Anemia, Sickle CellIncidenceCase-Control StudiesRetrospective StudiesAdultMiddle AgedAcute Kidney InjuryGeorgiaFemaleThe purpose of this paper was to review the research examining the epidemiology of and costs associated with sickle cell anaemia (SCA). Although there is general acceptance that Black ...
SICKLE CELL ANEMIA: REPORT OF A CASE GREATLY IMPROVED BY SPLENECTOMY. EXPERIMENTAL STUDY OF SICKLE CELL FORMATION From these comprehensive and instructive studies, which are largely and fruitfully experimental, the authors come to regard the phenomenon of sideling of t... EV Hahn,EB Gillespie - ...
Case Studies in Assisted Reproduction: One partner is a carrier of thalassemia, one a carrier of sickle cell anemia 来自 Semantic Scholar 喜欢 0 阅读量: 4 作者: H Fatemi DOI: 10.1017/CBO9781139794671.011 年份: 2015 收藏 引用 批量引用 报错 分享 ...
Although sickle cell anaemia has been referred to as the ‘first molecular disease’[1] and paved the way to modern molecular biology, its management has lagged behind other subsequently described molecular disorders. For decades the management of sickle cell pain, the hallmark of sickle cell anaem...
The researchers conducted matched case-control and self-controlled case series studies of a retrospective cohort of children aged 6 months to 17 years in 8 managed care organizations that make up the Vaccine Safety Datalink (VSD) with a diagnosis of sickle cell anemia during influenza season (fro...
Figure 1: Sickle-cell anemia is characterized by deformed red blood cells. A sickle-shaped red blood cell is shown among a group of healthy red blood cells. A change in a single amino acid in one of the hemoglobin proteins is responsible for causing the abnormal sickle shape of this red ...
Sickle cell anemia: the legacy of the patient (Walter Clement Noel), the interne (Ernest Irons), and the attend- ing physician (James Herrick) and the facts of its discovery. Pediatr Radiol 2001;31:889–90. 3. Savitt TL, Goldberg MF. Herrick's 1910 case report of sickle cell ...
Sickle cell anemia (Hb SS) accounts for 60% to 70% of sickle cell disease in the United States. The other forms of sickle cell disease result from coinheritance of Hb S with other abnormal globin β-chain variants (Vichinsky and Schlis, 2006). Silent infarcts occur in the distribution ...
Sickle Cell Anemia Sickle cell is a homogenous genetic anemia caused when an abnormal gene (hemoglobin S or HbS) causes the substitution of the amino acid valine, for another, glutamic acid (Amundsen et al., 1984). The sickle gene protects heterogeneous carriers (HbC) from P. falciparum in ...
This chapter presents a case study of a 17﹜ear﹐ld boy with sickle cell anemia presented to the emergency department after developing a fever of 40 degree... S Konieczki,K Hamann - Cases in Pediatric Acute Care 被引量: 0发表: 2020年 Poor Sensitivity of Physician Assessment to Predict Acu...