Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Roswith Eisert"'
Publikováno v:
Klinische Pädiatrie. 224:211-226
To learn more about prioritisation in the health care system, we performed an exploratory qualitative study on haemophilia A. The aim was to generate haemophilia disease-specific criteria and to learn more about reasoning in the decision-making proce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7544ec84d7ab1a497e275abc1e99905a
https://doi.org/10.1055/s-0032-1306302
https://doi.org/10.1055/s-0032-1306302
Publikováno v:
Sozialer Fortschritt. 60:73-81
Die aktuelle Debatte um Rationierung oder Priorisierung medizinischer Leistungen beruhrt die Frage nach dem Solidarprinzip der GKV und dem Solidaritatsverstandnis ihrer Versicherten. Der vorliegende Beitrag stellt Ergebnisse einer empirischen Untersu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ad800294ac7dedcdb2f7b71e81b5893a
https://doi.org/10.3790/sfo.60.4-5.73
https://doi.org/10.3790/sfo.60.4-5.73
Autor:
Jürgen Horst, Hartmut Pollmann, Roswith Eisert, Albena Todorova, Marcin Chlystun, Nadja Bogdanova, C. Wermes, Arseni Markoff, Ulrike Nowak-Göttl
Publikováno v:
Human Mutation. 28:54-60
The amount of residual F8 (FVIII:C) determines the clinical severity of hemophilia A. Recently, we showed that the mutation detection rate in severely affected male patients (FVIII:C1% of normal) is virtually 100% when testing for the common intron 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d86d1684f365ff5db86e351d3eeb3e49
https://doi.org/10.1002/humu.20403
https://doi.org/10.1002/humu.20403
Autor:
Arseni Markoff, Ulrike Nowak-Göttl, Jürgen Horst, Albena Todorova, Nadja Bogdanova, Bernd Dworniczak, C. Wermes, Hartmut Pollmann, Antonin Eigel, Roswith Eisert
Publikováno v:
Human Mutation. 26:249-254
Hemophilia A is the most frequently occurring X-linked bleeding disorder, affecting one to two out of 10,000 males worldwide. Various types of mutations in the F8 gene are causative for this condition. It is well known that the most common mutation i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56d67baf5119908e3f3df07c90b5ed98
https://doi.org/10.1002/humu.20208
https://doi.org/10.1002/humu.20208
Autor:
Arnold Ganser, Silke Ehrenforth, Inge Scharrer, Mario von Depka, Roswith Eisert, Andreas Czwalinna, C. Wermes
Publikováno v:
Thrombosis and Haemostasis. 89:847-852
SummaryACE displays potent vasoconstrictive effects, attenuation of fibrinolysis, and platelet activation and aggregation, thus possibly promoting venous thromboembolism (VTE). The ACE gene contains an insertion (I) or deletion (D) polymorphism accou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::026e0532e029c36ef83ecfe519c87349
https://doi.org/10.1055/s-0037-1613472
https://doi.org/10.1055/s-0037-1613472
Autor:
Arnold Ganser, Ulrike Nowak-Göttl, Monika Barthels, Inge Scharrer, Roswith Eisert, Silke Ehrenforth, Christian Dieterich, Mario von Depka
Publikováno v:
Blood. 96:3364-3368
Elevation of serum lipoprotein (a) (Lp[a]) is a known risk factor predisposing to cardiovascular and cerebrovascular disease. However, little is known about the role of increased Lp(a) in venous thromboembolism (VTE). This study evaluated the role of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58a136d7c23eb4c85ba49b748b368843
https://doi.org/10.1182/blood.v96.10.3364
https://doi.org/10.1182/blood.v96.10.3364
Autor:
Roswith Eisert, Christiane De Rop, Arnold Ganser, Arne Trummer, Stefanie Buchholz, Michael B. Stadler
Publikováno v:
Transplantation. 92(3)
Background There is compelling evidence that blood-borne tissue factor that is predominantly found on circulating microparticles (MPs) plays an important role in both, cancer biology and organ and stem-cell transplantation (SCT). Therefore, we hypoth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6049c05a9e8e942ca45c5d262160b47b
https://pubmed.ncbi.nlm.nih.gov/21730890
https://pubmed.ncbi.nlm.nih.gov/21730890
Publikováno v:
Das Gesundheitswesen. 71
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1acb6c4bc0d1405d0c1340b82b8898d3
https://doi.org/10.1055/s-0029-1239113
https://doi.org/10.1055/s-0029-1239113
Autor:
Nadja, Bogdanova, Arseni, Markoff, Hartmut, Pollmann, Ulrike, Nowak-Göttl, Roswith, Eisert, Bernd, Dworniczak, Antonin, Eigel, Jürgen, Horst
Publikováno v:
Human mutation. 20(3)
Hemophilia A is a common X-linked bleeding disorder caused by various types of mutations in the factor VIII gene F8C. The most common intron 22-inversion is responsible for about 40% of the severe hemophilia A cases while large deletions, point mutat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8fc93221be97a043b8398f7825950d1b
https://pubmed.ncbi.nlm.nih.gov/12204009
https://pubmed.ncbi.nlm.nih.gov/12204009
Autor:
Silke Ehrenforth, Arnold Ganser, Inge Scharrer, Cornelia Wermes, Roswith Eisert, Andreas Czwalinna, Mario von Depka
Publikováno v:
Thrombosis and haemostasis. 86(6)
Summary Background: The endothelial cell protein C receptor (EPCR) enhances protein C activation by the thrombin-thrombomodulin complex. As evidence is accumulating that EPCR is an important component of the protein C anticoagulant pathway, polymorph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92a1a097640d3a5714b8661faf1fd978
https://pubmed.ncbi.nlm.nih.gov/11776299
https://pubmed.ncbi.nlm.nih.gov/11776299