Literature DB >> 17334659

Two Norwegian sisters with late onset Creutzfeldt-Jakob disease caused by the E200K mutation.

Elisabeth Farbu, Ole-Bjørn Tysnes, Sverre Mørk, Bård K Krossnes, Laurence A Bindoff.   

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Year:  2007        PMID： 17334659     DOI： 10.1007/s00415-006-0363-0

Source DB:  PubMed          Journal:  J Neurol        ISSN： 0340-5354            Impact factor:   4.849


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  5 in total

Review 1.  Familial Creutzfeldt-Jakob disease. Codon 200 prion disease in Libyan Jews.

Authors:  Z Meiner; R Gabizon; S B Prusiner
Journal:  Medicine (Baltimore)       Date:  1997-07       Impact factor: 1.889

2.  Mutations in familial Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker's syndrome.

Authors:  D Goldgaber; L G Goldfarb; P Brown; D M Asher; W T Brown; S Lin; J W Teener; S M Feinstone; R Rubenstein; R J Kascsak
Journal:  Exp Neurol       Date:  1989-11       Impact factor: 5.330

3.  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

4.  Mutation in codon 200 and polymorphism in codon 129 of the prion protein gene in Libyan Jews with Creutzfeldt-Jakob disease.

Authors:  R Gabizon; H Rosenman; Z Meiner; I Kahana; E Kahana; Y Shugart; J Ott; S B Prusiner
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  1994-03-29       Impact factor: 6.237

Review 5.  Sporadic and familial CJD: classification and characterisation.

Authors:  Pierluigi Gambetti; Qingzhong Kong; Wenquan Zou; Piero Parchi; Shu G Chen
Journal:  Br Med Bull       Date:  2003       Impact factor: 4.291
  5 in total

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