Zobrazeno 1 - 10
of 56
pro vyhledávání: '"Juergen Foell"'
Autor:
Amadeus T Heinz, Friso G.J. Calkoen, Alexander Derbich, Lea Miltner, Christian Seitz, Michaela Doering, Christiane Braun, Daniel Atar, Michael Schumm, Florian Heubach, Anne-Marie Arendt, Ansgar Schulz, Friedhelm R Schuster, Roland Meisel, Brigitte Strahm, Juergen Finke, Beatrice Heineking, Susanne Stetter, Gerda Silling, Daniel Stachel, Bernd Gruhn, Klaus-Michael Debatin, Juergen Foell, Johannes H Schulte, Wilhelm Woessmann, Christine Mauz-Körholz, Johanna Tischer, Tobias Feuchtinger, Rupert Handgretinger, Peter Lang
Publikováno v:
Haematologica, Vol 108, Iss 8 (2023)
Therapy-resistant viral reactivations contribute significantly to mortality after hematopoietic stem cell transplantation. Adoptive cellular therapy with virus-specific T cells (VST) has shown efficacy in various single-center trials. However, the sc
Externí odkaz:
https://doaj.org/article/6ada467cb16540358957b223184585b6
Publikováno v:
Hematology/Oncology and Stem Cell Therapy, Vol 13, Iss 2, Pp 98-105 (2020)
Sickle cell disease (SCD) is an inherited disorder; despite significant improvements in supportive care, SCD continues to cause substantial morbidity, mortality, and reduced life expectancy. Allogeneic hematopoietic stem cell transplantation (HSCT) i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d708d048107270925b0ba0f9a9b407ec
http://www.sciencedirect.com/science/article/pii/S1658387620300248
http://www.sciencedirect.com/science/article/pii/S1658387620300248
Autor:
Angela Yen, Damiano Rondelli, la Fuente Josu de, Amanda M. Li, Jennifer Domm, Montalembert Mariane de, Tony W. Ho, Donna A. Wall, Brenda K. Eustace, Juergen Foell, Sujit Sheth, Haydar Frangoul, Rupert Handgretinger, Akshay Sharma, Sandeep Soni, Antonis Kattamis, Andrew Kernytsky, Franco Locatelli, Stephan A. Grupp, M. Domenica Cappellini, Julie A. Lekstrom-Himes, Selim Corbacioglu, David Altshuler, Markus Y. Mapara, Yi-Shan Chen, Martin H. Steinberg
Transfusion-dependent β-thalassemia (TDT) and sickle cell disease (SCD) are severe monogenic diseases with severe and potentially life-threatening manifestations. BCL11A is a transcription factor that represses γ-globin expression and fetal hemoglo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::294f2984b8848005c8f160412c9178cd
https://hdl.handle.net/10807/228473
https://hdl.handle.net/10807/228473
Bone marrow aspirations in oncological patients: experience from an in-house standard in paediatrics
Publikováno v:
Wiener Medizinische Wochenschrift. 169:82-86
Nearly all paediatric patients require deep sedation when undergoing bone marrow aspiration (BMA). We analyzed the data from our protocols documented in a standardised procedure for bone marrow puncture over a period of 2 years. Our standard included
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::759dc5ae3b161722941f8bc128735bba
https://doi.org/10.1007/s10354-017-0611-1
https://doi.org/10.1007/s10354-017-0611-1
Autor:
Matthias Edinger, Johannes H. Schulte, Peter Lang, Anja Troeger, Daniel Wolff, Charalampos Aslanidis, Ernst Holler, Selim Corbacioglu, Petra Hofmann, Juergen Foell, Angelika Eggert, Beatrix Pfirstinger
Publikováno v:
Bone marrow transplantation. 54(11)
Despite significant improvements in the supportive care, sickle cell disease (SCD) leads to significant morbidity and mortality. Allogeneic hematopoietic stem cell transplantation (HSCT), the only curative option, is limited due to matched donor avai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::053ef1748cfc4091033ffb29008f13d7
https://pubmed.ncbi.nlm.nih.gov/31089288
https://pubmed.ncbi.nlm.nih.gov/31089288
Autor:
Mohrez, Morad1, Troeger, Anja2, Kleinschmidt, Katharina2, Alali, Tarek Hanafee2, Jakob, Marcus2, Brosig, Andreas1, Hähnel, Viola1, Kietz, Silke2, Offner, Robert1, Burkhardt, Ralph1, Corbacioglu, Selim2, Ahrens, Norbert1, Foell, Juergen2 juergen.foell@ukr.de
Publikováno v:
European Journal of Haematology. Nov2023, Vol. 111 Issue 5, p824-830. 7p.
Publikováno v:
Bone Marrow Transplantation. 52:938-940
Haploidentical stem cell transplantation with CD3 + -/CD19 + - depleted peripheral stem cells for patients with advanced stage sickle cell disease and no alternative donor: results of a pilot study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a286746701ae43266fb3aec86f9450c0
https://doi.org/10.1038/bmt.2017.49
https://doi.org/10.1038/bmt.2017.49
Autor:
Anja Troeger, Beatrix Pfirstinger, Morad Morez, Norbert Ahrens, Selim Corbacioglu, Ralph Burkhardt, Andreas Brosig, Juergen Foell, Katharina Kleinschmidt
Publikováno v:
Blood. 134:1171-1171
Introduction Allogeneic haematopoietic stem cell transplantation (HSCT) is currently the only curative treatment for sickle cell disease (SCD) offered to patients with a fully matched sibling (MSD) or matched unrelated donor (MUD). With a MSD/MUD don
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::984e6c9209295714f33d7d210f103cd1
https://doi.org/10.1182/blood-2019-131984
https://doi.org/10.1182/blood-2019-131984
Autor:
Beatrix Pfirstinger, Katharina Kleinschmidt, Charalampos Aslanidis, Wolfgang Herr, Angelika Eggert, Juergen Foell, Anja Troeger, Selim Corbacioglu, Matthias Edinger, Daniel Wolff, Johannes H. Schulte, Ernst Holler
Publikováno v:
Blood. 132:2088-2088
Introduction: Sickle cell disease (SCD) is one of the most prevalent monogenic hematological disorders leading to progressive multi-organ damage and reduced life expectancy despite a significant improvement of conventional and supportive care. Alloge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5fd1242d15b310096f5d4522dcffed08
https://doi.org/10.1182/blood-2018-99-115988
https://doi.org/10.1182/blood-2018-99-115988
Autor:
Juergen Foell, Matthias Edinger, Daniel Wolff, Ernst Holler, Angelika Eggert, Wolfgang Herr, Charalampos Aslanidis, Selim Corbacioglu, Petra Hoffmann, Beatrix Pfirstinger, Anja Troeger, Johannes H. Schulte
Publikováno v:
Blood. 132:3455-3455
Background: Sickle cell disease (SCD) is an inherited disorder with an estimate of 300,000 affected newborns per year worldwide. Despite improvements in preventive measures and conventional therapy, substantial morbidity and mortality, resulting in a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a0ae3e1496c6d865836f69a438aa075
https://doi.org/10.1182/blood-2018-99-114695
https://doi.org/10.1182/blood-2018-99-114695