Prion diseases reported in the “Annual of the Pathological Autopsy Cases in Japan”

Author:

Horimoto Yoshihiko,Sato Chikako,Inagaki Aki,Tajima Toshihisa,Hibino Hiroaki,Kabasawa Hidehiro,Inagaki Hiroshi

Publisher

Elsevier BV

Subject

Clinical Neurology,Neurology

Reference23 articles.

1. Creutzfeldt-Jakob disease in Austria: an autopsy-controlled study;Gelpi;Neuroepidemiology,2008

2. Accuracy of diagnosis criteria in patients with suspected diagnosis of sporadic Creutzfeldt-Jakob disease and detection of 14–3-3 protein, France, 1992 to 2009;Peckeu;Euro Surveill,2017

3. Brett F. CJD surveillance in the Republic of Ireland from 2005 to 2015: a suggested algorithm for referrals;Loftus;Clin. Neuropathol.,2017

4. Mizusawa H. The annual report of the research committee on surveillance and infection control of prion disease in FY2019, summary/shared research report. Researches on rare and intractable diseases. Health, Labour and Welfare Policy Research Grants. The Ministry of Health, Labour and Welfare, Japan. http://prion.umin.jp/survey/.

5. Creutzfeldt-Jakob disease surveillance in Australia: update to 31 December 2018;Stehmann;Commun Dis Intell (2018).,2019

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