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1
Studies on iron metabolism in sickle cell anaemia, sickle cell haemoglobin C disease, and haemoglobin C disease using a large volume liquid scintillation counter.使用大容量液体闪烁计数器对镰状细胞贫血、镰状细胞血红蛋白C病和血红蛋白C病中铁代谢的研究。
J Clin Pathol. 1970 Mar;23(2):127-34. doi: 10.1136/jcp.23.2.127.
2
Sickle-cell anaemia, sickle-cell thalassaemia, sickle-cell haemoglobin C disease, and asymptomatic haemoglobin C thalassaemia in one Ghanaian family.一个加纳家庭中的镰状细胞贫血、镰状细胞地中海贫血、镰状细胞血红蛋白C病和无症状血红蛋白C地中海贫血。
Br Med J. 1969 Mar 8;1(5644):607-12. doi: 10.1136/bmj.1.5644.607.
3
SIMULTANEOUS RADIOACTIVE TRACER STUDIES OF ERYTHROPOIESIS AND RED-CELL DESTRUCTION IN SICKLE-CELL DISEASE AND SICKLE-CELL HAEMOGLOBIN/THALASSAEMIA.镰状细胞病和镰状细胞血红蛋白/地中海贫血中红细胞生成与红细胞破坏的同步放射性示踪研究
Br J Haematol. 1963 Oct;9:487-98. doi: 10.1111/j.1365-2141.1963.tb05473.x.
4
Iron resorption in fish-induced anaemia in mink.
Nature. 1967 Jul 8;215(5097):187-8. doi: 10.1038/215187a0.
5
Organ iron accumulation in chronically transfused children with sickle cell anaemia: baseline results from the TWiTCH trial.镰状细胞贫血慢性输血患儿的器官铁蓄积:TWiTCH试验的基线结果
Br J Haematol. 2016 Jan;172(1):122-30. doi: 10.1111/bjh.13791. Epub 2015 Nov 2.
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An assessment of techniques suitable for the diagnosis of sickle-cell disease and haemoglobin C disease in cord blood samples.脐血样本中镰状细胞病和血红蛋白C病诊断适用技术的评估。
J Clin Pathol. 1970 Sep;23(6):533-7. doi: 10.1136/jcp.23.6.533.
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Bone marrow in sickle cell anaemia at time of anaemic crisis.镰状细胞贫血贫血危象时的骨髓。
Arch Dis Child. 1984 Jun;59(6):561-5. doi: 10.1136/adc.59.6.561.
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Iron studies in pregnant and non-pregnant women with haemoglobin SS or SC disease.
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Heme degradation and oxidative stress in murine models for hemoglobinopathies: thalassemia, sickle cell disease and hemoglobin C disease.血红蛋白病小鼠模型中的血红素降解与氧化应激:地中海贫血、镰状细胞病和血红蛋白C病
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Transfusion support for haemoglobinopathies.血红蛋白病的输血支持
Clin Haematol. 1984 Feb;13(1):151-65.

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Iron absorption in adults with sickle cell anemia: a stable-isotope approach.成人镰状细胞贫血的铁吸收:稳定同位素法。
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The effect of food and nutrients on iron overload: what do we know so far?食物和营养素对铁过载的影响:我们目前了解多少?
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Circ Res. 2015 Jan 16;116(2):298-306. doi: 10.1161/CIRCRESAHA.116.304577. Epub 2014 Nov 6.

