Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Eva Boog-Whiteside"'
Autor:
Jekaterina Malina, Eva-Maria Huessler, Karl-Heinz Jöckel, Eva Boog-Whiteside, Nicole Jeschonneck, Bernadette Schröder, Rebecca Schüle, Tobias Kühl, Stephan Klebe
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-14 (2024)
Abstract Background Hereditary spastic paraplegia (HSP) is a rare neurodegenerative disease that lacks specific and validated patient-centered outcome measures (PCOMs). We aimed to develop and validate a health-related quality of life (HRQoL) questio
Externí odkaz:
https://doaj.org/article/4624ec559bc4406a87707f259b4728b7
Autor:
Meike Farber, Yiyang Chen, Lucas Arnold, Michael Möllmann, Eva Boog-Whiteside, Yu-An Lin, H. Christian Reinhardt, Ulrich Dührsen, Maher Hanoun
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-11 (2021)
Abstract Targeting the interaction between leukemic cells and the microenvironment is an appealing approach to enhance the therapeutic efficacy in acute myeloid leukemia (AML). AML infiltration induces a significant release of inflammatory cytokines
Externí odkaz:
https://doaj.org/article/d97d5af41fbb4c26838feff8bdc564fe
Autor:
Yiyang Chen, Maher Hanoun, Ulrich Dührsen, Yu-An Lin, H. Christian Reinhardt, Eva Boog-Whiteside, Lucas Arnold, Meike Farber, Michael Möllmann
Publikováno v:
Scientific Reports
Scientific Reports, Vol 11, Iss 1, Pp 1-11 (2021)
Scientific Reports, Vol 11, Iss 1, Pp 1-11 (2021)
Targeting the interaction between leukemic cells and the microenvironment is an appealing approach to enhance the therapeutic efficacy in acute myeloid leukemia (AML). AML infiltration induces a significant release of inflammatory cytokines in the hu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f12ec2ec6e105b6e22b718f406ea8784
http://europepmc.org/articles/PMC8586007
http://europepmc.org/articles/PMC8586007
Autor:
Malina, Jekaterina1 (AUTHOR), Huessler, Eva-Maria2 (AUTHOR), Jöckel, Karl-Heinz2 (AUTHOR), Boog-Whiteside, Eva1 (AUTHOR), Jeschonneck, Nicole1 (AUTHOR), Schröder, Bernadette3 (AUTHOR), Schüle, Rebecca4,5,6 (AUTHOR), Kühl, Tobias3 (AUTHOR), Klebe, Stephan1 (AUTHOR) stephan.klebe@uk-essen.de
Publikováno v:
Orphanet Journal of Rare Diseases. 1/2/2024, Vol. 19 Issue 1, p1-14. 14p.