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
相似文献
1
Dipyrrolic urinary pigments in congenital Heinz-body anaemia due to Hb köln and in thalassaemia.
Br Med J. 1966 Aug 13;2(5510):396. doi: 10.1136/bmj.2.5510.396.
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引用本文的文献
1
Congenital Heinz-body haemolytic anaemia due to haemoglobin Hammersmith.
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.
J Clin Invest. 1970 May;49(5):914-25. doi: 10.1172/JCI106311.
3
Haemoglobinopathies. The pathophysiology of beta-thalassaemia major.
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".
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.
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.
Br J Haematol. 1964 Jul;10:388-402. doi: 10.1111/j.1365-2141.1964.tb00715.x.
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Hemoglobin metabolism in thalassemia. In vivo studies.
Am J Med. 1960 Jul;29:18-32. doi: 10.1016/0002-9343(60)90004-8.
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Studies of the dipyrrylmethene ("fuscin") pigments. I. The anabolic significance of the fecal mesobilifuscin.
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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