本文引用的文献

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Studies in iron transportation and metabolism. IX. The excretion of iron as measured by the isotope technique.铁运输与代谢的研究。IX. 用同位素技术测定铁的排泄量。
J Lab Clin Med. 1955 Apr;45(4):599-615.
2
IRON ABSORPTION IN HYPOFERREMIA.缺铁血症中的铁吸收
Am J Med Sci. 1965 May;249:537-47. doi: 10.1097/00000441-196505000-00007.
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IRON-59 ABSORPTION MEASUREMENTS BY WHOLE-BODY COUNTING: STUDIES IN ALCOHOLIC CIRRHOSIS, HEMOCHROMATOSIS, AND PANCREATITIS.
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A NOTE CONCERNING THE "100 PER CENT VALUE" IN IRON ABSORPTION STUDIES BY WHOLE BODY COUNTING.
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HEMOGLOBIN C DISEASE. QUANTITATIVE DETERMINATION OF IRON KINETICS AND HEMOGLOBIN SYNTHESIS.血红蛋白C病。铁动力学和血红蛋白合成的定量测定。
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SIMULTANEOUS RADIOACTIVE TRACER STUDIES OF ERYTHROPOIESIS AND RED-CELL DESTRUCTION IN SICKLE-CELL DISEASE AND SICKLE-CELL HAEMOGLOBIN/THALASSAEMIA.镰状细胞病和镰状细胞血红蛋白/地中海贫血中红细胞生成与红细胞破坏的同步放射性示踪研究
Br J Haematol. 1963 Oct;9:487-98. doi: 10.1111/j.1365-2141.1963.tb05473.x.
7
The determination of iron absorption and loss by whole body counting.
Blood. 1962 Nov;20:517-31.
8
Sickle cell-hemoglobin C disease. Quantitative determination of iron kinetics and hemoglobin synthesis.镰状细胞-血红蛋白C病。铁动力学和血红蛋白合成的定量测定。
Blood. 1963 May;21:535-45.
9
Studies on congenital hemolytic syndromes, IV. Gastrointestinal absorption of iron.先天性溶血性综合征的研究,IV. 铁的胃肠道吸收
Blood. 1962 Mar;19:359-78.
10
A quantitative method for measuring the gastrointestinal absorption of iron.一种测量铁在胃肠道吸收情况的定量方法。
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使用大容量液体闪烁计数器对镰状细胞贫血、镰状细胞血红蛋白C病和血红蛋白C病中铁代谢的研究。

Studies on iron metabolism in sickle cell anaemia, sickle cell haemoglobin C disease, and haemoglobin C disease using a large volume liquid scintillation counter.

作者信息

Ringelhann B, Konotey-Ahulu F, Dodu S R

出版信息

J Clin Pathol. 1970 Mar;23(2):127-34. doi: 10.1136/jcp.23.2.127.

DOI:10.1136/jcp.23.2.127
PMID:5423947
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC474472/
Abstract

Iron absorption as measured by a faecal recovery method in young adult males living in a tropical zone was high, even in the absence of anaemia. There was an inverse relation between the iron absorption and the packed cell volume. The highest absorption was found in sickle cell anaemia patients, where the packed cell volume is the lowest. The incorporation of iron was also the fastest and greatest in this group. In the controls the iron absorbed accumulated in the marrow and the spleen on the first day; in the sickle cell anaemia group the spleen has an insignificant role in iron storage. The growing radioactivity in the liver parallels that of the heart in the group of sickle cell anaemia patients; however, it remains low in the spleen in the same group, implying a diminution of splenic blood flow. In the sickle cell haemoglobin C and the haemoglobin C patients, the liver and spleen have an intermediate position between that of the sickle cell anaemia group and the control group.

摘要

通过粪便回收法测量,生活在热带地区的年轻成年男性的铁吸收量很高,即使在没有贫血的情况下也是如此。铁吸收与红细胞压积之间呈负相关。镰状细胞贫血患者的铁吸收量最高,其红细胞压积最低。该组中铁的掺入也是最快且最多的。在对照组中,第一天吸收的铁积聚在骨髓和脾脏中;在镰状细胞贫血组中,脾脏在铁储存中作用不显著。镰状细胞贫血患者组中,肝脏放射性的增加与心脏同步;然而,同一组中脾脏的放射性仍然很低,这意味着脾血流量减少。在镰状细胞血红蛋白C和血红蛋白C患者中,肝脏和脾脏的情况介于镰状细胞贫血组和对照组之间。