Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Michael Kruszewski"'
Autor:
Michael Lübbert, Claudia Schmoor, Tobias Berg, Michael Kruszewski, Marcus Matthias Schittenhelm, Katharina Götze, Caroline Pabst, Andrea Kündgen, Tobias Ma, Anna Frey, Kevin Moschallski, Usama-Ur Rehman, Johannes Jung, Justus Duyster, Manfred Jung, Roland Schüle, Ralph Wäsch, Olga Grishina
Publikováno v:
Blood. 140:9087-9088
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::40041dd43a77a085bf42f17e38fe27ea
https://doi.org/10.1182/blood-2022-159471
https://doi.org/10.1182/blood-2022-159471
Autor:
Jacqueline Schoumans, Sabine Blum, Michael Lübbert, Olivier Spertini, Ilaria Scarpelli, Filipe Martins, Michael Kruszewski
Publikováno v:
Annals of Hematology. 100:63-78
Myelodysplastic syndromes (MDS) are a heterogeneous group of diseases, with a variable probability of transformation into acute leukemia, which is, in the vast majority of cases, of myeloid lineage. Nevertheless, rare cases of acute lymphoblastic leu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0348cbc3b65aa234b137d3193194fd6d
https://doi.org/10.1007/s00277-020-04114-2
https://doi.org/10.1007/s00277-020-04114-2
Autor:
Filipe, Martins, Michael, Kruszewski, Ilaria, Scarpelli, Jacqueline, Schoumans, Olivier, Spertini, Michael, Lübbert, Sabine, Blum
Publikováno v:
Annals of hematology. 100(1)
Myelodysplastic syndromes (MDS) are a heterogeneous group of diseases, with a variable probability of transformation into acute leukemia, which is, in the vast majority of cases, of myeloid lineage. Nevertheless, rare cases of acute lymphoblastic leu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::139ed0e0deea1b9821c99b3099426480
https://pubmed.ncbi.nlm.nih.gov/32556451
https://pubmed.ncbi.nlm.nih.gov/32556451
Autor:
Martins, Filipe, Kruszewski, Michael, Scarpelli, Ilaria, Schoumans, Jacqueline, Spertini, Olivier, Lübbert, Michael, Blum, Sabine
Publikováno v:
Annals of Hematology; 2021, Vol. 100 Issue 1, p63-78, 16p