Results 81 to 90 of about 38,829 (239)
Anetoderma: Is It a Sign of Autoimmunity?
Anetoderma is a rare elastolytic disorder characterized by circumscribed areas of flaccid skin due to the loss of elastic tissue in the dermis. Primary anetoderma is frequently observed in patients with autoimmune diseases or abnormalities especially ...
Hessa Al Buainain, Mohamed Allam
doaj +1 more source
Prevalence, significance and predictive value of antiphospholipid antibodies in Crohn’s disease [PDF]
AIM: To assess the prevalence and stability of different antiphospholipid antibodies (APLAs) and their association with disease phenotype and progression in inflammatory bowel diseases (IBD) patients.
Altorjay, István +11 more
core +1 more source
Advancing Extracellular Vesicle Research: A Review of Systems Biology and Multiomics Perspectives
ABSTRACT Extracellular vesicles (EVs) are membrane‐bound vesicles secreted by various cell types into the extracellular space and play a role in intercellular communication. Their molecular cargo varies depending on the cell of origin and its functional state.
Gloria Kemunto +2 more
wiley +1 more source
Background To identify the mechanisms of the hypercoagulability associated with antiphospholipid antibodies, we investigated antibody-mediated platelet activation and interference of antibodies with phospholipid-dependent reactions.Design and Methods We ...
Aurelie Membre +6 more
doaj +1 more source
Case of severe hypertension and nephrotic range proteinuria [PDF]
No abstract ...
Bursztyn, Michael +4 more
core +1 more source
Objectives: The study was designed to an estimate the prevalence of antiphospholipid IgG and IgM antibodies with toxoplasmosis patients among aborted and non-aborted women. Methodology: A total number of 70 Iraqi patients aborted and non-aborted women
Alaa hashim Abd-Ali Al-Maliki
doaj +1 more source
Antiphospholipid Antibody Syndrome
Antiphospholipid antibodies are directed against phospholipid-protein complexes and include lupus anticoagulant, anticardiolipin antibodies, and anti–beta-2 glycoprotein I antibodies. Antiphospholipid antibody syndrome is a common cause of acquired thrombophilia and is characterized by venous or arterial thromboembolism or pregnancy morbidity and the ...
Nikhil A, Sangle, Kristi J, Smock
openaire +2 more sources
Classification of Platelet‐Activating Anti‐Platelet Factor 4 Disorders
ABSTRACT Introduction The prototypic anti‐platelet factor 4 (PF4) disorder—heparin‐induced thrombocytopenia and thrombosis (HITT)—features immunoglobulin G (IgG) class antibodies that activate platelets, monocytes, and neutrophils in a mainly heparin‐dependent fashion via Fcγ receptor‐dependent cellular activation.
Theodore E. Warkentin
wiley +1 more source
Association of anticardiolipin, antiphosphatidylserine, anti-β2 glycoprotein I, and antiphosphatidylcholine autoantibodies with canine immune thrombocytopenia [PDF]
β2GPI expression and identification.
Chau-Loong Tsang +12 more
core +4 more sources

