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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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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
Najmaldin Saki,Hakimeh Hadi,Bijan Keikhaei et al. Najmaldin Saki et al.
Immune thrombocytopenia (ITP) is an autoimmune bleeding disorder characterized by excessive reticuloendothelial platelet destruction and inadequate compensatory platelet production. However, the pathogenesis of ITP is relatively complex, an...
Clifton C Mo,Edward Richardson,Eleonora Calabretta et al. Clifton C Mo et al.
Patients with multiple myeloma (MM) were among the groups impacted more severely by the COVID-19 pandemic, with higher rates of severe disease and COVID-19-related mortality. MM and COVID-19, plus post-acute sequelae of SARS-CoV-2 infection...
Jorune Balciuniene,Yi Ning,Hillard M Lazarus et al. Jorune Balciuniene et al.
Since the discovery of the Philadelphia chromosome in 1960, cytogenetic studies have been instrumental in detecting chromosomal abnormalities that can inform cancer diagnosis, treatment, and risk assessment efforts. The initial expansion of...
Bo Xu,Bo Kang,Jixiang Chen et al. Bo Xu et al.
Paroxysmal nocturnal hemoglobinuria (PNH) is a rare, clonal, complement-mediated hemolytic anemia with a variety of manifestations. Currently, the methods for treating PNH include anti-C5 treatments (eculizumab and ravulizumab) and pegcetac...
Madelyn Burkart,Shira Dinner Madelyn Burkart
There have been major paradigm shifts in the treatment of Philadelphia chromosome negative (Ph-) acute lymphoblastic leukemia (ALL) in the last decade with the introduction of new immunotherapies and targeted agents, adoption of pediatric-t...
Jinghua Wang,Jian Li,Liye Zhong Jinghua Wang
Amyloid light-chain (AL) amyloidosis is a rare hematological disease that produces abnormal monoclonal immunoglobulin light chains to form amyloid fibrils that are deposited in tissues, resulting in organ damage and dysfunction. Advanced AL...
Morgana Pinheiro Maux Lessa,Alexandre Soares Ferreira Junior,Margaret Graton et al. Morgana Pinheiro Maux Lessa et al.
When de-novo immune-mediated thrombotic thrombocytopenic purpura (TTP) is diagnosed following an invasive procedure, clinical presentation patterns and outcomes are poorly defined. Therefore, in a systematic literature review of patients di...
Yun Wang,Zhi-Jian Liang,Robert Peter Gale et al. Yun Wang et al.
Chronic myeloid leukaemia (CML) is caused by BCR::ABL1. Tyrosine kinase-inhibitors (TKIs) are the initial therapy. Several organizations have reported milestones to evaluate response to initial TKI-therapy and suggest when a change of TKI s...
Paul Telfer,Kofi A Anie,Stella Kotsiopoulou et al. Paul Telfer et al.
The acute pain crisis (APC) is the commonest complication of sickle cell disease (SCD). Severe episodes may require treatment in hospital with strong opioid analgesic drugs, combined with additional supportive care measures. Guidelines for ...
Dominic J Fowler-Shorten,Charlotte Hellmich,Matthew Markham et al. Dominic J Fowler-Shorten et al.
B-cell lymphoma-2 (BCL-2) family proteins are fundamental regulators of the intrinsic apoptotic pathway which modulate cellular fate. In many haematological malignancies, overexpression of anti-apoptotic factors (BCL-2, BCL-XL and MCL-1) ci...