Behçet's Disease (Adamantiades-Behçet's Disease)
Adamantiades-Behçet's disease (ABD) is characterized by starting with oral aphthous ulceration and developing of the systemic involvements. The pathogenesis of ABD is closely correlated with the genetic factors and the triggering factors which acquire delayed-type hypersensitivity reaction agai...
Saved in:
Main Authors: | Fumio Kaneko, Ari Togashi, Sanae Saito, Hideo Sakuma, Noritaka Oyama, Koichiro Nakamura, Kenji Yokota, Keiji Oguma |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2011-01-01
|
Series: | Clinical and Developmental Immunology |
Online Access: | http://dx.doi.org/10.1155/2011/681956 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Hyperhomocysteinaemia in Behçet's Disease
by: Amira Hamzaoui, et al.
Published: (2010-01-01) -
Update on the Medical Management of Gastrointestinal Behçet’s Disease
by: Giuseppe Lopalco, et al.
Published: (2017-01-01) -
Gender Differences in Behçet’s Disease Associated Uveitis
by: Didar Ucar-Comlekoglu, et al.
Published: (2014-01-01) -
Mean Platelet Volume in Ocular Behçet’s Disease
by: Fatih Mehmet Türkcü, et al.
Published: (2013-01-01) -
MicroRNA Expression Profiling in Behçet’s Disease
by: Antonio Puccetti, et al.
Published: (2018-01-01)