Real-world study on patient characteristics, treatment patterns and outcomes for treated patients with chronic lymphocytic leukemia during 2013-2022 in Finland [0.03%]
2013年至2022年芬兰慢性淋巴细胞白血病治疗患者的特点、治疗模式和结局的现实世界研究
Juha Ranti,Sanaz Jamalzadeh,Eleonora Mäkelä et al.
Juha Ranti et al.
The aim of this study was to describe the chronic lymphocytic leukemia (CLL) patient population characteristics, treatments, outcomes, and healthcare resource utilization (HCRU) in Finland. All adult patients diagnosed with CLL (ICD-10: C91...
Impact of inflammatory cytokine polymorphisms on the progression of myelodysplastic syndromes [0.03%]
炎症细胞因子多态性对骨髓增生异常综合征进展的影响
Nanami Gotoh,Tsatsralgerel Munkh-Erdene,Ai Hayashi et al.
Nanami Gotoh et al.
Chronic inflammation is increasingly recognized as a key contributor to tumorigenesis, promoting genomic instability, immune evasion, and malignant transformation. Inflammatory cytokines are particularly involved in the pathogenesis and pro...
The diagnosis and clinical characterization of -α3.7/--SEA thalassemia patients: two cases report [0.03%]
-α3.7/--SEA型地中海贫血的诊断及临床特征分析2例报告
Xiuling Wang,Yu Ding,Zhiyong Huang et al.
Xiuling Wang et al.
α-thalassemia is a hereditary hemolytic anemia, in which the clinical manifestations vary greatly depending on the degree of α-globin gene deletion. -α3.7/--SEA thalassemia is an intermediate type of α-thalassemia, with three α-globin ...
Late-onset hemophagocytic lymphohistiocytosis associated with monoallelic STX11 mutation in an adult: a case report and rationale for early allogeneic hematopoietic cell transplantation [0.03%]
STX11单等位基因突变成人患者晚发性噬血细胞性淋巴组织细胞增生症1例及早期异基因造血干细胞移植指征探讨
Jan Mateusz Zaucha,Andrzej Mital,Michał Taszner et al.
Jan Mateusz Zaucha et al.
Late-onset familial hemophagocytic lymphohistiocytosis (fHLH) remains a diagnostic and therapeutic challenge, particularly in adult patients presenting without a clear family history. We report a fatal case of HLH in a previously healthy ad...
Correction to: Evaluated NSUN3 in reticulocytes from HbH-CS disease that reflects cellular stress in erythroblasts [0.03%]
纠正：在反映红细胞系细胞应激的HbH-CS疾病中评估了网织红细胞中的NSUN3功能
Haodong Liu,Chunting Peng,Qisheng Su et al.
Haodong Liu et al.
Published Erratum
Annals of hematology. 2025 Sep 18. DOI:10.1007/s00277-025-06633-2 2025
Zhiyao Ren,Barbara De Moerloose,Tim Lammens
Zhiyao Ren
Long non-coding RNA (lncRNA) signatures have emerged as important prognostic biomarkers in acute myeloid leukemia (AML), stratifying patients into high-risk and low-risk groups and thus providing valuable insights for personalized treatment...
Survival analysis and prognosis model construction of elderly patients with acute promyelocyticleukemia: a retrospective study based on SEER database [0.03%]
基于SEER数据库的老年急性早幼粒细胞白血病患者的生存分析及预后模型构建研究
Jinhong Jiang,Yonghua Liu,Yuxiao Zeng et al.
Jinhong Jiang et al.
The survival and death cause in elderly acute promyelocytic leukemia (APL) patients were analyzed and a prognosis model was constructed. Retrospectively, the medical data of elderly APL patients (N = 1723, from year 2000 to 2020) were gaine...
T-cell acute lymphoblastic leukemia: therapeutic outcomes in adolescents and young adults [0.03%]
青少年和年轻成人T细胞急性淋巴细胞白血病的治疗结局
Emna Azza,Aya Ben Othmen,Maroua Bahri et al.
Emna Azza et al.
T-cell acute lymphoblastic leukemia (T-ALL) in adolescents and young adults (AYA) poses distinct clinical challenges. This study evaluates the effectiveness and tolerability of a pediatric-inspired regimen in this specific age group, focusi...
Challenges in accuracy in molecular genetic diagnosis of childhood AML: case series [0.03%]
儿童AML分子遗传诊断准确性挑战的病例系列分析
Fernanda de Oliveira Mota,Silva Regina Caminada de Toledo,Francine Tesser-Gamba et al.
Fernanda de Oliveira Mota et al.
Survival rate of children with Acute Myeloid Leukemia (AML) improves gradually through cooperative studies. However, the outcome depends on heterogeneous mechanisms. Comprehending the genetic background of pediatric Acute Myeloid Leukemia (...
Revisiting hepatitis B vaccination in children with transfusion-dependent thalassemia [0.03%]
输血依赖性地中海贫血儿童的乙肝疫苗接种问题再探讨
Angga Wirahmadi,Ludi Dhyani Rahmartani,Pustika Amalia Wahidiyat
Angga Wirahmadi
Thalassemia is a common hereditary hemoglobinopathy found largely in the "Thalassemia Belt". Thalassemia children are at risk of the hepatitis B virus (HBV) infection, given the frequent need for blood transfusions. The immune dysregulation...