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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:2.1/Q3

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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
Martha Amoding,Joachim Ndawula,Bright Hajusu et al. Martha Amoding et al.
Purpose: This study aimed to determine the prevalence, morphological classification, and factors associated with anemia among neonates at Soroti Regional Referral Hospital neonatal unit. ...
Katsuyoshi Koh,Keiji Nogami,Harumi Kakuda et al. Katsuyoshi Koh et al.
Purpose: Severe congenital protein C deficiency (SCPCD) is a rare, life-threatening disorder. Plasma-derived protein C concentrate is recommended for the acute and long-term management of SCPCD; however, data in Japanese ...
Harneet Kaur,Debjit Ghoshal,Inderpreet Singh Khurana Harneet Kaur
Background: Thrombotic thrombocytopenic purpura (TTP) is a life-threatening blood disorder resulting from ADAMTS13 deficiency, caused by mutations in the ADAMTS13 gene in congenital TTP (cTTP), and by neutralizing antibod...
Marc Bienz,Monika Oliver,Catherine Sperlich et al. Marc Bienz et al.
The treatment of patients with PNH has been revolutionized by terminal complement C5 inhibitors, which control intravascular hemolysis and thrombosis, reduce morbidity and mortality, and improve life expectancy to that approaching people wi...
Rebecca Winkler,Ishan Herath,Radoslaw Kaczmarek et al. Rebecca Winkler et al.
In the last few years, gene therapy, holding the promise for long-term disease correction through a one-time treatment, has transitioned from experimental research to approved medicine. Several gene therapies are now available for congenita...
Silvia Awor,Jimmyy Opee,Denis Ocaya et al. Silvia Awor et al.
Background: Sickle cell disease (SCD) is a genetic blood disorder most prevalent in Eastern and Western Africa. With the high prevalence of SCD in northern Uganda, we set out to document the haematological profile of pati...
Siting Wu,Chunli Wang,Dan Li et al. Siting Wu et al.
Hemophilia is a lifelong coagulation disorder with varying severity levels, which significantly impacts management strategies. The transition period from pediatric to adult medical system represents a critical stage for ensuring continuous ...
Kailei Du,Maofeng Wang,Ping Yu Kailei Du
Objective: Third-generation cephalosporins are widely used for severe infections but carry thrombocythemia risks complicating therapeutic decisions. Current predictive tools lack accuracy and clinical interpretability. Th...
Lou&#x;i Al-Husinat,Fadi Haddad,Sarah Al Sharie et al. Lou&#x;i Al-Husinat et al.
Background: Blood transfusion during hip fracture surgery can significantly influence patient outcomes. This study aimed to identify risk factors for post-operative blood transfusions and their impact on clinical outcomes...
Junling Han,Hongmei Niu,Fuqian Zhao et al. Junling Han et al.
Background: Incompatible cross-matching at room temperature can delay critical blood transfusions. We report that red cells from patients requiring blood transfusion agglutinated after cross-matching at room temperature, ...