Musculoskeletal manifestations of sickle cell anaemia: a pictorial review [0.03%]
镰状细胞贫血的肌肉骨骼系统表现：一组病例回顾
A Ganguly,W Boswell,H Aniq
A Ganguly
Sickle cell anaemia is an autosomal recessive genetic condition producing abnormal haemoglobin HbS molecules that result in stiff and sticky red blood cells leading to unpredictable episodes of microvascular occlusions. The clinical and rad...
Kathryn Blake,John Lima
Kathryn Blake
Objective. To review issues related to asthma in sickle cell disease and management strategies. Data Source. A systematic review of pertinent original research publications, reviews, and editorials was undertaken using MEDLlNE, the Cochrane...
Relationship between Painful Crisis and Serum Zinc Level in Children with Sickle Cell Anaemia [0.03%]
镰状细胞贫血患儿疼痛危象与血清锌水平的关系
Edamisan Olusoji Temiye,Edem Samuel Duke,Mbang Adeyemi Owolabi et al.
Edamisan Olusoji Temiye et al.
Sickle cell anaemia (SCA) is associated with zinc deficiency; zinc supplementation may ameliorate some of its clinical manifestations including the relief of painful crisis. Subjects and Methods. Serum zinc levels were determined in 71 chil...
Role of calcium in phosphatidylserine externalisation in red blood cells from sickle cell patients [0.03%]
钙在镰状细胞病患者红细胞中磷脂酰丝氨酸外翻作用中的角色
Erwin Weiss,David Charles Rees,John Stanley Gibson
Erwin Weiss
Phosphatidylserine exposure occurs in red blood cells (RBCs) from sickle cell disease (SCD) patients and is increased by deoxygenation. The mechanisms responsible remain unclear. RBCs from SCD patients also have elevated cation permeability...
Priapism in sickle cell anemia: emerging mechanistic understanding and better preventative strategies [0.03%]
镰状细胞贫血症阴茎异常勃起的新认识和预防策略
Genevieve M Crane,Nelson E Bennett Jr
Genevieve M Crane
Sickle cell anemia is a common and disabling disorder profoundly affecting mortality as well as quality of life. Up to 35% of men with sickle cell disease are affected by painful, prolonged erections termed ischemic priapism. A priapic epis...
Community-based screening for infantile anemia in an okinawan village, Japan [0.03%]
日本冲绳一个村庄的社区婴儿贫血筛查项目
Tomiko Hokama,Chiemi Yogi,Colin W Binns et al.
Tomiko Hokama et al.
Infancy is a vulnerable age group for anemia throughout the world. However, community-based screening for infantile anemia is seldom reported. This study determined the prevalence of anemia among infants in an Okinawan village from 2003 to ...
The Properties of Red Blood Cells from Patients Heterozygous for HbS and HbC (HbSC Genotype) [0.03%]
HbS与HbC杂合子（HbSC基因型）患者的红细胞特性分析
A Hannemann,E Weiss,D C Rees et al.
A Hannemann et al.
Sickle cell disease (SCD) is one of the commonest severe inherited disorders, but specific treatments are lacking and the pathophysiology remains unclear. Affected individuals account for well over 250,000 births yearly, mostly in the Tropi...