Japans initiative on rare and undiagnosed diseases patients: To bring their diagnostic odyssey to an end, and beyond

Adachi T.; Imanishi N.; Umehara S.; Izumida Y.; Matsumoto N.; Kosaki K.; Matsubara Y.; Mizusawa H.; Suematsu M.

首页> 外文期刊>The Journal of investigative dermatology. >Japans initiative on rare and undiagnosed diseases patients: To bring their diagnostic odyssey to an end, and beyond

【24h】

Japans initiative on rare and undiagnosed diseases patients: To bring their diagnostic odyssey to an end, and beyond

机译：Japans倡议稀有和未诊断的疾病患者：将诊断奥德赛带到尽头，以外

获取原文

获取原文并翻译 | 示例

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
《The Journal of investigative dermatology.》 |2018年第19期|共1页
作者
Adachi T.; Imanishi N.; Umehara S.; Izumida Y.; Matsumoto N.; Kosaki K.; Matsubara Y.; Mizusawa H.; Suematsu M.;
展开▼
作者单位

Japan Agcy Med Res &

Dev AMED Tokyo Japan;

AMED Tokyo Japan;

AMED Tokyo Japan;

AMED Tokyo Japan;

Yokohama City Univ Grad Sch Med Yokohama Kanagawa Japan;

Keio Univ Sch Med Tokyo Japan;

Natl Ctr Child Hlth &

Dev Tokyo Japan;

Natl Ctr Neurol &

Psychiat Tokyo Japan;

AMED Tokyo Japan;

展开▼
收录信息
原文格式 PDF
正文语种 eng
中图分类皮肤病学与性病学;
关键词

相似文献

外文文献
中文文献
专利

1. Japans initiative on rare and undiagnosed diseases patients: To bring their diagnostic odyssey to an end, and beyond [J] . Adachi T., Imanishi N., Umehara S., The Journal of investigative dermatology. . 2018,第5a19期

机译：Japans倡议稀有和未诊断的疾病患者：将诊断奥德赛带到尽头，以外
2. 'Doctor google' ending the diagnostic odyssey in lysosomal storage disorders: Parents using internet search engines as an efficient diagnostic strategy in rare diseases [J] . BouwmanM.G., TeunissenQ.G.A., WijburgF.A., Archives of disease in childhood . 2010,第8期

机译：“谷歌医生”结束了溶酶体贮积病的诊断之旅：父母将互联网搜索引擎用作罕见疾病的有效诊断策略
3. ‘Doctor Google’ ending the diagnostic odyssey in lysosomal storage disorders: parents using internet search engines as an efficient diagnostic strategy in rare diseases [J] . Machtelt G Bouwman, Quirine G A Teunissen, Frits A Wijburg, Archives of disease in childhood . 2010,第8期

机译：“ Google医生”结束了溶酶体贮积病的诊断之旅：父母将互联网搜索引擎用作罕见疾病的有效诊断策略
4. Comprehensive Analysis of Patients with Undiagnosed Genetic Diseases Using the Patient Exploration Tools Suite (PETS) [C] . Elena Rojano, Pedro Seoane-Zonjic, Fernando M. Jabato, International work-conference on bioinformatics and biomedical engineering . 2020

机译：使用患者探索工具套件（PETS）对未确诊遗传病患者进行综合分析
5. Diagnostic Odyssey: Investigating the Role of a Mutation in the CUL4B Gene and its Effect on the CUL4B Protein Complex in a Patient with Seizures and Developmental Delay. [D] . Basila, Desiree. 2016

机译：诊断性奥德赛：研究癫痫发作和发育迟缓患者中CUL4B基因突变的作用及其对CUL4B蛋白复合物的影响。
6. Japan’s initiative on rare and undiagnosed diseases (IRUD): towards an end to the diagnostic odyssey [O] . Takeya Adachi, Kazuo Kawamura, Yoshihiko Furusawa, 2017

机译：日本针对罕见和未确诊疾病的倡议（IRUD）：终结诊断性旅程
7. 744 Japans initiative on rare and undiagnosed diseases patients: To bring their diagnostic odyssey to an end, and beyond [O] . T. Adachi, N. Imanishi, S. Umehara, 2018

机译：744岁的日本初始疾病患者倡议：将诊断奥德赛带到尽头，超越

Japans initiative on rare and undiagnosed diseases patients: To bring their diagnostic odyssey to an end, and beyond

著录项

相似文献

相关主题

期刊订阅