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Seizures in E200K familial and sporadic Creutzfeldt-Jakob disease

  • Published:2014-10-16 Issue:3 Volume:131 Page:152-157
  • ISSN:0001-6314
  • Container-title:Acta Neurologica Scandinavica
  • language:en
  • Short-container-title:Acta Neurol Scand

Author:

Appel S.1,Chapman J.23,Cohen O. S.23,Rosenmann H.4,Nitsan Z.1,Blatt I.23

Affiliation:

1. Department of Neurology; Barzilai Medical Center, affiliated to Ben Gurion University; Ashkelon Israel

2. Department of Neurology; Sheba Medical Center; Ramat-Gan Israel

3. Sackler Faculty of medicine; Tel-Aviv University; Tel Aviv Israel

4. Department of Neurology; Hadassah University Hospital; Jerusalem Israel

Funder

NIH

Publisher

Wiley

Subject

Clinical Neurology,Neurology,General Medicine

Reference15 articles.

1. Prion protein genotype and pathological phenotype studies in sporadic Creutzfeldt-Jakob disease;Macdonald;Neuropathol Appl Neurobiol,1996

2. Prion diseases;Knight;J Neurol Neurosurg Psychiatry,2004

3. Mutation in codon 200 of scrapie amyloid precursor gene linked to Creutzfeldt-Jakob disease in Sephardic Jews of Libyan and non-Libyan origin;Goldfarb;Lancet,1990

4. Familial Creutzfeldt-Jakob disease presenting as epilepsia partialis continua;Lowden;Epileptic Disord,2008

5. Sporadic Creutzfeldt-Jakob disease presenting as nonconvulsive status epilepticus, case report and review of the literature;Espinosa;Clin Neurol Neurosurg,2010

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