Dipyrrolic urinary pigments in congenital Heinz-body anaemia due to Hb köln and in thalassaemia.
作者信息
Kreimer-Birnbaum M, Pinkerton P H, Bannerman R M, Hutchison H E
出版信息
Br Med J. 1966 Aug 13;2(5510):396. doi: 10.1136/bmj.2.5510.396.
Abstract
摘要
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Dipyrrolic urinary pigments in congenital Heinz-body anaemia due to Hb köln and in thalassaemia.因血红蛋白科隆病和地中海贫血导致的先天性海因茨小体贫血中的双吡咯尿色素。
Br Med J. 1966 Aug 13;2(5510):396. doi: 10.1136/bmj.2.5510.396.
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Unstable hemoglobins and thalassemia: some properties of Hb Köln.
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[Influence of Heinz bodies on rheologic properties of patients with Heinz body anemia (hemoglobin Köln)].
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Mechanisms of Heinz body formation and attachment to red cell membrane.海因茨小体形成及附着于红细胞膜的机制。
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Altered sulfhydryl reactivity of hemoglobins and red blood cell membranes in congenital Heinz body hemolytic anemia.先天性 Heinz 小体溶血性贫血中血红蛋白和红细胞膜巯基反应性的改变
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[Hb frankfurt: a new unstable haemoglobin as the cause of Heinz-body anaemia in a German family].[血红蛋白法兰克福：一种新的不稳定血红蛋白，为德国家庭中亨氏小体贫血的病因]
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Congenital Heinz-body haemolytic anaemia due to haemoglobin Hammersmith.由于血红蛋白汉默史密斯型导致的先天性海因茨小体溶血性贫血。
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The role of hemoglobin heme loss in Heinz body formation: studies with a partially heme-deficient hemoglobin and with genetically unstable hemoglobins.血红蛋白血红素丢失在亨氏小体形成中的作用：使用部分血红素缺乏的血红蛋白和遗传不稳定血红蛋白的研究
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[Congenital hemolytic Heinz body anemia with instable hemoglobins].
Monatsschr Kinderheilkd (1902). 1976 May;124(5):310-2.
引用本文的文献
1
Congenital Heinz-body haemolytic anaemia due to haemoglobin Hammersmith.由于血红蛋白汉默史密斯型导致的先天性海因茨小体溶血性贫血。
Postgrad Med J. 1969 Sep;45(527):629-32. doi: 10.1136/pgmj.45.527.629.
2
Catabolism of heme in vivo: comparison of the simultaneous production of bilirubin and carbon monoxide.体内血红素的分解代谢：胆红素与一氧化碳同时生成的比较。
J Clin Invest. 1970 May;49(5):914-25. doi: 10.1172/JCI106311.
3
Haemoglobinopathies. The pathophysiology of beta-thalassaemia major.血红蛋白病。重型β地中海贫血的病理生理学。
J Clin Pathol Suppl (R Coll Pathol). 1974;8:12-8.
本文引用的文献
1
Jaundice in thalassemia minor: a consequence of "ineffective erythropoiesis".轻型地中海贫血中的黄疸：“无效红细胞生成”的结果。
N Engl J Med. 1962 Sep 13;267:523-9. doi: 10.1056/NEJM196209132671101.
2
HEREDITARY HEINZ-BODY ANAEMIA, THROMBOCYTOPENIA, AND HAEMOGLOBINOPATHY (HB KOELN) IN A GLASGOW FAMILY.格拉斯哥一个家族中的遗传性海因茨小体贫血、血小板减少症和血红蛋白病（血红蛋白科隆型）
Br Med J. 1964 Oct 31;2(5417):1099-103. doi: 10.1136/bmj.2.5417.1099.
3
HEREDITARY HEINZ-BODY ANAEMIA. A REPORT OF STUDIES ON FIVE PATIENTS WITH MILD ANAEMIA.遗传性 Heinz 小体贫血：5 例轻度贫血患者的研究报告
Br J Haematol. 1964 Jul;10:388-402. doi: 10.1111/j.1365-2141.1964.tb00715.x.
4
Hemoglobin metabolism in thalassemia. In vivo studies.
Am J Med. 1960 Jul;29:18-32. doi: 10.1016/0002-9343(60)90004-8.
5
Studies of the dipyrrylmethene ("fuscin") pigments. I. The anabolic significance of the fecal mesobilifuscin.二吡咯亚甲基（“褐菌素”）色素的研究。I. 粪便中胆褐素的合成代谢意义。
J Clin Invest. 1959 Jul;38(7):1166-74. doi: 10.1172/JCI103892.
6
Familial haemolytic anaemia with erythrocyte inclusion bodies, bilifuscinuria and abnormal haemoglobin (haemoglobin Galliera Genova).
Br J Haematol. 1965 Sep;11(5):511-7. doi: 10.1111/j.1365-2141.1965.tb00095.x.
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