Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Christian M Schambeck"'
Autor:
Karl Winkler, Vera Krane, Dialysis Study Investigators, Mario Berger, Christoph Wanner, Christian M. Schambeck, Jürgen Lilienthal
Publikováno v:
Clinical Journal of the American Society of Nephrology. 5:874-881
Background and objectives: Hemodialysis patients with type 2 diabetes exhibit an excessive cardiovascular risk and regularly receive heparin. We tested whether antibodies to the platelet factor 4–heparin complex (PF4-H-AB) contribute to outcome. De
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::afa8132d5dd0e21e6c3878a6182d8ec4
https://doi.org/10.2215/cjn.01170209
https://doi.org/10.2215/cjn.01170209
Autor:
Florian Thieme, Christian M. Schambeck
Publikováno v:
Der Klinikarzt. 38:432-436
Molecular biological methods for thrombophilia screening have found their way into the coagulation laboratory since the middle of the eighties. Beside the frequent factor-V-Leiden-mutation and the prothrombin-G20210A-polymorphism a number of mutation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::18a10d82998e4eb927c180fb6887bbba
https://doi.org/10.1055/s-0029-1243263
https://doi.org/10.1055/s-0029-1243263
Autor:
Christian M. Schambeck
Publikováno v:
LaboratoriumsMedizin. 32:397-400
ZusammenfassungVon einer familiären Häufung von Lupusantikoagulanz und Anticardiolipin-Antikörper wurde immer wieder berichtet. Der Nachweis von Antiphospholipid-Antikörpern innerhalb einer Familie war nur gelegentlich mit klinischen Ereignissen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9d89e8a64a7386cb6a9ae74278815714
https://doi.org/10.1515/jlm.2008.065
https://doi.org/10.1515/jlm.2008.065
Autor:
Christian M Schambeck, Gerd Schmitz
Publikováno v:
Pathophysiology of Haemostasis and Thrombosis. 35:166-174
Platelet function is sensitive to alterations in cholesterol metabolism, and hypercholesterolemia is associated with enhanced platelet reagibility. Atherogenic low-density lipoproteins (LDL), in particular oxidized LDL, activate src-kinase-family-dep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d52fb6aaf4bdbc8abe25607c90b21c54
https://doi.org/10.1159/000093563
https://doi.org/10.1159/000093563
Autor:
Christian M. Schambeck
Publikováno v:
LaboratoriumsMedizin. 28:453-462
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::500c46d33b11d32863568f0f10236db1
https://doi.org/10.1515/labmed.2004.061
https://doi.org/10.1515/labmed.2004.061
Autor:
Kathleen Teuchert, Alois Spahn, Mario Berger, Christian M. Schambeck, Ralf Grossmann, Ulrich Walter, Sarah Zonnur
Publikováno v:
Thrombosis and Haemostasis. 92:42-46
SummaryTheoretically, von Willebrand factor (VWF) should be capable of binding all factor VIII (FVIII), but an unbound FVIII (uFVIII) plasma fraction remains. In patients’ status post deep-vein thrombosis (DVT), an altered uFVIII fraction and high
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4adee9cb815df7e9c363acdb6947c621
https://doi.org/10.1160/th04-02-0063
https://doi.org/10.1160/th04-02-0063
Autor:
Franz Keller, B. Mansouri Taleghani, Christian M. Schambeck, D. Wahler, I. Haubitz, K. Hinney
Publikováno v:
Arteriosclerosis, Thrombosis, and Vascular Biology. 21:289-292
Abstract —High levels of factor VIII (FVIII) but not von Willebrand factor (vWF) are known to increase the risk for venous thromboembolism. Whether high FVIII levels originate from hereditary defects or from acquired conditions remains unanswered.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9b74a20bcfed05b0007116dd19fe538
https://doi.org/10.1161/01.atv.21.2.289
https://doi.org/10.1161/01.atv.21.2.289
Autor:
Christian M. Schambeck, Petra Zeitler, Francoise Meire, Stefan Seregard, Anne-Marie Mingers, Hans Wolfgang Kreth, Ugur Ozcelik, Deniz Anadol, Volker Schuster, Lori Luchtman-Jones
Publikováno v:
Scopus-Elsevier
SummarySevere type I plasminogen deficiency has been recently linked to ligneous conjunctivitis, a rare and uncommon form of chronic conjunctivitis. In this study, eight unrelated ligneous conjunctivitis patients living in different parts of the worl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4bc43a38855fc5fd644c783f5be013cb
https://doi.org/10.1055/s-0037-1615955
https://doi.org/10.1055/s-0037-1615955
Publikováno v:
Thrombosis and Haemostasis. 85:782-786
SummaryHypercoagulability is observed in patients with inherited thrombophilia, e.g. factor V Leiden (FVL) mutation. Pregnancy represents a hypercoagulable state as well. This study addresses the effects of the FVL mutation on haemostatic activation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b954611f519812cbce8fb72ca33ab484
https://doi.org/10.1055/s-0037-1615718
https://doi.org/10.1055/s-0037-1615718
Publikováno v:
Thrombosis and Haemostasis. 78:1480-1483
SummaryThe cumulative thrombotic risk of Factor V (FV) Leiden and oral contraceptives (OC) recommends screening for the mutation. Assuming that a family history of thrombosis increases the patient’s likelihood of bearing FV Leiden, a selective rath
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aaedb942685a33801c403344537683a3
https://doi.org/10.1055/s-0038-1665437
https://doi.org/10.1055/s-0038-1665437