Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Hein Hustinx"'
Autor:
Eva-Maria Dauber, Wolfgang R. Mayr, Hein Hustinx, Marlies Schönbacher, Holger Budde, Tobias J. Legler, Margit König, Oskar A. Haas, Gerhard Fritsch, Günther F. Körmöczi
Publikováno v:
Haematologica, Vol 104, Iss 3 (2019)
Spontaneous Rh blood group changes are a striking sign, reported to occur mainly in patients with hematologic disorders. Upon routine blood grouping, 2 unrelated individuals showed unexplained mixed red cell phenotype regarding the highly immunogenic
Externí odkaz:
https://doaj.org/article/ccccaaf4d2074f94bdea0560698999c6
Publikováno v:
Transfusion. 60:2399-2407
ALX148, a novel CD47 blocking agent, is in clinical development for the treatment of advanced solid tumors and lymphoma. Because CD47 is highly expressed on red blood cells (RBCs), its therapeutic blockade can potentially interfere with pretransfusio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c63a0a228ef5a7cd2443398bf700f718
https://doi.org/10.1111/trf.16009
https://doi.org/10.1111/trf.16009
Autor:
Margit König, Hein Hustinx, Tobias J. Legler, Holger Budde, Wolfgang R. Mayr, Gerhard Fritsch, Oskar A. Haas, Marlies Schönbacher, E.M. Dauber, Günther F. Körmöczi
Publikováno v:
Haematologica
Spontaneous Rh blood group changes are a striking sign, reported to occur mainly in patients with hematologic disorders. Upon routine blood grouping, 2 unrelated individuals showed unexplained mixed red cell phenotype regarding the highly immunogenic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::356e28270cbda79f28232029cf85a319
http://europepmc.org/articles/PMC6395338
http://europepmc.org/articles/PMC6395338
Autor:
Laura Infanti, Adrian Bachofner, Sofia Lejon Crottet, Andreas Buser, Hein Hustinx, Tanja Rüfli, Andreas Holbro, Matyas Escedi
Herein we describe a case of febrile non-hemolytic reaction (FNHTR) in a 64-year-old male 20 min after the transfusion of one red blood cell unit. 20 days prior the patient had undergone an allogeneic hematopoietic stem cell transplantation (HCT) fro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8681ec0716db7239c7a97deef4be3e9b
https://www.zora.uzh.ch/id/eprint/184585/
https://www.zora.uzh.ch/id/eprint/184585/
Autor:
Hein Hustinx, Sonja Sigurdardottir, Andreas Maier, Judith Ries, Amira Sarraj, Christoph Gassner, Andreas Buser, Alexander Markovic, Emmanuel Rigal, Stefan Meyer, Damiano Castelli, Claudia Portmann, Nadine Trost, Beat M. Frey, Monica C. Braisch, Bettina Weingand, Laura Infanti, Caren Vollmert, Jutta Thierbach, Jochen Gottschalk, Simon M. Mauvais, Soraya Amar el Dusouqui
Publikováno v:
British Journal of Haematology. 174:624-636
Results of genotyping with true high-throughput capability for MNSs antigens are underrepresented, probably because of technical issues, due to the high level of nucleotide sequence homology of the paralogous genes GYPA, GYPB and GYPE. Eight MNSs-spe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c85a0bcc223db10ee1fa93153212d7ea
https://doi.org/10.1111/bjh.14095
https://doi.org/10.1111/bjh.14095
Autor:
Christoph Gassner, Beat M. Frey, Sofia Lejon Crottet, Behrouz Mansouri Taleghani, Christoph Niederhauser, Jochen Gottschalk, Stefano Fontana, Hein Hustinx, Christine Henny, Stefan Meyer, Peter Gowland, Kathrin Neuenschwander, Franziska Still, Martin Stolz
Publikováno v:
Transfusion and Apheresis Science. 50:169-174
Starting in 2013, blood donors must be tested at least using: (1) one monoclonal anti-D and one anti-CDE (alternatively full RhCcEe phenotyping), and (2) all RhD negative donors must be tested for RHD exons 5 and 10 plus one further exonic, or intron
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::880a197a8f253a40f768fb9519ceff8a
https://doi.org/10.1016/j.transci.2014.02.011
https://doi.org/10.1016/j.transci.2014.02.011
Autor:
Romina Kardashi, Manuela Schulz, Fuping Liu, Louise Y. C. Takeshita, Abdulgabar Salama, Wolfgang Helmberg, Olga Arbach, Franz F. Wagner, Hein Hustinx, Ziyi He, Santosh Kumar Patnaik, Gottfried Fischer, Josef Evers, Olga O. Blumenfeld, Volker Braun, Andrew R. Jones, Willy A. Flegel, Beat M. Frey, Maria-Inti Metzendorf, Derek Middleton, Cynthia Flickinger, Faviel F. Gonzalez-Galarza
Publikováno v:
Transfusion Medicine and Hemotherapy. 41:333-337
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bd6e1571a4825c9dfb5e80674fed2ea9
https://doi.org/10.1159/000368868
https://doi.org/10.1159/000368868
Publikováno v:
Immunohematology. 32(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4a08c9d5a4c234774635cfaf3549e400
https://pubmed.ncbi.nlm.nih.gov/27901571
https://pubmed.ncbi.nlm.nih.gov/27901571
Autor:
Nirmeen A. Fayed, Dominik Franz, Joachim Oertel, Wessam Mourad, Sven Martens, Heiko Müller, Hermann Eichler, Hans H. Scheld, Oliver M. Theusinger, Isabelle Müller, Philipp Stein, Laura Infanti, Christian Juhra, Andreas Buser, Michael J. Raschke, Matthias Borowski, Dania Fischer, Cora Alexandra Vökt, Hein Hustinx, Robert Kwiecien, Jerrold H. Levy, Patrick Meybohm, Khaled Yassen, Thomas Braschler, Klaus Görlinger, Heinrich Rotering, Clemens Kösters, Donat R. Spahn, Matthias Lange, Hubert Buddendick, Raoul Georg Geissler, Norbert Roeder, Christof Geisen, Kai Zacharowski, Markus Müller, Cornelia M. Keck, Dorothee Hartmann, Walter Sibrowski, Peter Schlenke, Andreas Holbro, Holger Bunzemeier, Erhard Seifried, Gabriela H. Spahn, Thierry Peyrard
Publikováno v:
Transfusion Medicine and Hemotherapy. 42:69-71
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2dc7063e8d0d1c591c0a7d331f04405d
https://doi.org/10.1159/000382104
https://doi.org/10.1159/000382104
Autor:
René Jørgensen, Åsa Hellberg, Hein Hustinx, Mark H. Yazer, Martin L. Olsson, Monica M. Palcic, Thierry Peyrard, Annika K. Hult
Publikováno v:
Transfusion. 50:1471-1486
BACKGROUND: The 1061delC single-nucleotide polymorphism (SNP) has been reported mostly in the context of the common A(2)[A201] allele and typically produces an A(2) phenotype. This study evaluated new A(weak) alleles, each containing 1061delC. STUDY
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9621f1e1a0fc3d2e50734e7eb359750c
https://doi.org/10.1111/j.1537-2995.2010.02670.x
https://doi.org/10.1111/j.1537-2995.2010.02670.x