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期刊名:Journal of blood medicine

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ISSN:1179-2736

e-ISSN:1179-2736

IF/分区:2.7/Q2

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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
Fjoralba Kristo,Sneha S Kelkar,Rutika Raina et al. Fjoralba Kristo et al.
Purpose: Limited real-world data exist on care patterns in peripheral T-cell lymphoma (PTCL) patients. We report care patterns and outcomes among PTCL patients in France, the United Kingdom (UK), Germany, and Italy in the...
Magdalena Wolowiec,Katarzyna Drabko,Lucyna Maciejka-Kemblowska et al. Magdalena Wolowiec et al.
Background: M-HLH is a type of HLH that most often occurs in children in the course of hematological malignancies. The diagnosis is based on meeting the criteria of the HLH-2004 Protocol. The disease has a rapid course, a...
Shehab Mohamed,Mohamad Wajeh Dulli,Abdulrahman Al-Mashdali et al. Shehab Mohamed et al.
Purpose: Hairy Cell Leukemia (HCL) is a rare, chronic B-cell lymphoproliferative neoplasm characterized by the accumulation of abnormal lymphocytes in the bone marrow and spleen. Although outcomes are generally favorable ...
Carmine Siniscalchi,Manuela Basaglia,Tiziana Meschi et al. Carmine Siniscalchi et al.
Catheter-related superficial venous thrombosis (SVT) of the upper extremity is a frequent complication of peripheral venous cannulation and longer peripheral devices such as midline catheters and peripherally inserted central catheters (PIC...
Qian Luo,Xuzhao Zhang,Xi Qiu et al. Qian Luo et al.
Teclistamab, a B-cell maturation antigen (BCMA) × CD3 bispecific T-cell engager, has shown significant efficacy in patients with refractory multiple myeloma (MM). However, the clinical characteristics and optimal management strategies for ...
Mona El-Ghamrawy,Marwa Abdelhady,Salma Mohamed Fathy Zahran et al. Mona El-Ghamrawy et al.
Background: Inherited bleeding disorders (IBDs) require accurate diagnosis and long-term management. This study characterized the clinical and hematologic profile of Egyptian children with IBDs managed at Cairo University...
Mengyuan Si,Shanghong Yang,Zijian Chen et al. Mengyuan Si et al.
Hereditary Spherocytosis (HS), with characteristic red blood cells (RBCs), is a group of genetic hemolytic disorders that occur in an autosomal-dominant manner. It is clinically characterized by anemia, splenomegaly, jaundice, and mutations...
Ivan Mugisha Taremwa,Nixon Niyonzima,Scholastic Ashaba et al. Ivan Mugisha Taremwa et al.
Background: Blood transfusions are essential in the supportive care of patients with hematological malignancies but carry a risk of adverse reactions. Data on the incidence of transfusion reactions remain scarce in Uganda...
Jun Ho Jang,Chul Won Jung,Dae-Ho Choi et al. Jun Ho Jang et al.
Background: Myelodysplastic syndromes comprise a diverse group of hematopoietic stem-cell malignancies characterized by ineffective hematopoiesis, cytopenia, and increased risk of acute myeloid leukemia. Anemia is a commo...