DOI
stands for Digital Object Identifier
(
D
igital
O
bject
I
dentifier
)
,
and is the unique identifier for objects on the internet. It can be used to create persistent link and to cite articles.
Using DOI as a persistent link
To create a persistent link, add「http://dx.doi.org/」
「
http://dx.doi.org/
」
before a DOI.
For instance, if the DOI of an article is
10.5297/ser.1201.002
, you can link persistently to the article by entering the following link in your browser:
http://dx.doi.org/
10.5297/ser.1201.002
。
The DOI link will always direct you to the most updated article page no matter how the publisher changes the document's position, avoiding errors when engaging in important research.
Cite a document with DOI
When citing references, you should also cite the DOI if the article has one. If your citation guideline does not include DOIs, you may cite the DOI link.
DOIs allow accurate citations, improve academic contents connections, and allow users to gain better experience across different platforms. Currently, there are more than 70 million DOIs registered for academic contents. If you want to understand more about DOI, please visit airiti DOI Registration ( doi.airiti.com ) 。
Epidemiology and Risk Factor for Creutzfeldt-Jakob Disease in Taiwan
柯海韻 , Masters Advisor:黃璉華
繁體中文
DOI:
10.6342/NTU.2012.02518
庫賈氏病 ; 流行病學 ; 危險因子 ; Creutzfeldt-Jakob disease ; Epidemiology ; Risk Factor


- Alper, T., & Cramp, W. (1967). Does the agent of scrapie replicate without nucleic acid? Nature, 214, 764-766.
連結: - Brow, D. R. (2005). Neurodegeneration and Prion Disease Boston: Springer Science+Business Media, Inc.
連結: - Chi, N. F., Lee, Y. C., Lu, Y. C., Wu, H. M., & Soong, B. W. (2010). Transmissible spongiform encephalopathies with P102L mutation of PRNP manifesting different phenotypes: clinical, neuroimaging, and electrophysiological studies in Chinese kindred in Taiwan. Journal of Neurology, 257(2), 191-197.
連結: - Davanipour, Z., Hofman, A., Kondo, K., Matthews, W., Will, R., & Duijn, C. (1996). Risk factors for Creutzfeldt-Jakob disease: a reanalysis of case-control studies.
連結: - Gabizon, R., Telling, G., Meiner, Z., Halimi, M., Kahana, I., & Prusiner, S. B. (1996). Insoluble wild-type and protease resistant mutant prion protein in brains of patients with inherited prion disease. Nature medicine, 2(1), 59-64.
連結: