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。 - Suppr

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超能文献

Congenital Heinz-body haemolytic anaemia due to haemoglobin Hammersmith.

作者信息

Shinton N K, Williams H P, Thursby-Pelham D C

出版信息

Postgrad Med J. 1969 Sep;45(527):629-32. doi: 10.1136/pgmj.45.527.629.

DOI:10.1136/pgmj.45.527.629

PMID:5809559

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2466132/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/472c/2466132/4db138e33a36/postmedj00369-0058-a.jpg

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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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A Swedish family with haemolytic anaemia, Heinz bodies and an abnormal haemoglobin.

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Haemoglobin Hammersmith (beta-42 (CDI) Phe replaced by ser).

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引用本文的文献

Haemoglobin Hammersmith precludes monitoring with conventional pulse oximetry.血红蛋白汉默史密斯型妨碍使用传统脉搏血氧饱和度仪进行监测。

Can J Anaesth. 1994 Oct;41(10):965-8. doi: 10.1007/BF03010939.

Hemoglobin Louisville (beta-42 (CD1) phe-leu): an unstable variant causing mild hemolytic anemia.

J Clin Invest. 1971 Nov;50(11):2395-402. doi: 10.1172/JCI106738.

本文引用的文献

Symposium: Hæmolytic Anæmias.专题研讨会：溶血性贫血

Proc R Soc Med. 1965 Jul;58(7):514-6. doi: 10.1177/003591576505800718.

Heinz body phenomenon in erythrocytes; a review.

Blood. 1949 May;4(5):479-97.

Congenital hemolytic disease associated with red cell inclusion bodies, abnormal pigment metabolism and an electrophoretic hemoglobin abnormality.与红细胞包涵体、异常色素代谢及血红蛋白电泳异常相关的先天性溶血性疾病。

Blood. 1960 Sep;16:1239-52.

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.

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.

Br J Haematol. 1964 Jul;10:281-90. doi: 10.1111/j.1365-2141.1964.tb00704.x.

HEMOLYTIC DISEASE ASSOCIATED WITH THE PRODUCTION OF ABNORMAL HEMOGLOBIN AND INTRAERYTHROCYTIC HEINZ BODIES.与异常血红蛋白产生及红细胞内海因茨小体相关的溶血性疾病。

Nihon Ketsueki Gakkai Zasshi. 1963 Apr;26:164-73.

Hemoglobin Zurich. I. A new hemoglobin anomaly associated with acute hemolytic episodes with inclusion bodies after sulfonamide therapy.苏黎世血红蛋白。I. 一种与磺胺类药物治疗后伴有包涵体的急性溶血发作相关的新型血红蛋白异常。

Blood. 1962 Sep;20:261-71.

Metabolic abnormalities of erythrocytes from patients with congenital nonspherocytic hemolytic anemia.先天性非球形红细胞溶血性贫血患者红细胞的代谢异常。

J Pediatr. 1959 Sep;55:319-36. doi: 10.1016/s0022-3476(59)80228-6.

Oxidative hemolysis and precipitation of hemoglobin. I. Heinz body anemias as an acceleration of red cell aging.氧化溶血与血红蛋白沉淀。I. 海因茨小体贫血作为红细胞衰老的加速过程。

J Clin Invest. 1960 Dec;39(12):1818-36. doi: 10.1172/JCI104206.

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