Results 21 to 30 of about 225,640 (263)
Impaired thrombin generation as a reproducible feature of bleeding disorder of unknown cause
Background: Thrombin generation (TG) has previously been investigated in patients with bleeding disorder of unknown cause (BDUC) with discrepant results.
Tim Dreier +6 more
doaj +1 more source
Changes in Blood Viscosity With Synthetic Protease Inhibitors
We examined the effects on whole blood viscosity and coagulation time of various dosages of the synthetic low-molecular protease inhibitors gabexate mesilate and nafamostat mesilate with an oscillation-type viscometer.
Masahito Hitosugi +6 more
doaj +1 more source
In blood coagulation, circulating platelets and coagulation factors are crucial for the primary process because thrombi are generated by fibrin clotting with fibrinogen, thrombin, FXIIIa, and platelet activation.
Jun-Hui Choi, Seung Kim
doaj +1 more source
Background Aggressive fluid management and other external factors may lead to hypothermia, acidosis and hemodilution (defined as Lethal Triad, LT) contributing to a trauma-induced coagulopathy (TIC) that worsens patients’ outcomes.
Julia K. Böhm +5 more
doaj +1 more source
THE REGULATORY ROLE OF COAGULATION FACTORS ON ARTERIAL FUNCTION
The coagulation takes place in the physiological system of hemostasis. Hemostasis is known to be disturbed in many diseases leading to hemorrhages or thrombosis.
Jeremy Lagrange
doaj +1 more source
Responses of some blood coagulation factors in recovery period after interval and continuous efforts for swimmers [PDF]
تحددت مشكلة البحث في دراسة استجابات بعض عوامل تخثر الدم في فترة استعادة الشفاء بعد الجهدين الفتري والمستمر لدى السباحين. وهدف البحث إلى الكشف عن استجابات بعض عوامل تخثر الدم في فترة الاستشفاء بعد الجهد الفتري والمستمر وفي فترة الاستشفاء(1) ساعة بعد ...
Nashwan I. Abdullah
doaj +1 more source
Blood coagulation factor VIII: An overview
Factor VIII (FVIII) functions as a co-factor in the blood coagulation cascade for the proteolytic activation of factor X by factor IXa. Deficiency of FVIII causes hemophilia A, the most commonly inherited bleeding disorder. This review highlights current knowledge on selected aspects of FVIII in which both the scientist and the clinician should be ...
G M, Bhopale, R K, Nanda
openaire +2 more sources
Introduction The thrombin generation (TG) test is a global hemostasis assay sensitive to procoagulant conditions. However, some TG assays may underestimate elevated TG when the thrombin fluorogenic substrate is depleted or fluorescence is attenuated by ...
William C. Chang +4 more
doaj +1 more source
ABSTRACT Background Therapeutic apheresis (TA) is an established treatment modality for hematologic, neurologic, and immunologic disorders, yet access remains severely limited in sub‐Saharan Africa. Donor apheresis, including platelet apheresis collection from healthy donors, represents an important complementary modality supporting blood product ...
Nosa Bazuaye +33 more
wiley +1 more source
Management of a Patient with Bombay Blood Group and Chronic Liver Disease with Subdural Hematoma
The Bombay blood group is an extremely rare entity within the conventional ABO blood grouping system. End-stage liver disease also presents with myriad disorders of coagulation due to impaired synthesis and dysfunction of clotting factors, which ...
Siddharth Chavali +3 more
doaj +1 more source

