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期刊名:Blood cells molecules and diseases

缩写:BLOOD CELL MOL DIS

ISSN:1079-9796

e-ISSN:1096-0961

IF/分区:2.1/Q3

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共收录本刊相关文章索引1537
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
Bita Asghariastanehei,Philippe Connes,Romain Carin et al. Bita Asghariastanehei et al.
Voxelotor, a hemoglobin S polymerization inhibitor, has been shown to reduce anemia in sickle cell anemia (SCA) but its effects on vaso-occlusive crisis frequency are limited. Its recent market withdrawal due to concerns over treatment-rela...
Philippe Connes,Marie Martin,Judith Catella et al. Philippe Connes et al.
Blood viscosity is recognized as a key determinant in the pathophysiology of vaso-occlusive crises (VOC) in sickle cell anemia (SCA). However, its longitudinal relationship with changes in VOC frequency over time remains poorly understood. ...
Jinrong Zhao,Xiaowei Chen,Liangliang Wu et al. Jinrong Zhao et al.
Circadian rhythms regulate immune cell activity, but their impact on hematopoietic stem cell infusion remains unclear. This retrospective study evaluated 177 severe aplastic anemia (SAA) patients undergoing unrelated donor hematopoietic ste...
Arwa Fraiwan,Bernard E Ebruke,Abubakar Gezawa et al. Arwa Fraiwan et al.
Sickle Cell Disease (SCD), a genetic blood disorder, claims the lives of thousands of young children in Africa every year. The World Health Organization estimates that 75% of the diagnosed cases of the disease are within sub-Saharan Africa ...
Kim G Lieu,Sabine Pestel,Mhairi Maxwell et al. Kim G Lieu et al.
A recombinant VWF D'D3 albumin fusion protein (rD'D3-FP) has been developed to extend the half-life of co-administered coagulation factor VIII (FVIII) for the treatment of haemophilia A. We examined the impact of albumin fusion of rD'D3 on ...
Sandhya Gupta,Nita Radhakrishnan,Archit Pandharipande et al. Sandhya Gupta et al.
Background: Heavy menstrual bleeding (HMB) a common manifestation of bleeding disorders in adolescents contributes to anemia, transfusions, and impaired quality-of-life (QOL). Evidence supporting practical management stra...
Antonella Meloni,Laura Pistoia,Paolo Ricchi et al. Antonella Meloni et al.
We quantified hepatic fat fraction (FF) by magnetic resonance imaging (MRI) in non-transfusion-dependent thalassemia (NTDT) patients, and we evaluated its associations with demographic, clinical, and biochemical parameters, tissue iron over...
Kamal Kumar Meher,Pradeep Kumar Mohanty,Satyabrata Meher Kamal Kumar Meher
Sickle cell disease (SCD) is a monogenic blood disorder in which vaso-occlusive crises (VOC) are the main cause of hospitalization. Along with vascular adhesion, inflammation plays a central role in VOC. This study compared inflammatory and...