Literature DB >> 8858188

Chorea.

K M Shannon1.   

Abstract

The Huntington's disease mutation and its protein product are widely expressed in the brain, although the link to presumed excitotoxic damage is unknown. The availability of the genetic test increased the study of preclinical changes in the disease and the identification of more rare choreic illnesses. Other types of transient or permanent basal ganglia dysfunction might cause chorea.

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Year:  1996        PMID: 8858188     DOI: 10.1097/00019052-199608000-00010

Source DB:  PubMed          Journal:  Curr Opin Neurol        ISSN: 1350-7540            Impact factor:   5.710


  1 in total

1.  Combining Literature Review With a Ground Truth Approach for Diagnosing Huntington's Disease Phenocopy.

Authors:  Quang Tuan Rémy Nguyen; Juan Dario Ortigoza Escobar; Jean-Marc Burgunder; Caterina Mariotti; Carsten Saft; Lena Elisabeth Hjermind; Katia Youssov; G Bernhard Landwehrmeyer; Anne-Catherine Bachoud-Lévi
Journal:  Front Neurol       Date:  2022-02-10       Impact factor: 4.086

  1 in total

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