Haller, J.O., W.E. Berdon, and H. Franke, Sickle cell anemia: the legacy of the patient (Walter Clement Noel), the interne (Ernest Irons), and the attending physician (James Herrick) and the facts of its discovery. Pediatr Radiol., 2001; 31(12):889-90 PMID:11727028...
SICKLE cell anemiaPATIENT-controlled analgesiaOPIOIDSPATIENTSLooks at sickle cell disease (SCD) patients' perceptions of self-administering parenteral opioids. Overview of SCD; Relationship between pain and SCD; Patient-identified advantages of self-administering analgesia in the hospi...
Sickle cell anemia (SCA) is associated with a chronic proinflammatory state characterized by elevated leukocyte count, mortality from severe recurrent infections, and subsequent vasoocclusive complications with leukocyte adhesion to the endothelium and increased plasma levels of inflammatory cytokines. The ...
sickle cell anemia 听听怎么读 英[ˈsɪkəl sel əˈni:mi:ə] 美[ˈsɪkəl sɛl əˈnimiə] 是什么意思 n. 镰状细胞血症; 学习怎么用 权威例句 Treatment of sickle cell anemia mouse model with iPS cells generated from autologous skin....
A Rochester woman who was born with sickle-cell anemia has been cured of the disease after a bone marrow transplant at the University of Rochester Medical Center.
Additional points to remember are the psychological aspects of this disease: (1) There is no satisfactory treatment and no cure for sickle-cell anemia; (2) the patient generally does not live past the age of 40 years; and (3) the patient usually succumbs to a crisis, either aplasia, ...
Sickle cell disease or sickle cell anemia is the most common of the hereditary blood disorders among black people of African descent worldwide. Learn about symptoms, treatment, causes, inheritance, testing, complications, and more.
Although it also gives information useful to doctors, caregivers and other health professionals, it tells patients where and how to look for information covering virtually all topics related to sickle cell anemia (also Hb S disease; Hemoglobin S dis... (展开全部) 我来说两句 短评 ··· 热门...
The response to hydroxyurea is variable and unpredictable from patient to patient. Hydroxyurea can be suppressive to the bone marrow. Dactylitis and arthritis Swelling and inflammation of the hands and/or feet is often an early sign of sickle cell anemia. The swelling involves entire fingers and/...
The case involves a 38‐year‐old female of Nigerian descent with sickle cell anemia (SCA, βS/βS genotype), no α‐globin gene deletion and no glucose 6‐phosphate dehydrogenase deficiency. Over the past two decades, the patient received routine care at the National Institutes of Health (...