The classification of inherited epidermolysis bullosa (EB): Report of the Third International Consensus Meeting on Diagnosis and Classification of EB.
By J. Fine, R. Eady, E. Bauer, J. Bauer, L. Bruckner-Tuderman, A. Heagerty, H. Hintner, A. Hovnanian, M. Jonkman, I. Leigh and 8 more. Journal of American Academy of Dermatology, 2008
900 citations recorded by the source corpus.
Subfields: Cell Biology, Genetics, Physiology
View Paper: https://www.semanticscholar.org/paper/ed5b919b6c91564623be5a01aa5be7469603511e
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
- J. Fine
- L. Bruckner-Tuderman
- P. Elias
- C. Has
- R. Eady
- V. Oji
- Eugene A. Bauer
- J. W. Bauer
Citations in the corpus
- Inherited epidermolysis bullosa: updated recommendations on diagnosis and classification. (2014, methodology): “When the classification system was last revised, EBS was further separated into suprabasal and basal subgroups, based on the histopathologic site of cleavage within the epidermis.(1) In the past EBS was referred to by some as ‘‘epidermolytic’’ although this term is inaccurate, because cellular lysis”
- Extracellular Matrix Reorganization During Wound Healing and Its Impact on Abnormal Scarring (2015, neutral): “A subset of the skin blistering diseases, epidermolysis bullosa is caused by a collagen VII gene defect.(18) See Table 1 for a more complete listing of human skin diseases associated with collagen mutations.”
- Revised nomenclature and classification of inherited ichthyoses: results of the First Ichthyosis Consensus Conference in Sorèze 2009. (2010, background): “Hystrix skin changes can be observed in other ichthyoses, eg, KID syndrome (Table XII), or in particular types of ectodermal dysplasia.69 The annular EI (Fig 3, E ), which is a result of KRT1 or KRT10 mutations,70,71 is classified as a clinical variant of EI.”