Clinical relevance of feto-maternal microchimerism in (hematopoietic stem cell) transplantation. [PDF]
Kruchen A, Fehse B, Müller I.
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Globally, sickle cell disease (SCD) is the most common inherited haemoglobinopathy. The highest burden of SCD is encountered in low‐ and middle‐income countries (LMICs), most of which lack the resources to contend with the disease. Blood transfusion remains central to the emergent treatment and prevention of complications of SCD.
Jeremy W. Jacobs+13 more
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Cell Therapy as a Way to Increase the Effectiveness of Hematopoietic Stem Cell Transplantation. [PDF]
Pashkina E+4 more
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Plerixafor alone for the mobilization and transplantation of HLA-matched sibling donor hematopoietic stem cells [PDF]
Chen, Yi-Bin, DiPersio, John F., et al,
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Myeloid neoplasm inspired intensive therapy in VEXAS syndrome: A single‐centre experience
Summary There is still no standard of care and unmet medical needs in refractory/advanced VEXAS (vacuoles in myeloid progenitors, E1 ubiquitin activating enzyme, X‐linked, autoinflammatory manifestations and somatic) syndrome with or without associated haematological neoplasm.
Maël Heiblig+5 more
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The Progress of Autologous Hematopoietic Stem Cell Transplantation in the Treatment of Multiple Myeloma (Review). [PDF]
Wang YN, Zhang CW, Gao YX, Ge XL.
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Myeloablative autologous stem-cell transplantation for severe scleroderma [PDF]
Brasington, R., et al,
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In our central morphological review system, megakaryocyte counts are prioritized alongside BM cellularity to differentiate between AA and MDS. A retrospective analysis of patients with SAA and those with LR‐hMDS, registered in that system, revealed a significant difference in outcomes.
Tomoya Maeda+25 more
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Case study: Acute plasmoblastic leukemia presentation following effective haploidentical hematopoietic stem cell transplantation therapy. [PDF]
Karabekov A+7 more
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Adult T‐cell leukaemia/lymphoma (ATLL) is a rare, aggressive cancer linked to HTLV‐1, with poor outcomes. We analysed 79 ATLL patients (1993–2023) at our institution. The median age at diagnosis was 47 years, with 72% of patients of Caribbean origin. Median progression‐free and overall survival were 10.2 and 16.2 months respectively. CNS involvement at
Tomohiro Aoki+11 more
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