• 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

[Pyruvate kinase deficiency hereditary hemolytic anemia (author's transl)].

作者信息

Labar B, Stanulović M, Jerence D

出版信息

Lijec Vjesn. 1979 Sep;101(9):557-9.

PMID:542089
Abstract
摘要

相似文献

1
[Pyruvate kinase deficiency hereditary hemolytic anemia (author's transl)].丙酮酸激酶缺乏遗传性溶血性贫血(作者译)
Lijec Vjesn. 1979 Sep;101(9):557-9.
2
[Oxygenation curves in enzymopathic hemolytic anemias].[酶病性溶血性贫血中的氧合曲线]
Acta Univ Palacki Olomuc Fac Med. 1984;106:123-31.
3
[Glucose-6-phosphate dehydrogenase deficiency hereditary hemolytic anemia (author's transl)].葡萄糖-6-磷酸脱氢酶缺乏症遗传性溶血性贫血(作者译)
Lijec Vjesn. 1979 Sep;101(9):560-2.
4
Pyruvate kinase deficiency anemia with terminal myelofibrosis and osteosclerosis in a beagle.一只比格犬患有丙酮酸激酶缺乏性贫血并伴有终末期骨髓纤维化和骨硬化
J Am Vet Med Assoc. 1975 Jun 15;166(12):1170-5.
5
[Hemochromatosis and puryvate kinase deficiency (author's transl)].血色素沉着症与丙酮酸激酶缺乏症(作者译)
Ann Med Interne (Paris). 1979 Dec;130(12):679-83.
6
A case of congenital red cell pyruvate kinase deficiency associated with hereditary stomatocytosis.一例与遗传性口形红细胞增多症相关的先天性红细胞丙酮酸激酶缺乏症
Blood Cells Mol Dis. 2008 Nov-Dec;41(3):261-2. doi: 10.1016/j.bcmd.2008.07.001. Epub 2008 Aug 16.
7
Erythrocyte pyruvate kinase deficiency. The influence of physiologically important metabolites on the function of normal and defective enzymes.红细胞丙酮酸激酶缺乏症。生理上重要的代谢物对正常和缺陷酶功能的影响。
Enzyme Protein. 1994;48(3):149-63.
8
[Erythroenzymopathies in Japan (author's transl)].日本的红细胞酶病(作者译)
Rinsho Ketsueki. 1979 Jul;20(7):718-23.
9
[Haemolytic anaemia due to hereditary defect of erythrocyte pyruvate kinase. Clinical, familial, and biological study of ten cases (author's transl)].[红细胞丙酮酸激酶遗传性缺陷所致溶血性贫血。10例临床、家族及生物学研究(作者译)]
Sangre (Barc). 1980;25(1):51-62.
10
[Erythrocyte metabolism in patients with acute leukemia and a deficiency of the enzyme pyruvate kinase].[急性白血病合并丙酮酸激酶缺乏患者的红细胞代谢]
Lijec Vjesn. 1984 Nov-Dec;106(11-12):447-51.