首页 文献索引 SCI期刊 AI助手
期刊目录筛选

期刊名:Ejhaem

缩写:

ISSN:2688-6146

e-ISSN:2688-6146

IF/分区:1.2/Q4

文章目录 更多期刊信息

共收录本刊相关文章索引1303
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
Liya Ma,Yaojia Shen,Jie Chang et al. Liya Ma et al.
We report a 69-year-old man diagnosed as myelodysplastic syndrome and administrated with azacitidine and selinexor treatment. Then he was revealed high fever and multiple tender erythematous papules involving his mouth, back, upper and lowe...
Carla Romagnoli,Alexandra Lyubimova,Leily Santos-Carrion et al. Carla Romagnoli et al.
Hemophagocytic lymphohistiocytosis (HLH) is an immune disorder causing excessive inflammation and tissue damage. Lymphoma, especially T-cell lymphoma, is the most common cause of HLH, while Multiple Myeloma (MM) is rarely associated. We pre...
Rosa María González Arreola,María Teresa Magaña Torres,Ma Guadalupe Domínguez Quezada et al. Rosa María González Arreola et al.
Introduction: In Mexico, the 5-year overall survival (OS) rate for pediatric acute lymphoblastic leukemia (ALL) ranges from 45% to 85%, markedly lower than the ∼90% reported in high-income countries, where cytogenomic te...
Mayu Tomita,Natsumi Kawasaki,Keigo Yorozu et al. Mayu Tomita et al.
Introduction: Polatuzumab vedotin (Pola) is an antibody-drug conjugate approved for the treatment of diffuse large B-cell lymphoma (DLBCL). Several reports suggest that the tumor microenvironment influences the outcome of...
Bo Zhang,Olga K Weinberg,Weina Chen et al. Bo Zhang et al.
Background: Immunophenotypically defined mixed-phenotype acute leukemias (MPAL) are rare and remain a diagnostic and therapeutic dilemma. We aim to explore the clinicopathologic characteristics and oncological outcomes of...
Tomotaka Suzuki,Rui Yokomori,Takaomi Sanda et al. Tomotaka Suzuki et al.
Secondary plasma cell leukemia (sPCL) is a rare, aggressive manifestation of multiple myeloma (MM). We report a 75-year-old Japanese man with anemia as the chief complaint and IgG-λ MM that rapidly progressed to sPCL. Whole genome sequenci...
[This corrects the article DOI: 10.1002/jha2.70170.]. © 2026 The Author(s). eJHaem published by British Society for Haematology and John Wiley & Sons Lt...