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Study Reveals Stigma Patterns in Sickle Cell Disease
April 2026
New research shows sickle cell disease bias in clinician notes is more closely associated with opioid use than race or chronic pain, highlighting documentation disparities.
Read more
26 Mar 2026
EBMT 2026: Machine Learning Predicts Graft Failure After Transplant
A machine learning approach reveals structural HLA biomarkers linked to graft failure, offering a new strategy for donor selection in transplantation.
25 Mar 2026
EBMT 2026: Memory T Cell Therapy Boosts Post-transplant Immunity
CD45RA depleted memory T cell therapy shows encouraging results in treating infections after transplant, with high survival and viral clearance rates in early findings.
25 Mar 2026
EBMT 2026: Gene Therapy Adoption Gaps in Sickle Cell Care
Survey data reveal strong support for gene therapy in sickle cell disease, but inconsistent referral practices, limited knowledge, and insurance barriers hinder implementation.
24 Mar 2026
Liquid Biopsy Accelerates Diagnosis of Burkitt’s Lymphoma
Liquid biopsy significantly reduced the median turnaround time from 46.8 days to just 6.5 days, offering a substantial improvement in diagnostic efficiency.
21 Mar 2026
Study Proves Favourable Safety of Apixaban Over Rivaroxaban
Castellucci and colleagues identified that a primary-outcome event had occurred in 44 (3.3%) of the 1,345 patients taking apixaban, compared to 96 (7.1%) of the 1,355 in the rivaroxaban group.
17 Mar 2026
Brain and Spinal Cord Relapse Risk Identified in Leukaemia
A large retrospective study identified risk factors for CNS relapse after transplant in adults with acute lymphoblastic leukaemia, highlighting elevated risk in Philadelphia chromosome positive disease.
15 Mar 2026
Ribosome Biogenesis Target Identified in Acute Myeloid Leukaemia
A study identifies the ribosome biogenesis factor MYBBP1A as essential for acute myeloid leukaemia cell growth, revealing a potential therapeutic vulnerability.
15 Mar 2026
Epigenetic Silencing Challenges AAV Gene Therapy Durability
Analysis of patient liver biopsies and cell models suggests epigenetic silencing may limit durability of AAV gene therapy, offering insight into long term variability in haemophilia treatment.
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