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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
David J Kuter,Sigbjørn Berentsen,Nichola Cooper et al. David J Kuter et al.
Autoimmune cytopenias (AICs) arise from pathogenic autoantibody-mediated destruction of blood cells. Current treatments often fail to achieve durable remission, necessitating long-term treatment including immunosuppression and exposure to t...
Yana Criel,Hendrik B Feys,Emmy De Buck et al. Yana Criel et al.
This systematic review aimed to identify clinical practice guidelines (CPGs) for platelet transfusion in non-surgical and non-traumatic care settings, and appraise their methodological quality. We searched three databases and eight grey lit...
Stavroula Parastatidou,Rozeta Sokou,Alexandra Lianou et al. Stavroula Parastatidou et al.
Congenital platelet function disorders constitute a heterogeneous group of rare, genetic conditions classified according to the affected platelet component or functionality. Sixty entities have been identified, caused by defects in around s...
José Vicente Gil,Carolina Fuentes,Miguel Ángel Verde et al. José Vicente Gil et al.
Phenocopies are leukemias that mirror the transcriptional programs, signaling dependencies and often the clinical behavior of established genetic entities, yet lack their defining lesions. In acute lymphoblastic leukemia (ALL), RNA sequenci...
Wilma Barcellini,Bruno Fattizzo Wilma Barcellini
Autoimmune hemolytic anemias comprise warm AIHA (wAIHA), due to IgG autoantibodies reacting at body temperatures, and cold agglutinin disease (CAD), due to IgM reacting in cold and strongly activating complement. The diagnosis, based on the...
Mohammadamin Noorafrooz,Ramin Noorafrooz,Giovanni Barosi et al. Mohammadamin Noorafrooz et al.
Ph-chromosome-negative myelo-proliferative neoplasms (MPNs) are characterized by over-production of mature blood cells driven by acquired somatic variants in JAK2, CALR and MPL in most instances. Ph-chromosome-negative MPNs are genetically ...
Dennis Dong Hwan Kim,Daniela Zackova,Massimo Breccia et al. Dennis Dong Hwan Kim et al.
Tyrosine kinase inhibitors have transformed survival in chronic-phase chronic myeloid leukemia, yet long-term treatment success increasingly depends on treatment tolerability. Despite its recognized influence on adherence and quality of lif...
Catherine B Ducker,Megan V Preece,Charis Pericleous et al. Catherine B Ducker et al.
The dysregulation of protective immunothrombosis is termed thrombo-inflammation. Antiphospholipid syndrome (APS) is an antibody mediated autoimmune, inflammatory and prothrombotic disease. APS is an archetypal disease for thrombo-inflammati...
Michail Makris,Paschalis Evangelidis,Nikolaos Devrikis et al. Michail Makris et al.
A disintegrin and metalloproteinase with a thrombospondin type 1 motif, member 13 (ADAMTS13), is an enzyme that cleaves ultra-large von Willebrand factor (VWF) multimers. ADAMTS13 deficiency leads to thrombotic thrombocytopenic purpura (TTP...
Malini Surapaneni,Jacob Edmisson,Attaya Suvannasankha et al. Malini Surapaneni et al.
Monoclonal gammopathy of undetermined significance (MGUS) represents a premalignant clinical state with an evolving footprint beyond its established role as a precursor to multiple myeloma. This review is intended for hematologists, oncolog...