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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:1.7/Q3

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共收录本刊相关文章索引1521
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
Timothy M Bahr,Archana M Agarwal,Jessica A Meznarich et al. Timothy M Bahr et al.
In North America, jaundiced neonates are not usually tested for G6PD deficiency if the family is of European ancestry. However, we describe such a family where ≥35 males have had severe (Class I) G6PD deficiency. Many of the jaundiced neon...
David H Vandorpe,Alicia Rivera,Boris E Shmukler et al. David H Vandorpe et al.
The molecular identity of Psickle, the deoxygenation-activated cation conductance of the human sickle erythrocyte, remains unknown. We observed in human sickle red cells that inhibitors of TRPA1 and TRPV1 inhibited Psickle, whereas a TRPV1 ...
Angelo Gardellini,Francesca Guidotti,Maddalena Feltri et al. Angelo Gardellini et al.
Glucocorticoid treatment is the standard initial therapy for patients with immune thrombocytopenia (ITP). Despite a rate of 60-80% of initial remissions, only 30 to 50% of adults have a sustained response after discontinuation. Second line ...
Zachary Weber,Ashley Sam,Alejandra Pena et al. Zachary Weber et al.
Abnormally high serum ferritin levels have been reported during pediatric ECMO, attributed to frequent red blood cell transfusion and suggestive of iron overload. However, the utility of ferritin for diagnosing iron overload is complicated ...
Crawford Strunk,Immacolata Tartaglione,Connie M Piccone et al. Crawford Strunk et al.
Background: Sickle cell disease (SCD) is characterized by frequent, unpredictable pain episodes and other vaso-occlusive crises (VOCs) leading to significant healthcare utilization. VOC frequency is often an endpoint in c...