Literature DB >> 16364674

Movement disorders and Creutzfeldt-Jakob disease: a review.

David Maltête1, Lucie Guyant-Maréchal, Bruno Mihout, Didier Hannequin.   

Abstract

Movement disorders are reported in a significant number of patients within the course of Creutzfeldt-Jakob disease (CJD). Although myoclonus is more frequent, dystonia, choreoathetosis, tremor, hemiballismus, and atypical parkinsonian syndromes have also been reported. In this review, we report the principal movement disorders associated with CJD and evaluate their correlations with neuroradiological and neuropathological findings that could in fact suggest a basal ganglia dysfunction. Further studies are warranted in order to clarify these correlations.

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Year:  2005        PMID: 16364674     DOI: 10.1016/j.parkreldis.2005.10.004

Source DB:  PubMed          Journal:  Parkinsonism Relat Disord        ISSN: 1353-8020            Impact factor:   4.891


  19 in total

1.  Striatal volume differences between non-human and human primates.

Authors:  Dali Yin; Francisco E Valles; Massimo S Fiandaca; John Forsayeth; Paul Larson; Phillip Starr; Krystof S Bankiewicz
Journal:  J Neurosci Methods       Date:  2008-09-02       Impact factor: 2.390

2.  Isolated spasticity in sporadic Creutzfeldt-Jakob disease.

Authors:  Milena Marek; Thomas Klockgether; Horst Urbach; Inga Zerr; Hans Kretzschmar; Sebastian Paus
Journal:  J Neurol       Date:  2012-11-16       Impact factor: 4.849

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.  A Corticobasal Syndrome Variant of Familial Creutzfeldt-Jakob Disease with Stroke-Like Onset.

Authors:  Ján Necpál; Martin Stelzer; Silvia Koščová; Michal Patarák
Journal:  Case Rep Neurol Med       Date:  2016-10-10

5.  A Case of Sporadic Creutzfeldt-Jakob Disease Presenting as Conversion Disorder.

Authors:  Nikhil Yegya-Raman; Rehan Aziz; Daniel Schneider; Anthony Tobia; Megan Leitch; Onyi Nwobi
Journal:  Case Rep Psychiatry       Date:  2017-05-03

6.  Codon 141 polymorphisms of the ovine prion protein gene affect the phenotype of classical scrapie transmitted from goats to sheep.

Authors:  Timm Konold; Laura J Phelan; Ben R Donnachie; Melanie J Chaplin; Saira Cawthraw; Lorenzo González
Journal:  BMC Vet Res       Date:  2017-05-04       Impact factor: 2.741

7.  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

8.  Creutzfeldt-Jakob Disease in a Tertiary Care Hospital in Thailand: A Case Series and Review of the Literature.

Authors:  Praween Lolekha; Ahmed Rasheed; Chutanat Yotsarawat
Journal:  J Mov Disord       Date:  2015-09-10

9.  Brain dopamine transporter binding and glucose metabolism in progressive supranuclear palsy-like creutzfeldt-jakob disease.

Authors:  Eero Rissanen; Valtteri Kaasinen; Pirkko Sonninen; Matias Röyttä; Markku Päivärinta
Journal:  Case Rep Neurol       Date:  2014-01-31

10.  Role of the biomarkers for the diagnosis of Creutzfeldt-Jakob disease.

Authors:  A Dulamea; E Solomon
Journal:  J Med Life       Date:  2016 Apr-Jun
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