Literature DB >> 6355897

Creutzfeldt-Jakob disease in Japan.

S Tsuji, Y Kuroiwa.   

Abstract

In a nationwide survey of Creutzfeldt-Jakob disease (CJD) in Japan, the point prevalence rate on June 1, 1978 in Fukuoka Prefecture and the estimated national prevalence rate were approximately one per one million population. The minimal period prevalence rate was 0.45 per one million population. The minimal annual incidence and the minimal annual mortality rate were 0.19 and 0.15 per one million population, respectively. The geographic distribution of CJD in Japan was uniform. Clinically, CJD affected the central nervous system diffusely and was rapidly fatal. No specific features were found in family, social, and past histories.

Entities:  

Mesh:

Year:  1983        PMID: 6355897     DOI: 10.1212/wnl.33.11.1503

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  12 in total

1.  Incidence of Creutzfeldt-Jakob disease in Taiwan: a prospective 10-year surveillance.

Authors:  Chien-Jung Lu; Yu Sun; Shun-Sheng Chen
Journal:  Eur J Epidemiol       Date:  2010-03-24       Impact factor: 8.082

2.  Geographic difference of mortality of Creutzfeldt-Jakob disease in Japan.

Authors:  Yosikazu Nakamura; Makoto Watanabe; Kiwamu Nagoshi; Masahito Yamada; Hidehiro Mizusawa
Journal:  J Epidemiol       Date:  2007-01       Impact factor: 3.211

3.  A retrospective study of Creutzfeldt-Jakob disease in Italy (1972-1986).

Authors:  C Masullo; M Pocchiari; G Neri; P Casaccia; A Iavarone; A Ladogana; G Macchi
Journal:  Eur J Epidemiol       Date:  1988-12       Impact factor: 8.082

4.  Differential diagnosis of Jakob-Creutzfeldt disease.

Authors:  Ross W Paterson; Charles C Torres-Chae; Amy L Kuo; Tim Ando; Elizabeth A Nguyen; Katherine Wong; Stephen J DeArmond; Aissa Haman; Paul Garcia; David Y Johnson; Bruce L Miller; Michael D Geschwind
Journal:  Arch Neurol       Date:  2012-12

5.  Creutzfeldt-Jakob disease presenting as progressive aphasia.

Authors:  E C Shuttleworth; A J Yates; J D Paltan-Ortiz
Journal:  J Natl Med Assoc       Date:  1985-08       Impact factor: 1.798

Review 6.  A clinicopathological approach to the diagnosis of dementia.

Authors:  Fanny M Elahi; Bruce L Miller
Journal:  Nat Rev Neurol       Date:  2017-07-14       Impact factor: 42.937

7.  Polymorphisms of the prion protein gene in Italian patients with Creutzfeldt-Jakob disease.

Authors:  M Salvatore; M Genuardi; R Petraroli; C Masullo; M D'Alessandro; M Pocchiari
Journal:  Hum Genet       Date:  1994-10       Impact factor: 4.132

8.  Immunohistochemical confirmation of Creutzfeldt-Jakob disease with a long clinical course with amyloid plaque core antibodies.

Authors:  T Kitamoto; J Tateishi
Journal:  Am J Pathol       Date:  1988-06       Impact factor: 4.307

Review 9.  Prion Diseases.

Authors:  Michael D Geschwind
Journal:  Continuum (Minneap Minn)       Date:  2015-12

10.  Epidemiologic implications of Creutzfeldt-Jakob disease in a 19 year-old girl.

Authors:  P Brown; F Cathala; R Labauge; M Pages; J C Alary; H Baron
Journal:  Eur J Epidemiol       Date:  1985-03       Impact factor: 8.082

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