Literature DB >> 6985793

Descriptive epidemiology of Creutzfeldt-Jakob disease in Chile.

S Galvez, C Masters, C Gajdusek.   

Abstract

Descriptive epidemiological data are presented from a survey of 35 cases of Creutzfeldt-Jakob disease (CJD) that occurred in Chile in the period 1955 to 1977. The average mortality in Chile (0.31 deaths per 1 million) and in urban Santiago (0.73 deaths per 1 million) is compared with data reported from other countries. An increasing incidence in recent years is probably related to a greater awareness of the disease. The familial occurrence of CJD in nine patients from five affected families is described, and its analysis suggests a genetically determined susceptibility with incubation periods of more than 30 years. Horizontal transmission of the disease may have occurred in one patient in whom the disease developed 13 years after the patient married into a family with seven other affected members.

Entities:  

Mesh:

Year:  1980        PMID: 6985793     DOI: 10.1001/archneur.1980.00500500041004

Source DB:  PubMed          Journal:  Arch Neurol        ISSN: 0003-9942


  16 in total

Review 1.  Bovine spongiform encephalopathy.

Authors:  W B Matthews
Journal:  BMJ       Date:  1990-02-17

2.  The nucleus basalis of Meynert in 20 definite cases of Creutzfeldt-Jakob disease.

Authors:  L Cartier; R Verdugo; C Vergara; S Galvez
Journal:  J Neurol Neurosurg Psychiatry       Date:  1989-03       Impact factor: 10.154

Review 3.  Epidemiological surveillance of Creutzfeldt-Jakob disease in the United Kingdom.

Authors:  R G Will
Journal:  Eur J Epidemiol       Date:  1991-09       Impact factor: 8.082

4.  Geographical distribution of cases of Creutzfeldt-Jakob disease in England and Wales 1970-84.

Authors:  S N Cousens; R Harries-Jones; R Knight; R G Will; P G Smith; W B Matthews
Journal:  J Neurol Neurosurg Psychiatry       Date:  1990-06       Impact factor: 10.154

5.  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

6.  Genetic prion disease: the EUROCJD experience.

Authors:  Gábor G Kovács; Maria Puopolo; Anna Ladogana; Maurizio Pocchiari; Herbert Budka; Cornelia van Duijn; Steven J Collins; Alison Boyd; Antonio Giulivi; Mike Coulthart; Nicole Delasnerie-Laupretre; Jean Philippe Brandel; Inga Zerr; Hans A Kretzschmar; Jesus de Pedro-Cuesta; Miguel Calero-Lara; Markus Glatzel; Adriano Aguzzi; Matthew Bishop; Richard Knight; Girma Belay; Robert Will; Eva Mitrova
Journal:  Hum Genet       Date:  2005-11-15       Impact factor: 4.132

7.  A retrospective study of Creutzfeldt-Jakob disease in England and Wales 1970-1979. II: Epidemiology.

Authors:  R G Will; W B Matthews; P G Smith; C Hudson
Journal:  J Neurol Neurosurg Psychiatry       Date:  1986-07       Impact factor: 10.154

8.  Ancestral origins and worldwide distribution of the PRNP 200K mutation causing familial Creutzfeldt-Jakob disease.

Authors:  H S Lee; N Sambuughin; L Cervenakova; J Chapman; M Pocchiari; S Litvak; H Y Qi; H Budka; T del Ser; H Furukawa; P Brown; D C Gajdusek; J C Long; A D Korczyn; L G Goldfarb
Journal:  Am J Hum Genet       Date:  1999-04       Impact factor: 11.025

9.  Creutzfeldt-Jakob disease in England and Wales, 1980-1984: a case-control study of potential risk factors.

Authors:  R Harries-Jones; R Knight; R G Will; S Cousens; P G Smith; W B Matthews
Journal:  J Neurol Neurosurg Psychiatry       Date:  1988-09       Impact factor: 10.154

10.  Subacute spongiform encephalopathy (Creutzfeldt-Jakob disease) associated with normal-pressure hydrocephalus Anatomoclinical report of one case.

Authors:  S Gálvez; S Ferrer; L Cartier; A Palma
Journal:  Acta Neurochir (Wien)       Date:  1980       Impact factor: 2.216

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