Genetic prion disease: the EUROCJD experience-Reference-Cited by-同舟云学术

Genetic prion disease: the EUROCJD experience

Published:2005-09-27 Issue:2 Volume:118 Page:166-174
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Kovács Gábor G.,Puopolo Maria,Ladogana Anna,Pocchiari Maurizio,Budka Herbert,van Duijn Cornelia,Collins Steven J.,Boyd Alison,Giulivi Antonio,Coulthart Mike,Delasnerie-Laupretre Nicole,Brandel Jean Philippe,Zerr Inga,Kretzschmar Hans A.,de Pedro-Cuesta Jesus,Calero-Lara Miguel,Glatzel Markus,Aguzzi Adriano,Bishop Matthew,Knight Richard,Belay Girma,Will Robert,Mitrova Eva

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s00439-005-0020-1.pdf

Reference37 articles.

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2. Brandel JF, Delasnerie-Laupretre N (1997) Creutzfeldt–Jakob disease and stress. J Neurol 62:541

3. Brown P, Cathala F, Sadowsky D, Gajdusek DC (1979) Creutzfeldt–Jakob disease in France: III. Epidemiological study of 170 patients dying during the decade 1968–1977. Ann Neurol 6:438–446

4. Budka H, Aguzzi A, Brown P, Brucher JM, Bugiani O, Gullotta F, Haltia M, Hauw JJ, Ironside JW, Jellinger K et al (1995) Neuropathological diagnostic criteria for Creutzfeldt–Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases). Brain Pathol 5:459–466

5. Chapman J, Ben-Israel J, Goldhammer Y, Korczyn AD (1994) The risk of developing Creutzfeldt–Jakob disease in subjects with the PRNP gene codon 200 point mutation. Neurology 44:1683–1686

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