Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Heike, Berghöfer"'
Autor:
Sentot Santoso, Behnaz Bayat, Silke Werth, Annalena Traum, Jieging Zhu, Heike Berghöfer, Gregor Bein, Ulrich J. Sachs
Publikováno v:
Thromb Haemost
Background Fetal/neonatal alloimmune thrombocytopenia (FNAIT) results from maternal alloantibodies (abs) reacting with fetal platelets expressing paternal human platelet antigens (HPAs), mostly HPA-1a. Anti-HPA-1a abs, are the most frequent cause of
Autor:
Silke Schmidt, Sentot Santoso, Lars Fischer, Roongaroon Phuangtham, Sarah Theresa Holzwarth, Jieqing Zhu, Doris Boeckelmann, Lida Röder, Behnaz Bayat, Gregor Bein, Heike Berghöfer
Publikováno v:
Transfusion
Background Fetal and neonatal alloimmune thrombocytopenia (FNAIT) is caused by the destruction of platelets in the fetus or newborn by maternal platelet alloantibodies, mostly against human platelet antigen (HPA)-1a. Recent studies indicate that two
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af29212f5c5160d87d0c4def68e1df01
https://europepmc.org/articles/PMC8020566/
https://europepmc.org/articles/PMC8020566/
Autor:
Sentot Santoso, Lida Röder, Ulrich J. Sachs, Gregor Bein, Heike Berghöfer, Kathrin Heidinger, Hevi Wihadmadyatami
Publikováno v:
Thrombosis and Haemostasis. 116:262-271
SummaryTreatment of bleeding in patients with Glanzmann’s thrombasthenia (GT) can be hampered by iso-antibodies against the αIIbβ3 integrin, which cause rapid clearance of transfused donor platelets. Type 1 GT patients with a total absence of αI
Autor:
Ulrich J. Sachs, Silke Werth, Gregor Bein, Yudy Tjahjono, John Eskandar, Sentot Santoso, Behnaz Bayat, Heike Berghöfer
Publikováno v:
Transfusion. 53:193-201
BACKGROUND: Several methods exist for the detection of neutrophil antibodies; most of them, however, require fresh neutrophils. In this study, an enzyme-linked immunosorbent assay (ELISA) using recombinant HNA-1 antigens (rHNAs) was developed to dete
Autor:
Heike Berghöfer, Sentot Santoso, Jürgen Bux, Behnaz Bayat, Wiebke Wasel, Ulrich J. Sachs, Gregor Bein, Angelika Reil, Katja Hattar, Norbert Weissmann, Rainer M. Bohle
Publikováno v:
Blood. 117:669-677
Transfusion-related acute lung injury (TRALI) is the leading cause of transfusion-associated mortality in the United States and other countries. In most TRALI cases, human leukocyte antigen (HLA) class II antibodies are detected in implicated donors.
Autor:
Heike Berghöfer, Hartmut Kroll, Ulrich J. Sachs, Axel Matzdorff, Sentot Santoso, José A. López
Publikováno v:
British Journal of Haematology. 123:127-131
Summary. Bernard–Soulier syndrome (BSS) is a rare inherited disorder with giant platelets, thrombocytopenia and a prolonged bleeding time. These abnormalities are caused by genetic defects of the glycoprotein (GP) Ib-IX complex that constitutes the
Autor:
Silke, Werth, Behnaz, Bayat, Yudy, Tjahjono, John, Eskandar, Heike, Berghöfer, Gregor, Bein, Ulrich J, Sachs, Sentot, Santoso
Publikováno v:
Transfusion. 53(1)
Several methods exist for the detection of neutrophil antibodies; most of them, however, require fresh neutrophils. In this study, an enzyme-linked immunosorbent assay (ELISA) using recombinant HNA-1 antigens (rHNAs) was developed to detect HNA-1a, -
Autor:
Behnaz, Bayat, Yudy, Tjahjono, Silke, Werth, Heike, Berghöfer, Angelika, Reil, Hartmut, Kroll, Ulrich J, Sachs, Sentot, Santoso
Publikováno v:
Transfusion. 52(3)
Alloantibodies against human neutrophil antigen-3 (HNA-3) are responsible for the fatalities reported in transfusion-related acute lung injury. Consequently, reliable detection of these alloantibodies is mandatory to improve blood transfusion safety.
Autor:
Ulrich J H, Sachs, Hartmut, Kroll, Axel C, Matzdorff, Heike, Berghöfer, José A, Löpez, Sentot, Santoso
Publikováno v:
British journal of haematology. 123(1)
Bernard-Soulier syndrome (BSS) is a rare inherited disorder with giant platelets, thrombocytopenia and a prolonged bleeding time. These abnormalities are caused by genetic defects of the glycoprotein (GP) Ib-IX complex that constitutes the von Willeb