Prion diseases with a focus on Creutzfeldt-Jakob disease, a summary of the incidence of Creutzfeldt-Jakob disease in the Czech Republic over the last 17 years, 2000-2017

Kolarova K.; Maresova M.; Mandakova Z.; Kyncl J.

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Prion diseases with a focus on Creutzfeldt-Jakob disease, a summary of the incidence of Creutzfeldt-Jakob disease in the Czech Republic over the last 17 years, 2000-2017

机译：朊病毒疾病专注于Creutzfeldt-Jakob疾病，在过去17年来，2000-2017的捷克共和国在捷克共和国的发病率摘要

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Background: Creutzfeldt-Jakob disease (CJD) is a prion disease. It is a rare, rapidly progressing fatal disorder of the central nervous system, which occurs in four forms: sporadic (sCJD), genetic/familial (gCJD), iatrogenic (iCJD), and variant (vCJD).

机译：背景：Creutzfeldt-Jakob疾病（CJD）是一种朊病毒疾病。它是一种罕见的，快速进展的中枢神经系统的致命障碍，它以四种形式发生：散发性（SCJD），遗传/家族性（GCJD），认可（ICJD）和变体（VCJD）。

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《Fortschritte der Physik》 |2018年第4期|共6页
作者
Kolarova K.; Maresova M.; Mandakova Z.; Kyncl J.;
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作者单位

Statni Zdravotni Ustav Oddeleni Epidemiol Infekcnich Nemoci Ctr Epidemiol &

Mikrobiol Prague Czech Republic;

Protiepidemicke Oddeleni Hyg Stanice Hlavniho Mes Pobocky Praha Jih Prague Czech Republic;

Statni Zdravotni Ustav Oddeleni Epidemiol Infekcnich Nemoci Ctr Epidemiol &

Mikrobiol Prague Czech Republic;

Statni Zdravotni Ustav Oddeleni Epidemiol Infekcnich Nemoci Ctr Epidemiol &

Mikrobiol Prague Czech Republic;

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原文格式 PDF
正文语种 cze
中图分类物理学;
关键词
Creutzfeldt-Jakob disease; epidemiology; sporadic CDJ; familial CDJ; iatrogenic CDJ; variant CDJ; prion;

机译：Creutzfeldt-Jakob疾病;流行病学;零星CDJ;家族性CDJ;认识CDJ;变体CDJ;朊病毒;

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1. Prion diseases with a focus on Creutzfeldt-Jakob disease, a summary of the incidence of Creutzfeldt-Jakob disease in the Czech Republic over the last 17 years, 2000-2017 [J] . Kolarova K., Maresova M., Mandakova Z., Fortschritte der Physik . 2018,第4期

机译：朊病毒疾病专注于Creutzfeldt-Jakob疾病，在过去17年来，2000-2017的捷克共和国在捷克共和国的发病率摘要
2. Creutzfeldt-Jakob disease in a patient with an R208H mutation of the prion protein gene (PRNP) and a 17-kDa prion protein fragment [J] . Sigrun Roeber, Bjarne Krebs, Manuela Neumann, Acta Neuropathologica . 2005,第4期

机译：患有ut病毒蛋白基因（PRNP）的R208H突变和17-kDa pr病毒蛋白片段的患者患有Creutzfeldt-Jakob病
3. Cost-effectiveness of prion filtration of red blood cells to reduce the risk of transfusion-transmitted variant Creutzfeldt-Jakob disease in the Republic of Ireland [J] . TeljeurC., FlatteryM., HarringtonP., Transfusion: The Journal of the American Association of Blood Banks . 2012,第11期

机译：在爱尔兰共和国进行红细胞病毒过滤以降低输血传播的变异型克雅氏病风险的成本效益
4. Three-Dimensional Reconstruction of the Florid Plaque in variant Creutzfeldt-Jakob Diseases [C] . M. Zubert, M. Napieralska, A. Napieralski, Nano Science and Technology Institute(NSTI) Nanotechnology Conference and Trade Show(NSTI Nanotech 2006) vol.2 . 2006

机译：变种克雅氏病中的小斑块的三维重建
5. Imputation based methods for incidence rate estimation of rare diseases from federal and state mortality data supplemented with disease registry data [D] . Jalal, Kabir 2015

机译：基于归因法的联邦和州死亡率数据与疾病登记数据相结合的罕见病发病率估算方法
6. A case-control study of sporadic Creutzfeldt-Jakob disease in Switzerland: analysis of potential risk factors with regard to an increased CJD incidence in the years 2001–2004 [O] . Jessica Ruegger, Katharina Stoeck, Lorenz Amsler, 2009

机译：瑞士散发性克雅氏病的病例对照研究：2001-2004年期间增加的克雅氏病发病率的潜在危险因素分析
7. A case-control study of sporadic Creutzfeldt-Jakob disease in Switzerland: analysis of potential risk factors with regard to an increased CJD incidence in the years 2001–2004 [O] . 2009

机译：瑞士散发性克雅氏病的病例对照研究：2001-2004年期间增加的克雅氏病发病率的潜在危险因素分析
8. Informational Issue Summary: FDA's Currently-Recommended Policies to Reduce the Possible Risk of Transmission of Creutzfeldt-Jakob Disease (CJD) and Variant Creutzfeldt-Jakob Disease (vCJD) by Blood and Blood Products [R] . 2010

机译：信息问题摘要：FDa目前推荐的政策旨在通过血液和血液制品减少克罗伊茨费尔特 - 雅各布病（CJD）和变异克雅氏病（vCJD）传播的可能风险

Prion diseases with a focus on Creutzfeldt-Jakob disease, a summary of the incidence of Creutzfeldt-Jakob disease in the Czech Republic over the last 17 years, 2000-2017

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