Association of severe rheumatoid arthritis with heterozygosity for α-antitrypsin deficiency
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1980.tb00125.x/fullpdf
Reference28 articles.
1. Increased frequency of the MZ phenotype of alpha-1-protease inhibitor in juvenile chronic polyarthritis;Arnaud;J. clin. Invest.,1977
2. Proteinase inhibitors in rheumatoid arthritis;Brackertz;Ann. rheum. Dis.,1975
3. Criteria for juvenile rheumatoid arthritis;Brewer;Bull. Rheum. Dis.,1973
4. α1-Antitrypsin phenotypes in rheumatoid arthritis and ankylosing spondylitis;Buisseret;Lancet,1977
5. The effect of D-penicillamine on polymorphonuclear leukocyte function;Chuslinska-Sadowska;J. clin. Invest.,1976
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1. Application of Salivary Alpha-1 Antitrypsin in the Diagnosis of Rheumatoid Arthritis: A Pilot Study;Medicina;2024-04-06
2. Point Mutation of a Non-Elastase-Binding Site in Human α1-Antitrypsin Alters Its Anti-Inflammatory Properties;Frontiers in Immunology;2018-05-01
3. Identification of carbamylated alpha 1 anti-trypsin (A1AT) as an antigenic target of anti-CarP antibodies in patients with rheumatoid arthritis;Journal of Autoimmunity;2017-06
4. Other Diseases Associated With Alpha-1 Antitrypsin Deficiency;Blanco's Overview of Alpha-1 Antitrypsin Deficiency;2017
5. Alpha-1 Antitrypsin: A Potent Anti-Inflammatory and Potential Novel Therapeutic Agent;Archivum Immunologiae et Therapiae Experimentalis;2012-02-15
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