Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Ruediger E. Scharf"'
Publikováno v:
Perfusion. 26:334-340
Rotation thromboelastography (ROTEM) is a screening method that allows the rapid detection of plasma- and platelet-related haemostatic abnormalities. To use this procedure more efficiently, reference values depending on gender, age, and oral contrace
Autor:
Michael Sabel, Ruediger E. Scharf, Rainer B. Zotz, Christoph Sucker, Walter Stummer, Andrea Gerhardt
Publikováno v:
Clinical and Applied Thrombosis/Hemostasis. 14:472-475
The authors report on the first successful use of recombinant activated factor VII for the prophylaxis of bleeding during brain tumor neurosurgery in a patient suffering from inherited factor XI deficiency. Using the agent, surgery was performed with
Autor:
Winfried März, Bernhard O. Boehm, Rainer B. Zotz, C. Müller, Ruediger E. Scharf, Bernhard R. Winkelmann
Publikováno v:
Journal of Thrombosis and Haemostasis. 3:1522-1529
Summary. Conflicting results of an association of the human platelet antigen 1b (HPA-1b/PlA2), localized on the β-subunit of the integrin αIIbβ3, and the α2807TT genotype of the integrin α2β1 with coronary atherosclerosis and myocardial infarct
Publikováno v:
Haemophilia. 15:377-379
Autor:
Rainer B. Zotz, Christoph Sucker, Joachim Cyran, Ali Ghodsizad, Ruediger E. Scharf, Norbert Scheffold
Publikováno v:
International Journal of Cardiology. 123:355-357
Polymorphisms of receptors involved in platelet adhesion and aggregation modulate platelet thrombogenicity and were found to predispose to premature arterial thromboses in individuals at risk. In our current study, we assessed the potential relevance
Publikováno v:
Journal of thrombosis and thrombolysis. 37(2)
The risk of premature manifestation of cardiovascular disease is higher in women after a maternal placental syndrome, especially with a history of fetal IUGR. Aim of the study was to assess hereditary risk factors for arterial thrombosis as risk fact
Autor:
Boris Fehse, Olga Shardakova, Guenther Giers, Kristoffer Weber, Volker R. Stoldt, Marcus Stockschlaeder, Ruediger E. Scharf
Publikováno v:
Blood coagulationfibrinolysis : an international journal in haemostasis and thrombosis. 21(5)
Postnatal vasculogenesis has been implicated as an important mechanism for neovascularization via bone marrow-derived endothelial progenitor cells (EPCs) circulating in peripheral blood. In preparation of the utilization of EPCs in clinical protocols
Autor:
Bernd Grabensee, Christine Kurschat, Ruediger E. Scharf, Ljerka Ostojic, Rainer B. Zotz, Gerd R. Hetzel, Robert Loncar, Christoph Sucker, Beate Maruhn-Debowski
Publikováno v:
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis. 15(3)
Factor V Leiden (FVL) mutation and prothrombin G20210A mutation are common hereditary risk factors for venous thrombosis. In the current study, 40 patients (mean age ± standard deviation, 35 ± 11 years) and 764 healthy control subjects (mean age ±
Auch in der 2. Auflage begleitet Sie die'Hämostaseologie für die Praxis'sicher durch den klinischen Alltag. Aktualisierte Beiträge und neue Kapitel im Grundlagen- und Methodenteil gewährleisten den'State of the Art'dieses fundierten Werks. Bewäh
Autor:
Gerd Ruediger Hetzel, Beate Maruhn-Debowski, Rainer B. Zotz, Christoph Sucker, Bernd Grabensee, Fieras Dahhan, Christine Kurschat, Firuseh Farokhzad, Ruediger E. Scharf, Michael Schmitz
Publikováno v:
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association. 22(5)
Background. Thrombotic microangiopathies are characterized by microvascular thrombosis, consequently leading to microangiopathic haemolytic anaemia, thrombocytopenia and organ dysfunction. Although recent research has elucidated the pathogenesis of t