Literature DB >> 4620042

Letter: Creutzfeldt-Jakob disease: hypothesis for high incidence in Libyan Jews in Israel.

L Herzberg, B N Herzberg, C J Gibbs, W Sullivan, H Amyx, D C Gajdusek.   

Abstract

Mesh:

Year:  1974        PMID: 4620042     DOI: 10.1126/science.186.4166.848

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


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  11 in total

1.  Age and origin of the PRNP E200K mutation causing familial Creutzfeldt-Jacob disease in Libyan Jews.

Authors:  R Colombo
Journal:  Am J Hum Genet       Date:  2000-08       Impact factor: 11.025

Review 2.  Creutzfeldt-Jakob disease among Libyan Jews.

Authors:  A D Korczyn
Journal:  Eur J Epidemiol       Date:  1991-09       Impact factor: 8.082

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

Review 4.  The spongiform encephalopathies.

Authors:  R G Will
Journal:  J Neurol Neurosurg Psychiatry       Date:  1991-09       Impact factor: 10.154

5.  Complete penetrance of Creutzfeldt-Jakob disease in Libyan Jews carrying the E200K mutation in the prion protein gene.

Authors:  S Spudich; J A Mastrianni; M Wrensch; R Gabizon; Z Meiner; I Kahana; H Rosenmann; E Kahana; S B Prusiner
Journal:  Mol Med       Date:  1995-09       Impact factor: 6.354

6.  Papova virus-like particles in a nigral type of Creutzfeldt-Jakob disease.

Authors:  J de Reuck; W de Coster; G Otte; H vander Eecken
Journal:  J Neurol       Date:  1976       Impact factor: 4.849

Review 7.  Creutzfeldt--Jakob disease.

Authors:  W B Matthews
Journal:  Postgrad Med J       Date:  1978-09       Impact factor: 2.401

8.  Multiple sclerosis in the Orkney and Shetland Islands. II: The search for an exogenous aetiology.

Authors:  D C Poskanzer; J L Sheridan; L B Prenney; A M Walker
Journal:  J Epidemiol Community Health       Date:  1980-12       Impact factor: 3.710

9.  Clinical heterogeneity and unusual presentations of Creutzfeldt-Jakob disease in Jewish patients with the PRNP codon 200 mutation.

Authors:  J Chapman; P Brown; L G Goldfarb; A Arlazoroff; D C Gajdusek; A D Korczyn
Journal:  J Neurol Neurosurg Psychiatry       Date:  1993-10       Impact factor: 10.154

10.  Inherited prion disease (PrP lysine 200) in Britain: two case reports.

Authors:  J Collinge; M S Palmer; T Campbell; K C Sidle; D Carroll; A Harding
Journal:  BMJ       Date:  1993-01-30
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