Thrombotic thrombocytopenic purpura in IgG4-related disease with severe deficiency of ADAMTS-13 activity and IgG4 autoantibody against ADAMTS-13-Reference-Cited by-同舟云学术

Thrombotic thrombocytopenic purpura in IgG4-related disease with severe deficiency of ADAMTS-13 activity and IgG4 autoantibody against ADAMTS-13

Published:2011-08 Issue:8 Volume:63 Page:1209-1212
ISSN:2151-464X
Container-title:Arthritis Care & Research
language:en
Short-container-title:Arthritis Care Res

Author:

Saeki Takako,Ito Tomoyuki,Youkou Akira,Ishiguro Hajime,Sato Naoko,Yamazaki Hajime,Koike Tadashi,Kourakata Hiroyo,Ferrari Silvia,Scheiflinger Friedrich,Narita Ichiei

Publisher

Wiley

Subject

Rheumatology

Reference14 articles.

1. Proposal for a new clinical entity, IgG4-positive multi-organ lymphoproliferative syndrome: analysis of 64 cases of IgG4-related disorders;Masaki;Ann Rheum Dis,2009

2. High serum IgG4 concentrations in patients with sclerosing pancreatitis;Hamano;N Engl J Med,2001

4. Clinicopathological characteristics of patients with IgG4-related tubulointerstitial nephritis;Saeki;Kidney Int,2010

5. A case of autoimmune pancreatitis complicated with immune thrombocytopenia during maintenance therapy with prednisolone;Nakamura;Dig Dis Sci,2003

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