Results 101 to 110 of about 13,148 (179)
OBJECTIVE: To analyze the preoperative plasma antigenic concentration and activity of von Willebrand factor and its main cleaving protease ADAMTS-13 in pediatric patients with cyanotic congenital heart disease undergoing surgical treatment and ...
Rosangela P.S. Soares +4 more
doaj
The essential role of calcium in ADAMTS13 function
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Gardner, Michelle Daniela +1 more
core
Atypical haemolytic-uraemic syndrome caused by factor H mutation: case report and new management strategies in children [PDF]
Atypical haemolytic uraemic syndrome is causedby alternative complement pathway dysregulation. It has recently been recognised that most cases are due to genetic factors and a growing list of mutations has been described.
Araújo, L. +5 more
core
Investigation of ADAMTS-13 levels in patients with COVID-19 infection
Introduction: Coronavirus disease 2019 (COVID-19) patients are predisposed to thrombotic events. COVID-19 coagulopathy can be associated with ADAMTS-13 (a disintegrin-like and metalloprotease with thrombospondin type I repeats 13) levels. ADAMTS-13, the
Hüseyin H Kutlu +6 more
doaj +1 more source
Background: Management of patients with refractory or frequently relapsing (r/r) immune thrombotic thrombocytopenic purpura (iTTP) remains challenging, with no established consensus on optimal therapeutic strategies.
Roman Schimmer +6 more
doaj +1 more source
A Global Assessment of Coagulation Profile and a Novel Insight into Adamts-13 Implication in Neonatal Sepsis. [PDF]
Papadogeorgou P +11 more
europepmc +1 more source
Successful Treatment of refractory Thrombotic Thrombocytopenic Purpura With The Monoclonal Antibody Rituximab :A case Report [PDF]
Much of thrombotic thrombocytopenic purpura (TTP) is attributed to the presence of an autoantibody to ADAMTS-13, the metalloprotease that degrades ultralarge von Willebrand protein multimers.
فتحی, افشین +1 more
core
A CASE OF THROMBOTIC THROMBOCYTOPENIC PURPURA RELATED TO MALIGNITY AND CHEMOTHERAPY
Objective: Thrombotic thrombocytopenic purpura (TTP) is a life-threatening multisystem disease. TTP progresses with Microangiopathic hemolytic anemia (MAHA), fever, thrombocytopenia, neurological symptoms, and renal failure.
Ebru Kavak Yavuz +5 more
doaj +1 more source
Targeting the von Willebrand Factor-ADAMTS-13 axis in sickle cell disease. [PDF]
Ellsworth P, Sparkenbaugh EM.
europepmc +1 more source
Assay for ADAMTS-13 Activity with Flow Cytometric Readout. [PDF]
Müller J +5 more
europepmc +1 more source

