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首页> 外文期刊>Thrombosis and Haemostasis: Journal of the International Society on Thrombosis and Haemostasis >Atypical haemolytic uraemic syndrome in a Japanese patient with DGKE genetic mutations

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Atypical haemolytic uraemic syndrome in a Japanese patient with DGKE genetic mutations

机译：一名患有DGKE基因突变的日本患者的非典型溶血性尿毒症综合征

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来源
《Thrombosis and Haemostasis: Journal of the International Society on Thrombosis and Haemostasis》 |2015年第4期|共2页
作者
Miyata Toshiyuki; Uchida Yumiko; Ohta Toshiyuki; Urayama Kohtaro; Yoshida Yoko; Fujimura Yoshihiro;
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正文语种 eng
中图分类心脏、血管（循环系）疾病;
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1. Atypical haemolytic uraemic syndrome in a Japanese patient with DGKE genetic mutations [J] . Miyata Toshiyuki, Uchida Yumiko, Ohta Toshiyuki, Thrombosis and Haemostasis: Journal of the International Society on Thrombosis and Haemostasis . 2015,第4期

机译：一名患有DGKE基因突变的日本患者的非典型溶血性尿毒症综合征
2. Posttransplant outcome of atypical haemolytic uraemic syndrome in a patient with thrombomodulin mutation: a case without recurrence [J] . Calogero Cirami, Enrico Eugenio Minetti, Leonardo Caroti, Clinical kidney journal. . 2015,第3期

机译：血栓调节蛋白突变患者的非典型溶血性尿毒症综合征的移植后预后：无复发病例
3. Posttransplant outcome of atypical haemolytic uraemic syndrome in a patient with thrombomodulin mutation: a case without recurrence [J] . Leonardo Caroti, Lorenzo Di Maria, Paolo Carta, Clinical kidney journal . 2015,第3期

机译：血栓调节蛋白突变患者的非典型溶血性综合征的后移植结果：一种没有复发的情况
4. The Spectrum of SCN5A Gene Mutations in Singapore Brugada Syndrome Patients [C] . Rita Yu Yin Yong, BY. Tan, LSH. Gan, International Molecular Medicine Tri-Conference. . 2016

机译：新加坡巴鲁达综合征患者SCN5A基因突变的谱
5. Evaluation of the accuracy of quantitative models in predicting Lynch syndrome (hereditary nonpolyposis colorectal cancer with defective DNA mismatch repair) mutations in a population-based sample of early-onset colorectal cancer patients [D] . Carpiniello, Lauren 2007

机译：在以人群为基础的早发性大肠癌患者样本中预测定量模型预测Lynch综合征（遗传性非息肉病性大肠直肠癌，DNA失配修复缺陷）的准确性
6. A patient with a homozygous diacylglycerol kinase epsilon (DGKE) gene mutation with atypical haemolytic uraemic syndrome and low C3 responded well to eculizumab: a case report [O] . Muneera Alabdulqader, Khalid Alfakeeh 2021

机译：患有纯合二氨基甘油激酶ε（DGKE）基因突变的患者具有非典型溶血性血糖综合征和低C3对Eculizumab作出良好的反应良好：案例报告
7. A patient with a homozygous diacylglycerol kinase epsilon (DGKE) gene mutation with atypical haemolytic uraemic syndrome and low C3 responded well to eculizumab: a case report [O] . Muneera Alabdulqader, Khalid Alfakeeh 2021

机译：患有纯合二氨基甘油激酶ε（DGKE）基因突变的患者，具有非典型溶血性血糖综合征和低C3对Eculizumab作出良好的反应良好：案例报告
8. JSC Exit Presentation: Effects of Genetics and Mutations on Acquired Long QT Syndrome. [R] . McFadden, R. 2014

机译：JsC退出演示：遗传和突变对获得性长QT综合征的影响。

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