Author:
Yamada Masahito,Nozaki Ichiro,Hamaguchi Tsuyoshi,Noguchi-Shinohara Moeko,Kitamoto Tetsuyuki,Nakamura Yosikazu,Sato Takeshi,Mizusawa Hidehiro
Publisher
Societas Neurologica Japonica
Reference10 articles.
1. Clinical diagnosis of MM2-type sporadic Creutzfeldt-Jakob disease
2. Genetic prion disease: the EUROCJD experience
3. Clinical features and diagnosis of dura mater graft-associated Creutzfeldt-Jakob disease
4. Cross-sequence Transmission of Sporadic Creutzfeldt-Jakob Disease Creates a New Prion Strain
5. 5) World Health Organization: The revision of the surveillance case definition for variant Creutzfeldt-Jakob Disease (vCJD). Report of a WHO consultation Edinburgh, United Kingdom 17 May 2001 (available at http://www.who.int/csr/resources/publications/bse/en/whocdscsreph20015.pdf)
Cited by
3 articles.
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