Otorhinolaryngological and esophageal manifestations of epidermolysis bullosa

Author:

Fantauzzi Rodrigo Santana,Maia Mariana Oliveira,Cunha Flávia Coelho,Simões Rodrigo Vidal,Gonçalves Denise Utsch,Maia Amélio Ferreira

Publisher

Elsevier BV

Subject

Otorhinolaryngology

Reference18 articles.

1. A novel autosomal partially dominant mutation designated G476D in the Keratin 5 gene causing Eidermolysis Bullosa simlex Weber-Cockayne type: A family study with a genetic twist;Kowalewski;Int J Mol Med,2007

2. Genetic abnormalities and clinical classification of Epidermolysis Bullosa;Mitsuhashi;Arch Dermatol Res,2003

3. Inherited epidermolysis bullosa comes into the new millennium: A revised classification system based on current knowledge of pathogenetic mechanisms and the clinical, laboratory, and epidemiologic findings of large, well-defined patients cohorts;Fine;J Am Acad Dermatol,2000

4. Revised classification system for inherited epidermolysis bullosa;Bauer;J Am Acad Dermatol,2000

5. Bullous Eruptions;Wojonarowska,1998

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