Co-Existence of Hereditary Pyrimidine 5’-Nucleotidase Deficiency and Heterozygous α-Thalassemia: A Case Presentation

A. Agapidou; S. Theodoridou; K. Tegos; E. Mandala; E. Leukou; O. Karakasidou; B. Aletra; A. Sevastidou; M. Alemayehou; E. Voskaridou

首页> 外文期刊>Turkish Journal of Hematology >Co-Existence of Hereditary Pyrimidine 5’-Nucleotidase Deficiency and Heterozygous α-Thalassemia: A Case Presentation

【24h】

Co-Existence of Hereditary Pyrimidine 5’-Nucleotidase Deficiency and Heterozygous α-Thalassemia: A Case Presentation

机译：遗传性嘧啶5'-核苷酸酶缺乏症与杂合子α-地中海贫血并存：一例

获取原文

掌桥外文数据库（机构版） >>

开具论文收录证明 >>

文献代查 >>

页面导航

著录项
相似文献
相关主题

著录项

来源
《Turkish Journal of Hematology》 |2012年第4期|共3页
作者
A. Agapidou; S. Theodoridou; K. Tegos; E. Mandala; E. Leukou; O. Karakasidou; B. Aletra; A. Sevastidou; M. Alemayehou; E. Voskaridou;
展开▼
作者单位

展开▼
收录信息
原文格式 PDF
正文语种
中图分类血液及淋巴系疾病;
关键词

相似文献

外文文献
中文文献
专利

1. Hereditary erythrocyte pyrimidine 5'-nucleotidase deficiency: a biochemical, genetic and clinical overview. [J] . Chiarelli LR, Fermo E, Zanella A, Hematology. . 2006,第1期

机译：遗传性红细胞嘧啶5'-核苷酸酶缺乏症：生化，遗传和临床概述。
2. Pyrimidine-5 '-nucleotidase Campinas, a new mutation (p.R56G) in the NT5C3 gene associated with pyrimidine-5 '-nucleotidase type I deficiency and influence of Gilbert's Syndrome on clinical expression [J] . dos Santos Andrey, Cordeiro Dantas Larissa Elizabeth, Traina Fabiola, Blood cells, molecules and diseases . 2014,第4期

机译：嘧啶5'-核苷酸酶Campinas，与嘧啶5'-核苷酸酶I型缺乏相关的NT5C3基因新突变（p.R56G）和吉尔伯特综合征对临床表达的影响
3. New missense homozygous mutation (Q270Ter) in the pyrimidine 5′ nucleotidase type I-related gene in two Indian families with hereditary non-spherocytic hemolytic anemia [J] . WarangP., KedarP., KarR., Annals of hematology . 2013,第5期

机译：印度两个遗传性非球囊性溶血性贫血家庭的嘧啶5'核苷酸酶I型相关基因中的新的错义纯合突变（Q270Ter）
4. Pseudo-Homozygous APC Resistance Due to Coinheritance of Heterozygous Factor V - R506Q and Type I Deficiency Associated with Thrombosis [C] . A. Pavlova, R. Loreth, D. Delev, Hemophilia Symposium . 2008

机译：由于杂合因子V - R506Q的辅导引起的假纯合的APC抗性，I型血栓形成相关的I型缺陷
5. Parameterization and Concise Representation in Graph Algorithms: Leaf Powers, Subgraphs with Hereditary Properties, and Activity-on-Edge Minimization [D] . Havvaei, Elham. 2021

机译：图算法中的参数化和简洁表示：叶子力，具有遗传性质的子图，以及偏见的活动最小化
6. Co-Existence of Hereditary Pyrimidine 5’-Nucleotidase Deficiency and Heterozygous α-Thalassemia: A Case Presentation [O] . A. Agapidou, S. Theodoridou, K. Tegos, 2012

机译：遗传性嘧啶5-核苷酸酶缺乏症与杂合子α-地中海贫血并存：一例
7. Co-Existence of Hereditary Pyrimidine 5’-Nucleotidase Deficiency and Heterozygous α-Thalassemia: A Case Presentation [O] . A. Agapidou, S. Theodoridou, K. Tegos, 2012

机译：遗传性嘧啶5'-核苷酸酶缺乏症和杂合子α-地中海贫血的共存：病例报告

Co-Existence of Hereditary Pyrimidine 5’-Nucleotidase Deficiency and Heterozygous α-Thalassemia: A Case Presentation

著录项

相似文献

相关主题

期刊订阅