Literature DB >> 1761102

Creutzfeldt-Jakob disease in the last 5 years in Hungary.

K Maytenyi1.   

Abstract

Mesh：

Year:  1991        PMID： 1761102     DOI： 10.1007/bf00143121

Source DB:  PubMed          Journal:  Eur J Epidemiol        ISSN： 0393-2990            Impact factor:   8.082


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  4 in total

1.  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

2.  Creutzfeldt-Jakob disease and kuru patients lack a mutation consistently found in the Gerstmann-Sträussler-Scheinker syndrome.

Authors:  L G Goldfarb; P Brown; D Goldgaber; D M Asher; R Rubenstein; W T Brown; P Piccardo; R J Kascsak; J W Boellaard; D C Gajdusek
Journal:  Exp Neurol       Date:  1990-06       Impact factor: 5.330

3.  Creutzfeldt-Jakob disease. II. Clinical, pathologic, and genetic study of a family.

Authors:  W W May; H H Itabashi; R N De Jong
Journal:  Arch Neurol       Date:  1968-08

4.  Creutzfeldt-Jakob disease: patterns of worldwide occurrence and the significance of familial and sporadic clustering.

Authors:  C L Masters; J O Harris; D C Gajdusek; C J Gibbs; C Bernoulli; D M Asher
Journal:  Ann Neurol       Date:  1979-02       Impact factor: 10.422
  4 in total
  1 in total

1.  Human prion diseases in the United States.

Authors:  Robert C Holman; Ermias D Belay; Krista Y Christensen; Ryan A Maddox; Arialdi M Minino; Arianne M Folkema; Dana L Haberling; Teresa A Hammett; Kenneth D Kochanek; James J Sejvar; Lawrence B Schonberger
Journal:  PLoS One       Date:  2010-01-01       Impact factor: 3.240
  1 in total

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