Factor V Leiden G1691A and prothrombin G20210A mutations among Palestinian patients with sickle cell disease [0.03%]
β-地中海贫血患者的F5和PROTM基因突变检测及其临床意义
Fekri Samarah,Mahmoud A Srour
Fekri Samarah
Background: Vascular thrombosis is an important pathophysiological aspect of sickle cell disease (SCD). This study aimed to investigate the prevalence and clinical impact of factor V Leiden G1691A (FVL) and prothrombin G2...
A novel fibrinogen mutation: FGA g. 3057 C > T (p. Arg104 > Cys) impairs fibrinogen secretion [0.03%]
一种新的纤维蛋白原突变：FGA g. 3057 C > T（p. Arg104 > Cys）影响纤维蛋白原分泌
R Marchi,M Linares,H Rojas et al.
R Marchi et al.
Background: Abnormal fibrinogens can be caused by clinically silent hereditary mutations. A new case was detected accidentally in an 11-year-old girl when routine pre-operative coagulation tests were performed for nasal t...
A comparative cross-sectional study of some hematological parameters of hypertensive and normotensive individuals at the university of Gondar hospital, Northwest Ethiopia [0.03%]
一项在埃塞俄比亚北部贡达尔大学医院进行的高血压患者与正常血压患者的某些血液学参数比较横断面研究
Bamlaku Enawgaw,Nigist Adane,Betelihem Terefe et al.
Bamlaku Enawgaw et al.
Background: Hypertension is a major health problem worldwide. It can lead to cardiovascular disease and also leads to functional disturbances including hematological parameters. The abnormalities of haematological paramet...
Knowledge, attitude and practice of students towards blood donation in Arsi university and Adama science and technology university: a comparative cross sectional study [0.03%]
亚си大学和阿达玛科技大学学生献血知识、态度及行为差异的比较性横断面研究
Habtom Woldeab Gebresilase,Robera Olana Fite,Sileshi Garoma Abeya
Habtom Woldeab Gebresilase
Background: Blood can save millions of lives. Even though people do not donate blood regularly, there is a constant effort to balance the supply and demand of blood. The aim of this study was, therefore, to determine the ...
Emergency blood transfusion practices among anaemic children presenting to an urban emergency department of a tertiary hospital in Tanzania [0.03%]
坦桑尼亚三级医院城市急诊科贫血儿童紧急输血实践状况
Catherine R Shari,Hendry R Sawe,Brittany L Murray et al.
Catherine R Shari et al.
Background: Severe anaemia contributes significantly to mortality, especially in children under 5 years of age. Timely blood transfusion is known to improve outcomes. We investigated the magnitude of anaemia and emergency...
Coagulation profile of Sudanese children with homozygous sickle cell disease and the effect of treatment with omega-3 fatty acid on the coagulation parameters [0.03%]
苏丹β-海洋性贫血和镰刀形红细胞性状同基因型患儿凝血状况及其ω-3脂肪酸治疗效果分析
Shiekh Awoda,Ahmed A Daak,Nazik Elmalaika Husain et al.
Shiekh Awoda et al.
Background: It has been reported that patients with SCD do have an abnormal coagulation profile. Coagulopathy is thought to be one of the key factors that contribute to the vaso-occlusive crisis that characterises sickle ...
Prevalence and determinants of anemia among pregnant women in Ethiopia; a systematic review and meta-analysis [0.03%]
埃塞俄比亚孕妇贫血的流行率及影响因素：系统评价和 Meta 分析
Getachew Mullu Kassa,Achenef Asmamaw Muche,Abadi Kidanemariam Berhe et al.
Getachew Mullu Kassa et al.
Background: Anemia during pregnancy is one of the most common indirect obstetric cause of maternal mortality in developing countries. It is responsible for poor maternal and fetal outcomes. A limited number of studies wer...
Significantly elevated foetal haemoglobin levels in individuals with glucose 6-phosphate dehydrogenase disease and/or sickle cell trait: a cross-sectional study in Cape Coast, Ghana [0.03%]
葡萄糖-6-磷酸脱氢酶缺陷症和/或镰状细胞性状个体中胎儿血红蛋白水平显著升高的横断面研究：加纳卡普海岸的研究结果
Patrick Adu,Essel K M Bashirudeen,Florence Haruna et al.
Patrick Adu et al.
Background: Previously published data have demonstrated that sickle red blood cells produce twice as much reactive oxygen species (ROS) suggesting that co-inheritance of sickle cell disease (SCD) and glucose 6-phosphate d...
Comparative study of sickle cell anemia and hemoglobin SC disease: clinical characterization, laboratory biomarkers and genetic profiles [0.03%]
镰形细胞贫血和HbSC病的比较研究：临床特征、实验室生物标志物及基因型分析
Milena Magalhães Aleluia,Teresa Cristina Cardoso Fonseca,Regiana Quinto Souza et al.
Milena Magalhães Aleluia et al.
Background: In this study, we evaluate the association of different clinical profiles, laboratory and genetic biomarkers in patients with sickle cell anemia (SCA) and hemoglobin SC disease (HbSC) in attempt to characteriz...
The frequency and severity of epistaxis in children with sickle cell anaemia in eastern Uganda: a case-control study [0.03%]
乌干达东部镰状细胞性贫血儿童鼻出血的发病率和严重程度：一项病例对照研究
Amina Nardo-Marino,Thomas N Williams,Peter Olupot-Olupot
Amina Nardo-Marino
Background: There are a paucity of data on epistaxis as it pertains to sickle cell anaemia. Some case studies suggest epistaxis to be a significant complication in patients with sickle cell anaemia in sub-Saharan Africa; ...