Literature DB >> 12360570

Focal dystonia as the presenting sign in Creutzfeldt-Jakob disease.

Mark A Hellmann1, Eldad Melamed.   

Abstract

A variety of movement disorders may occur during the course of prion disease. We describe a unique patient who had focal upper limb dystonia as the presenting symptom of familial codon 200 mutation-positive Creutzfeldt-Jakob disease. Copyright 2002 Movement Disorder Society

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Year:  2002        PMID: 12360570     DOI: 10.1002/mds.10232

Source DB:  PubMed          Journal:  Mov Disord        ISSN: 0885-3185            Impact factor:   10.338


  5 in total

1.  Codon 200 mutation of the prion gene: genotype-phenotype correlations.

Authors:  Peter K Panegyres; Judy G S Goh; Jack Goldblatt
Journal:  J Neurol       Date:  2012-05-15       Impact factor: 4.849

2.  Creutzfeldt-Jakob disease with E200K PRNP mutation: a case report and revision of the literature.

Authors:  Michelangelo Mancuso; Gabriele Siciliano; Sabina Capellari; Daniele Orsucci; Policarpo Moretti; Giuseppe Di Fede; Silvia Suardi; Rosaria Strammiello; Piero Parchi; Fabrizio Tagliavini; Luigi Murri
Journal:  Neurol Sci       Date:  2009-07-14       Impact factor: 3.307

Review 3.  Secondary dystonia-clinical clues and syndromic associations.

Authors:  Susanne A Schneider; Kailash P Bhatia
Journal:  J Mov Disord       Date:  2009-10-30

4.  Prevalence and Treatments of Movement Disorders in Prion Diseases: A Longitudinal Cohort Study.

Authors:  Danielle Sequeira; Akin Nihat; Tzehow Mok; Thomas Coysh; Peter Rudge; John Collinge; Simon Mead
Journal:  Mov Disord       Date:  2022-07-16       Impact factor: 9.698

5.  Sporadic Creutzfeldt-Jakob disease with focal findings: caveats to current diagnostic criteria.

Authors:  Edward C Mader; Rima El-Abassi; Nicole R Villemarette-Pittman; Lenay Santana-Gould; Piotr W Olejniczak; John D England
Journal:  Neurol Int       Date:  2013-02-15
  5 in total

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