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Meta-analysis of the clinical and immunopathological characteristics and treatment outcomes in epidermolysis bullosa acquisita patients

BACKGROUND: Epidermolysis bullosa acquisita (EBA) is an orphan autoimmune disease. Several clinical phenotypes have been described, but subepidermal blistering is characteristic of all variants. Limited data on clinical and immunopathological characteristics and treatment outcomes in EBA are availab...

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Detaylı Bibliyografya
Yayımlandı:Orphanet J Rare Dis
Asıl Yazarlar: Iwata, Hiroaki, Vorobyev, Artem, Koga, Hiroshi, Recke, Andreas, Zillikens, Detlef, Prost-Squarcioni, Catherine, Ishii, Norito, Hashimoto, Takashi, Ludwig, Ralf J.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2018
Konular:
Research
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6122731/
https://ncbi.nlm.nih.gov/pubmed/30180870
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-018-0896-1
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