IgG4-related Systemic Disease in a Native American Man
Author:
Affiliation:
1. Department of Medicine, Mayo Clinic, USA
Publisher
Japanese Society of Internal Medicine
Subject
General Medicine,Internal Medicine
Link
http://www.jstage.jst.go.jp/article/internalmedicine/50/8/50_8_931/_pdf
Reference24 articles.
1. Hyper-IgG4 disease: report and characterisation of a new disease
2. 2. Chari ST. Diagnosis of autoimmune pancreatitis using its five cardinal features: introducing the Mayo Clinic's HISORt criteria. J Gastroenterol 42 Suppl 18: 39-41, 2007.
3. Proposal for a new clinical entity, IgG4-positive multiorgan lymphoproliferative syndrome: analysis of 64 cases of IgG4-related disorders
4. IgG4-related sclerosing disease
5. IgG4-associated Multifocal Systemic Fibrosis Complicating Sclerosing Sialadenitis, Hypophysitis, and Retroperitoneal Fibrosis, but Lacking Pancreatic Involvement
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