IGF2BP3 Promoted the Over-Proliferation of AML Cells via Stability NRXN2 mRNA [0.03%]
IGF2BP3通过稳定NRXN2mRNA促进急性髓系白血病细胞过度增殖
Wenyue Ma,Letian Sun,Siling Liu et al.
Wenyue Ma et al.
Objective: Acute myeloid leukemia (AML) is a malignant tumor with high incidence and mortality. This study aimed to investigate whether insulin-like growth factor 2 mRNA binding protein 3 (IGF2BP3) regulates the stability...
Salvage Treatment Options for Post-Transplant Relapse in Children with Early/Very Early Relapse of Acute Lymphoblastic Leukemia: A Single Center Experience [0.03%]
儿童早期复发急性淋巴细胞白血病异基因造血干细胞移植后复发的挽救治疗：单中心经验
Zühre Kaya,Serap Kirkiz Kayalı,Ahmet Bayramlı et al.
Zühre Kaya et al.
This study aimed to evaluate salvage treatment options for posttransplant relapse in children with early/very early relapse acute lymphoblastic leukemia (ALL). Forty consecutive high-risk ALL children were divided into two groups based on t...
A Large Room for Improvement Concerning the Management of Relapsed Refractory Large B-cell Lymphoma in Türkiye: Real-World Outcomes in the Setting Without Access to T-Cell Redirecting Therapies [0.03%]
土耳其针对复发/难治性弥漫大B细胞淋巴瘤的管理存在较大改进空间：在缺乏T细胞重定向疗法的情况下，真实世界的结果不容乐观
Umut Yılmaz,Mehmet Sinan Dal,Turgay Ulaş et al.
Umut Yılmaz et al.
Objectives: Large B-cell lymphoma (LBCL) patients who fail frontline therapy (R/R-LBCL) experience highly unfavorable outcomes. The development of T-cell redirecting therapies is rapidly evolving this outlook. However, co...
Spontaneous Hematotympanium in a Chronic Lymphocytic Leukemia Patient Receiving Ibrutinib: A Rare Bleeding Complication [0.03%]
伊布替尼治疗慢性淋巴细胞白血病患者自发性耳腔出血1例报告
Serkan Ünal,Murat Yaşar,Güven Yılmaz
Serkan Ünal
Beyond the Usual Suspects: Unexplained Childhood Hemolytic Anemia with Myopathy Unveiling as Glycogen Storage Disease Type XII [0.03%]
不出所料的 suspects：一种以溶血性贫血和肌病为表现的糖原贮积症十二型
Amiya Ranjan Nayak,Tribikram Panda,Meghana P et al.
Amiya Ranjan Nayak et al.
All-Cause and Exacerbation-Related Readmissions in Thrombotic Microangiopathy Requiring Plasmapheresis: A Population-Based Cohort Study [0.03%]
血栓性微血管病的全因和加重相关再住院：人群队列研究
Alexander R Thebert,Toru Yoshino,Sae X Morita et al.
Alexander R Thebert et al.
Objective: Thrombotic microangiopathy (TMA) is a serious condition characterized by microangiopathic hemolytic anemia and thrombocytopenia, with high exacerbation rates. This study examined all-cause and exacerbation-rela...
Neutropenia Through Enhanced Neutrophil Apoptosis and Secondary Necrosis in Wolfram Syndrome 1 [0.03%]
Wolfram综合征1通过增强的中性粒细胞凋亡和继发性坏死导致中性粒细胞减少症
Deniz Aslan,Handan Kayhan
Deniz Aslan
Primary Extra Nodal Natural Killer/T-cell Lymphoma (ENKTCL) of the CNS - A Rare Case Report with Diagnostic and Management Challenges [0.03%]
中枢神经系统原发性NK/T细胞淋巴瘤(NK/T细胞淋巴瘤)一例报告及诊断治疗难点分析
Surbhi Dahiya,Sabina Langer,Amrita Saraf et al.
Surbhi Dahiya et al.
AML with t(8;21): A Molecularly Defined Entity with Morphological Ambiguities [0.03%]
t（8；21）阳性急性髓系白血病：形态学特征模糊而分子生物学特征明确的实体
Smeeta Gajendra,Leena Gupta,Rani Sahoo
Smeeta Gajendra
Expression of Immune Checkpoints LAG-3, CTLA-4, TIM-3 and PD-1 in Beta Thalassemia patients Treated using HbF Augmentation Therapy and Regular Transfusions [0.03%]
用于治疗输血依赖型β-地中海贫血的去铁和加用促红细胞生成素(EPO)方案对免疫检查点LAG-3、CTLA-4、TIM-3及PD-1表达的影响研究
Komal Khan,Umaima Khan,Asma Shah et al.
Komal Khan et al.
Introduction: Beta-thalassemia is an inherited hemoglobin disorder caused by mutations in HBB gene encoding beta globin chains. Severe anemia secondary to defective globin chains, chronic hemolysis and ineffective erythro...