic epidermolysis bullosa associated with the mutation G2043R in COL7A1.

Clinical and experimental dermatology·2001

See all related articles