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Blood|November 8, 2012
Allogeneic hematopoietic cell transplantation for XIAP deficiency: an international survey reveals poor outcomesRebecca A Marsh, Kanchan Rao, Prakash Satwani, et al.Blood Advances|January 20, 2026
Comparable outcomes of HSCT upfront and after failure of IST in pediatric aplastic anemia in recent yearsFelicia Andresen, Ayami Yoshimi, Peter Bader, et al.Leukemia|September 13, 2022
Incidence of subsequent malignancies after total body irradiation-based allogeneic HSCT in children with ALL - long-term follow-up from the prospective ALL-SCT 2003 trialAnna Eichinger, Ulrike Poetschger, Evgenia Glogova, et al.Blood|April 22, 2016
The minimum required level of donor chimerism in hereditary hemophagocytic lymphohistiocytosisBernd Hartz, Rebecca Marsh, Kanchan Rao, et al.The Journal of Allergy and Clinical Immunology|September 28, 2025
Late effects after hematopoietic stem cell transplantation in patients with HLH: A Histiocyte Society, PDWP, IEWP, and TCWP EBMT StudyKim Ramme, AnnaCarin Horne, Karin Beutel, et al.Bone Marrow Transplantation|July 10, 2021
Hematopoietic stem cell transplantation in children and adolescents with GATA2-related myelodysplastic syndromeRachel Bortnick, Marcin Wlodarski, Valerie de Haas, et al.Leukemia|November 27, 2019
Correction: Hematopoietic stem cell transplantation for children with acute myeloid leukemia-results of the AML SCT-BFM 2007 trialMartin G Sauer, Peter J Lang, Michael H Albert, et al.Bone Marrow Transplantation|May 16, 2019
Presence of centromeric but absence of telomeric group B KIR haplotypes in stem cell donors improve leukaemia control after HSCT for childhood ALLFlorian Babor, Christina Peters, Angela R Manser, et al.Leukemia|October 4, 2019
Hematopoietic stem cell transplantation for children with acute myeloid leukemia-results of the AML SCT-BFM 2007 trialMartin G Sauer, Peter J Lang, Michael H Albert, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 10, 2026
European expert recommendations for comprehensive pre-treatment, treatment-phase and post-treatment care of patients with metachromatic leukodystrophy treated with autologous haematopoietic stem and progenitor cell gene therapyLucia Laugwitz, Francesca Fumagalli, Katharina Wehner, et al.Pageof 13