Results 11 to 20 of about 14,443 (215)
Screening for inherited thrombophilias and prophylaxis of venous thromboembolism in pregnancy and puerperium [PDF]
Thrombophilias are a group of coagulation disorders associated with a predisposition to thrombotic events. They could be inherited (genetic) or acquired. The most encountered inherited thrombophilias are factor V Leiden (FVL), prothrombin gene mutation (
Ana SCUTELNICU +7 more
doaj +1 more source
Nephrotic syndrome (NS) is one of the most common pediatric diseases with many complications. Thromboembolic complication is the most serious complication.
Sherin Khamis Hussein +3 more
doaj +1 more source
Deficiency of protein C (PC), protein S (PS), antithrombin III (AT III), and homozygosity or combined heterozygosity for Factor V Leiden (FVL) and Factor II (FII) 20210A mutation represent severe hereditary thrombophilia (SHT) and are associated with a ...
Pasquale Madonna +4 more
doaj +1 more source
Antithrombin III: Plasma Activity and Reference Range Among Nigerian Blood Donors
Background: Diagnosis of antithrombin III (ATIII) deficiency as a common cause of thrombophilia is primarily based on the determination of antithrombin levels in plasma using a functional activity assay or an immunological assay, but local reference ...
Vincent Oluseye Osunkalu +2 more
doaj +1 more source
Quantification of antithrombin isoform proportions in plasma samples of healthy subjects, sepsis patients, and in antithrombin concentrates [PDF]
Antithrombin (AT) circulates in plasma in two isoforms, AT-alpha (90-95%) and AT-beta (5-10%). AT isoform proportions were measured in plasma samples of 17 healthy subjects and 26 posttraumatic or postoperative septic patients, as well as in 4 ...
Donges, R. +6 more
core +1 more source
Tromboembolias múltiplas associadas a défice de anti-trombina III.
Congenital deficiency of antithrombin III is considered as one serious primary hypercoagulable state. The authors present a case of deficiency of antithrombin III in a 28 years old young male, with aortic valve disease and several thromboembolic events ...
C Catarino +9 more
doaj +1 more source
A successful outcome of pregnancy in a patient with congenital antithrombin deficiency [PDF]
Background. Presence of inherited thrombophilia is an additional risk factor for maternal thromboembolism and certain adverse pregnancy outcomes, including recurrent fetal loss, placental abruption, intrauterine growth restriction and earlyonset severe ...
Kovač Mirjana +6 more
doaj +1 more source
Introduction. Recent studies have indicated an increased incidence of thrombotic vascular complications after liver transplantation. The reasons may be associated with surgical technique and “unbalanced” hemostasis in patients with diffuse liver diseases.
N. K. Kuznetsova +6 more
doaj +1 more source
Background The risk of thromboembolic events during pregnancy in patients with antithrombin deficiency is increased. Preventing thromboembolic events during pregnancy in the case of antithrombin deficiency is still a matter of concern.
Panagiotis Tsikouras +7 more
doaj +1 more source
An antibody that prevents serpin polymerisation acts by inducing a novel allosteric behavior [PDF]
Serpins are important regulators of proteolytic pathways with an antiprotease activity that involves a conformational transition from a metastable to a hyperstable state. Certain mutations permit the transition to occur in the absence of a protease; when
Faull, Sarah V. +14 more
core +1 more source

