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期刊名:Blood reviews

缩写:BLOOD REV

ISSN:0268-960X

e-ISSN:1532-1681

IF/分区:7.2/Q1

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共收录本刊相关文章索引892
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Xenia Bubnova,Lauren Hope,Helen Wheadon Xenia Bubnova
Leukaemia is caused by genetic mutations within haematopoietic stem and progenitor cells, leading to the production of immature blasts. While mouse models have been instrumental in studying disease mechanisms and testing therapies, their li...
Alex Wonnaparhown,Talal Hilal,Albert Chong et al. Alex Wonnaparhown et al.
The treatment of lymphoid malignancies is rapidly advancing with recognition of hypogammaglobulinemia (HG) and increased infection risk with the use of cellular-targeted therapies, such as chimeric antigen receptor (CAR) T cell and bispecif...
Baher Krayem,Avraham Frisch,Netanel Horowitz Baher Krayem
The prognosis of patients with AML varies significantly with age, driven by biological heterogeneity and age-associated factors such as comorbidities, functional status, and hospitalization burden. Many novel therapies have been approved in...
Alain Mina,Yazan Madanat,Yasmin Abaza et al. Alain Mina et al.
Myelodysplastic syndromes/neoplasms (MDS) are a group of clonal myeloid malignancies characterized by ineffective hematopoiesis, cytopenias, and an increased risk of transformation to acute myeloid leukemia (AML). In lower-risk (LR) MDS, as...
Sophie Roux,Françoise Debiais,Marie-Hélène Vieillard Sophie Roux
Bone involvement in multiple myeloma (MM) is marked by osteolysis, driven by excessive bone resorption and a profound suppression of bone formation. Interactions between MM cells and the bone microenvironment-mediated by integrins,chemokine...
Yesim Dargaud,Sebastien Lobet,Nathalie Roussel et al. Yesim Dargaud et al.
Hemophilia A and B are rare X-linked bleeding disorders caused by coagulation factor deficiencies, leading to joint bleeding, synovial hypertrophy and chronic hemophilic arthropathy marked by progressive cartilage and bone damage. Musculosk...
Tobias Dittrich,Lina Weinert,Anita D&#x;Souza Tobias Dittrich
Systemic light chain (AL) amyloidosis often results in multi-organ dysfunction and significant morbidity. Clinical assessments may not capture the full impact of disease and treatment on patients. Patient-reported outcomes (PROs) can help f...
Shuang Liu,Yan Shen,Jiayi Chen et al. Shuang Liu et al.
Venous thromboembolism (VTE), encompassing deep vein thrombosis (DVT) and pulmonary embolism (PE), is a complex vascular disorder with high morbidity and mortality, driven by Virchow's Triad: blood stasis, hypercoagulability, and endothelia...
Anam Ashfaque,Yara Shatnawi,Shahzad Raza et al. Anam Ashfaque et al.
Light chain (AL amyloidosis) is a rare disorder characterized by the deposition of misfolded light chains in various organs, causing progressive organ damage. Current therapeutic agents do not remove amyloid aggregates already present in th...
Tomás José González-López,Drew Provan Tomás José González-López
The purpose of this review is to highlight the treatments currently available and those under- going evaluation in clinical trials for the treatment of ITP in order to achieve optimal use of the various existing ITP treatments. Specifically...