Literature DB >> 23557959

Inherited forms of Creutzfeldt-Jakob disease.

A J Degnan1, L M Levy.   

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Year:  2013        PMID： 23557959      PMCID： PMC7965612          DOI： 10.3174/ajnr.A3580

Source DB:  PubMed          Journal:  AJNR Am J Neuroradiol        ISSN： 0195-6108            Impact factor:   3.825


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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

2.  Signal transduction through prion protein.

Authors:  S Mouillet-Richard; M Ermonval; C Chebassier; J L Laplanche; S Lehmann; J M Launay; O Kellermann
Journal:  Science       Date:  2000-09-15       Impact factor: 47.728

3.  Early cognitive decline is associated with prion protein codon 129 polymorphism.

Authors:  Esther A Croes; Bart Dermaut; Jeanine J Houwing-Duistermaat; Marleen Van den Broeck; Marc Cruts; Monique M B Breteler; Albert Hofman; Christine van Broeckhoven; Cornelia M van Duijn
Journal:  Ann Neurol       Date:  2003-08       Impact factor: 10.422

Review 4.  Review: Creutzfeldt-Jakob disease: prion protein type, disease phenotype and agent strain.

Authors:  M W Head; J W Ironside
Journal:  Neuropathol Appl Neurobiol       Date:  2012-06       Impact factor: 8.090

5.  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

6.  Polymorphism at codon 129 of the prion protein gene is not associated with sporadic AD.

Authors:  O Combarros; M Sánchez-Guerra; J Llorca; A Alvarez-Arcaya; J Berciano; N Peña; C Fernández-Viadero
Journal:  Neurology       Date:  2000-08-22       Impact factor: 9.910

Review 7.  Sporadic human prion diseases: molecular insights and diagnosis.

Authors:  Gianfranco Puoti; Alberto Bizzi; Gianluigi Forloni; Jiri G Safar; Fabrizio Tagliavini; Pierluigi Gambetti
Journal:  Lancet Neurol       Date:  2012-07       Impact factor: 44.182

8.  A novel protective prion protein variant that colocalizes with kuru exposure.

Authors:  Simon Mead; Jerome Whitfield; Mark Poulter; Paresh Shah; James Uphill; Tracy Campbell; Huda Al-Dujaily; Holger Hummerich; Jon Beck; Charles A Mein; Claudio Verzilli; John Whittaker; Michael P Alpers; John Collinge
Journal:  N Engl J Med       Date:  2009-11-19       Impact factor: 91.245

Review 9.  Biology and genetics of prion diseases.

Authors:  S B Prusiner
Journal:  Annu Rev Microbiol       Date:  1994       Impact factor: 15.500

10.  Clinical aspects of common genetic Creutzfeldt-Jakob disease.

Authors:  Gabi Schelzke; Hans A Kretzschmar; Inga Zerr
Journal:  Eur J Epidemiol       Date:  2012-03-02       Impact factor: 8.082
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