Zobrazeno 1 - 10
of 337
pro vyhledávání: '"D A Tsakiris"'
Autor:
D. A. Tsakiris, G. Stussi
Publikováno v:
Hämostaseologie. 32:63-66
SummaryAllogeneic and autologous hematopoietic stem cell transplantations are important therapeutic options for patients with hematologic disorders. Hemostatic complications are frequent after hematopoietic stem cell transplantation with a considerab
Publikováno v:
DMW - Deutsche Medizinische Wochenschrift. 120:1109-1113
Statement of problem To analyse whether lipoprotein(a) is a risk factor for myocardial infarction, stroke and acute peripheral arterial occlusion in coronary heart disease and whether this risk can be assessed by clotting activation markers. Patients
Publikováno v:
Blood Coagulation & Fibrinolysis. 11:165-173
Autor:
L, Graf, D A, Tsakiris
Publikováno v:
Praxis. 101(7)
Heritable thrombophilia as a concept in hemostasis has been continuously discovered parallel to the knowledge on physiology of bleeding disorders. Since the 1980s it has become increasingly popular to search for thrombophilia in patients with thrombo
Autor:
L M, Asmis, L, Alberio, A, Angelillo-Scherrer, W, Korte, A, Mendez, G, Reber, B, Seifert, H, Stricker, D A, Tsakiris, W A, Wuillemin
Publikováno v:
Thrombosis research. 129(4)
Rivaroxaban (RXA) is licensed for prophylaxis of venous thromboembolism after major orthopaedic surgery of the lower limbs. Currently, no test to quantify RXA in plasma has been validated in an inter-laboratory setting. Our study had three aims: to a
Publikováno v:
Der Internist. 52(1)
Anesthesiologists and surgeons are increasingly faced with patients who are under long-term medication. Some of these drugs can interact with anaesthetics or anaesthesia and/or surgical interventions. As a result, patients may experience complication
Publikováno v:
Der Anaesthesist. 60(5)
Thrombotic microangiopathies are characterized by platelet activation, endothelial damage, hemolysis and microvascular occlusion. This group of diseases is primary represented by thrombotic thrombocytopenic purpura (TTP) and hemolytic uremic syndrome
Autor:
B, Zieger, A, Jenny, D A, Tsakiris, I, Bartsch, K, Sandrock, C, Schubart, S, Schäfer, An, Busse, Walter A, Wuillemin
Publikováno v:
Hamostaseologie. 29(2)
Bernard-Soulier syndrome (BSS) is a rare, autosomal recessive inherited bleeding disorder associated with thrombocytopenia, thrombocytopathy and giant platelets. BSS is caused by genetic alterations of the glycoprotein (GP) Ib/V/IX complex. We report
Publikováno v:
Allergy. 61(12)
Anticoagulants, including heparins, coumarins, hirudins, and some of the previously used plasma volume expanders, belong to the most widely used drugs. Hypersensitivity reactions from these agents are uncommon. However, they may have a considerable i
Publikováno v:
Allergy. 61(6)