[不稳定血红蛋白维也纳的特性] - Suppr

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[Properties of the unstable Hb Wien].

作者信息

Kleihauer E, Betke K

出版信息

Klin Wochenschr. 1972 Oct 1;50(19):907-9. doi: 10.1007/BF01487920.

DOI:10.1007/BF01487920

PMID:5081733

Abstract

摘要

相似文献

[Properties of the unstable Hb Wien].[不稳定血红蛋白维也纳的特性]

Klin Wochenschr. 1972 Oct 1;50(19):907-9. doi: 10.1007/BF01487920.

Laboratory approach to diagnosis of hemoglobin abnormalities.

Clin Obstet Gynecol. 1969 Mar;12(1):76-114. doi: 10.1097/00003081-196903000-00004.

Hemoglobin S-Ga Georgia disease: a case report.血红蛋白S-佐治亚病：一例报告

Acta Haematol. 1974;51(5):315-20. doi: 10.1159/000208312.

[Electron microscopic examinations of erythrocytes in hemoglobinopathy (Hb Wien)].[血红蛋白病（维也纳血红蛋白，Hb Wien）中红细胞的电子显微镜检查]

Wien Z Inn Med. 1972;53(11):580-5.

Chemical heterogeneity of fetal hemoglobin in subjects with sickle cell anemia, homozygous Hb-C disease, SC disease, and various combinations of hemoglobin variants.镰状细胞贫血、纯合子血红蛋白C病、血红蛋白SC病以及各种血红蛋白变异体组合的患者中胎儿血红蛋白的化学异质性。

Clin Chim Acta. 1972 Apr;38(1):5-16. doi: 10.1016/0009-8981(72)90201-x.

[A2' (B2) hemoglobin associated with beta thalassemia and hereditary persistence of fetal hemoglobin. Study in 3 Colombian families].与β地中海贫血和胎儿血红蛋白遗传性持续存在相关的[A2'（B2）血红蛋白。对3个哥伦比亚家庭的研究]

Sangre (Barc). 1973;18(2):145-56.

Hemoglobin SO Arabia disease in a black American.

Am J Med Sci. 1973 Apr;265(4):266-74. doi: 10.1097/00000441-197304000-00001.

[Unusual pathological hemoglobins: Hb unstable, hemoglobins with altered oxygen affinity and Hb M].[异常病理性血红蛋白：不稳定血红蛋白、氧亲和力改变的血红蛋白及血红蛋白M]

Recenti Prog Med. 1974 Nov;57(5):415-68.

High resolution analysis of hemoglobins: polyacrylamide isoelectric focusing.血红蛋白的高分辨率分析：聚丙烯酰胺等电聚焦

Biochem Med. 1972 Dec;6(6):553-60. doi: 10.1016/0006-2944(72)90010-5.

Hemoglobin Köln in a black: pre- and post-splenectomy red cell survival (DF32P and 51Cr) and the pathogenesis of hemoglobin instability.黑色的科隆血红蛋白：脾切除术前和术后红细胞存活情况（DF32P和51Cr）以及血红蛋白不稳定性的发病机制。

Blood. 1973 Nov;42(5):771-81.

引用本文的文献

Hemolytic anemia due to the unstable hemoglobin Wien: manifestations and long-term course in the largest pedigree identified to date.因不稳定血红蛋白维也纳型导致的溶血性贫血：迄今发现的最大谱系中的临床表现及长期病程

Haematologica. 2020 May;105(5):e253-e255. doi: 10.3324/haematol.2019.236562. Epub 2020 Feb 6.

本文引用的文献

[CONGENITAL HEMOLYTIC ANEMIA WITH MESOBILIFUSCINURIA AND INCLUSION BODY FORMATION AFTER SPLENECTOMY].[先天性溶血性贫血伴中胆色素质尿症及脾切除术后包涵体形成]

Acta Haematol. 1964 Nov;32:314-20. doi: 10.1159/000209576.

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.

Estimation of small percentages of foetal haemoglobin.微量胎儿血红蛋白的测定。

Nature. 1959 Dec 12;184(Suppl 24):1877-8. doi: 10.1038/1841877a0.

[Heat lability and acid stability of hemoglobin H].[血红蛋白H的热不稳定性和酸稳定性]

Klin Wochenschr. 1960 Jun 1;38:529-32. doi: 10.1007/BF01482681.

[Hemoglobin Zuerich: a new hemoglobin anomaly with sulfonamide-induced inclusion body anemia].

Helv Paediatr Acta. 1960 Dec;15:499-514.

[Fetal and residual hemoglobin in the erythrocytes and erythroblasts of human fetuses and newborn infants].[人类胎儿和新生儿红细胞及成红细胞中的胎儿血红蛋白和残余血红蛋白]

Blut. 1958 Nov;4(5):241-9. doi: 10.1007/BF01630321.

[Demonstration of fetal hemoglobin in erythrocytes of a blood smear].[血涂片红细胞中胎儿血红蛋白的显示]

Klin Wochenschr. 1957 Jun 15;35(12):637-8. doi: 10.1007/BF01481043.

[Familial hemolytic anemia with Heinz body formation after splenectomy and mesobilifuscin in urine with abnormal hemoglobin].

Dtsch Med Wochenschr. 1967 Jan 20;92(3):98-104. doi: 10.1055/s-0028-1103580.

Hemoglobin Freiburg: abnormal hemoglobin due to deletion of a single amino acid residue.弗赖堡血红蛋白：因单个氨基酸残基缺失导致的异常血红蛋白。

Science. 1966 Nov 25;154(3752):1024-7. doi: 10.1126/science.154.3752.1024.

Hemoglobin sabine beta 91 (F 7) leu → pro. An unstable variant causing severe anemia with inclusion bodies.血红蛋白萨宾β91（F7）亮氨酸→脯氨酸。一种导致严重贫血并伴有包涵体的不稳定变体。

N Engl J Med. 1969 Apr 3;280(14):739-45. doi: 10.1056/NEJM196904032801402.

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