Results 121 to 130 of about 13,808 (210)
Clinical practice guidelines for the management of atypical haemolytic uraemic syndrome in the United Kingdom [PDF]
, +4 more
core +1 more source
Mesenchymal stem cells (MSCs) are known to facilitate angiogenesis and promote neo-vascularization via secretion of trophic factors. Here, we explored the molecular mechanism adopted by ADAMTS13 in modulating the expression of some key angiogenic markers
Srishti Dutta Gupta, Malancha Ta
doaj +1 more source
The role of complement in Streptococcus pneumoniae-associated haemolytic uraemic syndrome [PDF]
Background. Atypical forms of haemolytic uraemic syndrome (aHUS) include HUS caused by defects in the regulation of alternative complement pathway and HUS linked to neuraminidase- producing pathogens, such as Streptococcus pneumoniae. Increasing data
Szilágyi, Ágnes
core
Thrombotic thrombocytopenic purpura (TTP) is a life-threatening thrombotic microangiopathic (TMA) disorder characterized by severe thrombocytopenia, haemolytic anemia and severe organ failure. The pathophysiology of TTP is linked to a deficiency in the haemostatic multi-domain protease ADAMTS13 (A Disintegrin And Metalloprotease domain with ...
openaire +2 more sources
ADAMTS13 deficiency with elevated levels of ultra-large and active von Willebrand factor in P. falciparum and P. vivax malaria. [PDF]
A deficiency in ADAMTS13 (a von Willebrand factor [VWF] cleaving protease) is associated with accumulation of prothrombogenic unusually large VWF multimers (UL-VWF) in plasma. We studied VWF release and proteolysis in patients with symptomatic Plasmodium
Syafruddin D
core
ADAMTS13 ameliorates diabetic nephropathy by Nrf2/GPX4/eNOS signaling pathway. [PDF]
Wang H +13 more
europepmc +1 more source
Thrombotic microangiopathy overlap syndrome in pregnancy. [PDF]
Han J +4 more
europepmc +1 more source

