Thomas Jefferson University

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McGrath, JohnPerson Why?
Uitto, JouniPerson Why?
The epidemiology of epidermolysis bullosa in England and Wales: data from the national epidermolysis bullosa database.Academic Article Why?
Autosomal dominant epidermolysis bullosa simplex exacerbated by hyperkeratotic scabies.Academic Article Why?
Cutaneous Squamous Cell Carcinoma in Epidermolysis Bullosa: a 28-year Retrospective Study.Academic Article Why?
Gluten-sensitive enteropathy in recessive dystrophic epidermolysis bullosa.Academic Article Why?
Itch in recessive dystrophic epidermolysis bullosa: findings of PEBLES, a prospective register study.Academic Article Why?
Mohs micrographic surgery for squamous cell carcinoma associated with epidermolysis bullosa.Academic Article Why?
The missense mutation p.R1303Q in type XVII collagen underlies junctional epidermolysis bullosa resembling Kindler syndrome.Academic Article Why?
Treatment of hereditary epidermolysis bullosa: updates and future prospects.Academic Article Why?
Vitamin C concentrations in patients with epidermolysis bullosa.Academic Article Why?
Epidermolysis bullosa pruriginosa: a case with prominent histopathologic inflammation.Academic Article Why?
Progress in epidermolysis bullosa: from eponyms to molecular genetic classification.Academic Article Why?
The international dystrophic epidermolysis bullosa patient registry: an online database of dystrophic epidermolysis bullosa patients and their COL7A1 mutations.Academic Article Why?
A transient epidermolysis bullosa simplex-like phenotype associated with bexarotene treatment in a G138E KRT5 heterozygote.Academic Article Why?
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