Thrombotic thrombocytopenic purpura: pathophysiology, diagnosis, and management
S Sukumar, B Lämmle, SR Cataland - Journal of clinical medicine, 2021 - mdpi.com
Thrombotic thrombocytopenic purpura (TTP) is a rare thrombotic microangiopathy
characterized by microangiopathic hemolytic anemia, severe thrombocytopenia, and …
characterized by microangiopathic hemolytic anemia, severe thrombocytopenia, and …
Guidelines on the use of therapeutic apheresis in clinical practice–evidence‐based approach from the writing committee of the American society for apheresis: the …
J Schwartz, A Padmanabhan, N Aqui… - Journal of clinical …, 2016 - Wiley Online Library
The American Society for Apheresis (ASFA) Journal of Clinical Apheresis (JCA) Special
Issue Writing Committee is charged with reviewing, updating, and categorizing indications …
Issue Writing Committee is charged with reviewing, updating, and categorizing indications …
Mechanisms of autoantibody-induced pathology
RJ Ludwig, K Vanhoorelbeke, F Leypoldt… - Frontiers in …, 2017 - frontiersin.org
Autoantibodies are frequently observed in healthy individuals. In a minority of these
individuals, they lead to manifestation of autoimmune diseases, such as rheumatoid arthritis …
individuals, they lead to manifestation of autoimmune diseases, such as rheumatoid arthritis …
Thrombotic thrombocytopenic purpura
JA Kremer Hovinga, P Coppo, B Lämmle… - Nature reviews Disease …, 2017 - nature.com
Thrombotic thrombocytopenic purpura (TTP; also known as Moschcowitz disease) is
characterized by the concomitant occurrence of often severe thrombocytopenia …
characterized by the concomitant occurrence of often severe thrombocytopenia …
Recombinant ADAMTS-13: first-in-human pharmacokinetics and safety in congenital thrombotic thrombocytopenic purpura
Safety, tolerability, and pharmacokinetics of recombinant ADAMTS-13 (a disintegrin and
metalloproteinase with a thrombospondin type 1 motif, member 13; BAX 930; SHP655) were …
metalloproteinase with a thrombospondin type 1 motif, member 13; BAX 930; SHP655) were …
IgG4-related disease
JH Stone, Y Zen, V Deshpande - New England Journal of …, 2012 - Mass Medical Soc
IgG4-Related Disease | New England Journal of Medicine Skip to main content The New
England Journal of Medicine homepage Advanced Search SEARCH SPECIALTIES Cardiology …
England Journal of Medicine homepage Advanced Search SEARCH SPECIALTIES Cardiology …
Guidelines on the use of therapeutic apheresis in clinical practice—evidence‐based approach from the Writing Committee of the American Society for Apheresis: the …
The American Society for Apheresis (ASFA) JCA Special Issue Writing Committee is
charged with reviewing, updating and categorizating indications for therapeutic apheresis …
charged with reviewing, updating and categorizating indications for therapeutic apheresis …
Guidelines on the use of therapeutic apheresis in clinical practice—evidence‐based approach from the Apheresis Applications Committee of the American Society for …
ZM Szczepiorkowski, JL Winters… - Journal of clinical …, 2010 - Wiley Online Library
Abstract The American Society for Apheresis (ASFA) Apheresis Applications Committee is
charged with a review and categorization of indications for therapeutic apheresis. Beginning …
charged with a review and categorization of indications for therapeutic apheresis. Beginning …
Immunology of IgG4-related disease
E Della-Torre, M Lanzillotta… - Clinical & Experimental …, 2015 - academic.oup.com
Immunoglobulin G4-related disease (IgG4-RD) is a fibroinflammatory condition that derives
its name from the characteristic finding of abundant IgG4+ plasma cells in affected tissues …
its name from the characteristic finding of abundant IgG4+ plasma cells in affected tissues …
Natural history of Upshaw–Schulman syndrome based on ADAMTS13 gene analysis in Japan
Y Fujimura, M Matsumoto, A Isonishi… - … of Thrombosis and …, 2011 - Wiley Online Library
Upshaw–Schulman syndrome (USS) is an extremely rare hereditary deficiency of
ADAMTS13 activity, termed congenital TTP. The clinical signs are usually mild during …
ADAMTS13 activity, termed congenital TTP. The clinical signs are usually mild during …