An Increased Plasma D-Dimer Levels During Different Stages of Normal and Complicated Pregnancies Among Women in Bisha, Saudi Arabia [0.03%]
沙特阿拉伯贝沙妇女不同妊娠阶段正常妊娠和复杂妊娠的血浆D-二聚体水平变化研究
Tareg M Belali
Tareg M Belali
Introduction: Hypercoagulability is one of the most reported state among Pregnant women. During pregnancy, the concentrations of D-dimer increase in a trimester-dependent- manner. The presence of gestational diabetes (GD)...
The Value of Using Bedside Point of Care Testing for International Normalized Ratio in Patients on Warfarin Undergoing Dental Procedures and Bleeding Assessment; A Single Center Prospective Study [0.03%]
国际正常化比率的床旁检测在华法林抗凝患者牙科操作和出血评估中的应用价值：一项单中心前瞻性研究
Abdullah Albarkheel,Hawazen Alshareef,Amal Albar et al.
Abdullah Albarkheel et al.
Introduction: Postoperative bleeding is a significant complication in dental surgeries, especially for patients on anticoagulants. Risk stratification based on patient factors can help reduce these complications, but curr...
Robert Seby,Benjamin J McCormick,Emily Wolf et al.
Robert Seby et al.
Microangiopathic hemolytic anemia with associated multiorgan failure is a medical emergency. The differential diagnosis for microangiopathic hemolytic anemia is broad and requires a systematic, focused approach at ruling out serious causes....
Utilization of Fetal Hemoglobin Parameters in Predicting Clinical Severity of Sickle Cell Disease: Retrospective Study From a Tanzanian Cohort [0.03%]
坦桑尼亚队列的回顾性研究：利用胎儿血红蛋白参数预测镰状细胞疾病临床严重性的应用
Hadiya M Haji,Florence Urio,Siana Nkya et al.
Hadiya M Haji et al.
Background: Fetal hemoglobin (HbF) is found at a measurable amount in red blood cells (RBCs) called F cells. High fetal hemoglobin (HbF) levels are linked with milder forms of sickle cell disease (SCD). However, some pati...
Real-World Treatment Patterns, Clinical Outcomes, and Costs in Patients with Higher-Risk Myelodysplastic Syndromes Across France, Germany, and the United Kingdom [0.03%]
法国、德国和英国高危骨髓增生异常综合征患者的现实世界治疗模式、临床结局和成本研究
Mark Drummond,Carlo Finelli,Fjoralba Kristo et al.
Mark Drummond et al.
Background: Higher-risk myelodysplastic syndromes (HR-MDS) are associated with increased progression to acute myeloid leukemia (AML) and poor prognosis. P...
Effect of Haplo-Allogeneic Hematopoietic Stem Cell Transplantation Timing on Patients with Severe Aplastic Anemia Without Histocompatible Matched Sibling Donor [0.03%]
无全相合供者重症再生障碍性贫血患者行单倍型移植的移植时机探讨
Dan Fan,Fang Xiao,Jiayi Zhao et al.
Dan Fan et al.
Background: Comparative studies on frontline haploidentical HSCT (haplo-HSCT) versus salvage haplo-HSCT after immunosuppressive therapy (IST) failure in severe aplastic anemia (SAA) are limited. To evaluate the effects of...
Thrombotic Thrombocytopenic Purpura and Evans Syndrome: Validating and Exploring 20 Years of Routine Hospital Care [0.03%]
验证并探索 thrombotic thrombocytopenic purpura 和 Evans 综合征 20 年的常规医院治疗方案
Dana Audrey Lawrie,Dennis Lund Hansen,Thomas Leineweber Kristensen et al.
Dana Audrey Lawrie et al.
Purpose: Few patients scattered among centers complicate investigation of thrombotic thrombocytopenic purpura (TTP) and Evans syndrome (ES). Routinely collected Danish register data captures the total population and inclu...
Transplantation of Human Peripheral Stem and Progenitor Cells to Humanized Mouse Model for Systemic Lupus Erythematosus [0.03%]
人外周血干细胞和基质细胞向系统性红斑狼疮人源化小鼠移植
Syahrul Chilmi,Dina Fauziah,Matthew Brian Khrisna et al.
Syahrul Chilmi et al.
Introduction: Systemic Lupus Erythematosus (SLE) is an autoimmune disease characterized by damaged and dysregulated immune system due to breakdown in the selection process during clonal growth of immune cells. Studies hav...
Aplastic Anaemia Disease Burden From the Patient Perspective and Quality of Life in Zimbabwe by A. Maramba and J. Mupini [0.03%]
津巴布韦 aplasia 患者负担及生活质量研究
Aaron Maramba,Joice Mupini,Shungu Munyati et al.
Aaron Maramba et al.
Purpose: Aplastic Anaemia (AA) is a critical haematological disorder characterized by pancytopenia and marrow hypoplasia. It is generally regarded as a rare disease albeit with multiple symptoms. The aim of the study was ...
Real-World Evidence on Joint Condition in Non-Severe Hemophilia A Patients: A Multicenter Study [0.03%]
一项关于非重度A型血友病关节状态的真实世界证据的多中心研究
Ana Marco-Rico,José Manuel Calvo-Villas,Francisco-José López-Jaime et al.
Ana Marco-Rico et al.
Purpose: Patients with non-severe hemophilia A (PwnSHA) may be at risk for joint damage (JD), yet data remain scarce. Our aim was to evaluate the joint condition in PwnSHA in a real-world setting. ...