Update on diagnosis and therapy of inherited epidermolysis bullosa
Author:
Publisher
Informa UK Limited
Subject
Dermatology
Link
http://www.tandfonline.com/doi/pdf/10.1586/17469872.3.6.721
Reference71 articles.
1. Identification of mutations in a new gene encoding a FERM family protein with a pleckstrin homology domain in Kindler syndrome
2. Loss of Desmoplakin Tail Causes Lethal Acantholytic Epidermolysis Bullosa*
3. An unusual N-terminal deletion of the laminin 3a isoform leads to the chronic granulation tissue disorder laryngo-onycho-cutaneous syndrome
4. A Novel Genodermatosis Caused by Mutations in Plakophilin 1, A Structural Component of Desmosomes
5. The classification of inherited epidermolysis bullosa (EB): Report of the Third International Consensus Meeting on Diagnosis and Classification of EB
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1. Medical cell technologies for treatment of patients suffering from recessive dystrophic epidermolysis bullosa. Method of intracutaneous administration of fibroblasts;Vestnik dermatologii i venerologii;2015-06-24
2. Collagen XVII and Its Role in Junctional Epidermolysis Bullosa;Blistering Diseases;2015
3. Epidermolysis Bullosa;Emery and Rimoin's Principles and Practice of Medical Genetics;2013
4. Dystrophic Epidermolysis Bullosa: Pathogenesis and Clinical Features;Dermatologic Clinics;2010-01
5. Genetische Ursachen für epidermale Fragilität;Medizinische Genetik;2009-11-27
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