搜索结果: 1-14 共查到“医学 Sickle cell”相关记录14条 . 查询时间(0.043 秒)
“Spleen-on-a-chip” yields insight into sickle cell disease（图）
镰状细胞病 微流体装置 脾脏
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2023/6/5
Every day, billions of red blood cells pass through the spleen, an organ that is responsible for filtering out old or damaged blood cells. This task is made more difficult when the blood cells are mis...
Use of Continuous Regional Anesthetic for Management of Pediatric Sickle Cell Crisis
Sickle Cell Crisis Regional Anesthesia Pediatric Pain
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2013/1/30
Sickle cell patients often find difficulty obtaining adequate treatment of pain. Anti-inflammatory medications, steroids, and opioids can reduce pain; however their use is limited by side effects. We ...
First Presentation of Sickle Cell Anemia in A 3.5-Year-Old Girl:A Case Report
Sickle Cell Anemia
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2015/9/25
Sickle cell disease is an inherited disorder of hemoglobin synthesis, which affects many individuals worldwide. Vaso-occlusive, aplastic and sequestration crises are common in a sickle cell child.1 On...
Nitric Oxide and Trace Metals in Relation to Haemoglobin F Concentration in Nigerian Sickle Cell Disease Patients
Sickle cell disease trace metals haemoglobin F oxidants
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2010/2/24
Sickle cell disease (SCD) is an inherited haemoglobin (Hb) disorder associated with vaso-occlusive events, oxidative stress, high energy demand, and endothelial dysfunction. The endothelium plays a ce...
Humoral immunity and haemoglobin F (HbF) status in steady state adult Nigerian sickle cell disease patients with asymptomatic malaria
Sickle cell disease malaria parasitaemia immunoglobulins inflammation haemolysis
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2010/1/11
Aim: Nigeria, where malaria is prevalent, has the largest sickle cell gene pool in the world. To this end, there is a need for increased understanding of the pathophysiology of HbSS patients in a mala...
Sickle cell hemoglobin D disease First reported case in IRAN
Sickle cell hemoglobin D IRAN
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2009/12/15
A case of sickle cell Hb D disease IS reported in young Iranian male.the father of whom carried an AS sickle cell trait and the mother an AD trait.This disease was diagnosed by Hb electrophoresis.aga...
Many sickle-cell deaths in Africa may be avoidable
sickle-cell deaths Africa bacterial infections
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2009/9/15
Children in Africa with sickle cell anaemia are dying unnecessarily from bacterial infections, suggests the largest study of its kind, led by Oxford University researchers. The study, funded by the We...
Hyperbaric Oxygen Therapy in the Treatment of Sickle Cell Leg Ulcers
Sickle Cell wound healing
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2009/5/8
Rudge FW. Hyperbaric Oxygen Therapy in the Treatment of Sickle Cell Leg Ulcers. J. Hyperbaric Med 1991; 6(1):1-4.
Amelioration of Sickle Cell Crises With Intensive Hyperbaric Oxygen
Sickle Cell Hyperbaric Oxygenation
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2009/5/8
Hart GB, Finklestein JZ, Groncy PK, Meyer GW, Strauss MB. Amelioration of Sickle Cell Crises With Intensive Hyperbaric Oxygen. J. Hyperbaric Med 1991; 6(2):75-85.
Orthodontic Treatment of Patients with Sickle-cell Anemia
Orthodontic Treatment Patients Sickle-cell Anemia
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2008/11/17
Sickle-cell anemia is a genetic blood disease characterized by a hemoglobin gene mutation. The genetic failure is basically constituted by replacement of the hemoglobin beta chain in the sixth posit...
Equation to estimate resting energy expenditure in adolescents with sickle cell anemia
Resting energy expenditure sickle cell anemia prediction equations adolescents African Americans
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2016/12/20
Background: Basal energy requirements are higher in adolescents with sickle cell anemia (SCA) than in healthy control subjects. However, no equation is available to accurately predict their energ...
Body composition in children with sickle cell disease
Sickle cell disease growth nutritional status body composition children African Americans
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2016/12/19
Background: Impaired growth, poor nutritional status, and delayed skeletal and sexual maturation are common in children with sickle cell disease (SCD), yet the nature of associated body-compositi...
Energy intake and resting metabolic rate in preschool Jamaican children with homozygous sickle cell disease
Energy intake resting metabolic rate sickle cell disease children Jamaica weighed food intake
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2016/12/17
Background: A relative energy deficiency consequent to a high resting metabolic rate (RMR) may contribute to growth impairment in persons with homozygous (SS genotype) sickle cell disease (S...
Effect of zinc supplementation on growth and body composition in children with sickle cell disease
Sickle cell disease zinc supplementation growth body composition children
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2016/12/17
Background: Poor growth and delayed maturation in children with sickle cell disease (SCD) may be due, in part, to mild zinc deficiency.Objective: The objective was to determine the effects o...