• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

[Clinicohematologic effects of hemoglobin Altdorf (alpha 2 beta 2 135 Ala replaced by Pro)].

作者信息

Marti H R, Scherrer R, Piller M

出版信息

Folia Haematol Int Mag Klin Morphol Blutforsch. 1980;107(4):648-53.

PMID:6162732
Abstract

Hb Altdorf alpha 2 beta 2 135 Ala leads to Pro is an unstable variant occurring near Lecce in Italy. The abnormal hemoglobin does not separate from Hb A in the electrophoresis. In vitro a marked Heinz body formation is produced with phenylhydrazin. In heterozygous individuals an almost compensated hemolysis and a slight splenomegaly are found. Hemolysis can be aggravated by exogenous factors. A rather severe hemolysis was induced by a viral infection in a 3 years old girl.

摘要

相似文献

1
[Clinicohematologic effects of hemoglobin Altdorf (alpha 2 beta 2 135 Ala replaced by Pro)].
Folia Haematol Int Mag Klin Morphol Blutforsch. 1980;107(4):648-53.
2
[Structural variants in hemoglobin occurring in the Czech Republic].
Vnitr Lek. 1995 Jan;41(1):13-20.
3
[New anomalous structural hemoglobin variant: hemoglobin Dagestan (alpha 60 Lys replaced by Glu)].[新型异常结构血红蛋白变体:达吉斯坦血红蛋白(α60位赖氨酸被谷氨酸取代)]
Probl Gematol Pereliv Krovi. 1981 Dec;26(12):3-6.
4
Observations on the rate and mechanism of hemolysis in individuals with Hb Zürich [His E7(63)beta leads to Arg]: II. Thermal denaturation of hemoglobin as a cause of anemia during fever.对携带苏黎世血红蛋白[组氨酸E7(63)β突变为精氨酸]个体的溶血速率及机制的观察:II. 发热期间血红蛋白热变性作为贫血的一个原因
Johns Hopkins Med J. 1979 Apr;144(4):109-16.
5
Hemoglobin Tochigi disease, a new unstable hemoglobin hemolytic anemia found in a Japanese family.血红蛋白栃木病,一种在日本家庭中发现的新型不稳定血红蛋白溶血性贫血。
Nihon Ketsueki Gakkai Zasshi. 1971 Aug;34(4):484-97.
6
Hb Montreal II: a novel elongated beta-globin variant caused by a frameshift mutation [beta142 (-C)].血红蛋白蒙特利尔II:一种由移码突变[β142(-C)]引起的新型延长型β珠蛋白变体。
Hemoglobin. 2008;32(4):351-9. doi: 10.1080/03630260802173593.
7
[Hemoglobin D Punjab. Apropos of 2 families].[血红蛋白D旁遮普型。关于两个家族]
Schweiz Med Wochenschr. 1979 Aug 25;109(32):1187-93.
8
[Hemoglobin G Coushatta (beta 22 (B4) glu leads to ala) in Algeria: an homozygous case].
Nouv Rev Fr Hematol (1978). 1979;21(3):225-30.
9
Distinct phenotypic expression associated with a new hyperunstable alpha globin variant (Hb heraklion, alpha1cd37(C2)Pro>0): comparison to other alpha-thalassemic hemoglobinopathies.与一种新的高度不稳定α珠蛋白变体(Hb 伊拉克利翁,α1cd37(C2)Pro>0)相关的独特表型表达:与其他α地中海贫血血红蛋白病的比较。
Blood Cells Mol Dis. 2000 Aug;26(4):276-84. doi: 10.1006/bcmd.2000.0307.
10
[Hemoglobin Sydney--alpha beta 2 67 (E11) Val-Ala and hemoglobin Olomouc alpha 2 beta 2 86 (F 2) Ala-Asp in Czech families. DNA sequence analysis for a more accurate diagnosis of hemoglobinopathies].
Vnitr Lek. 1998 Jun;44(6):347-9.