Literature DB >> 9266162

Idiopathic, myoclonic and Dopa-responsive dystonia.

T Gasser1.   

Abstract

The clinical manifestations and the present status of our knowledge of the genetics of the idiopathic, myoclonic and Dopa-responsive dystonias are reviewed. The relevance of recent genetic findings to the classification of the idiopathic dystonias and to the molecular pathogenesis of Dopa-responsive dystonia are emphasized.

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Year:  1997        PMID: 9266162     DOI: 10.1097/00019052-199708000-00013

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


  2 in total

1.  Search for a founder mutation in idiopathic focal dystonia from Northern Germany.

Authors:  C Klein; L J Ozelius; J Hagenah; X O Breakefield; N J Risch; P Vieregge
Journal:  Am J Hum Genet       Date:  1998-12       Impact factor: 11.025

2.  Managing antipsychotic-induced acute and tardive dystonia.

Authors:  M Raja
Journal:  Drug Saf       Date:  1998-07       Impact factor: 5.606

  2 in total

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