Penetrating observations of dystonia
- 1 September 1998
- journal article
- editorial
- Published by Wiley in Annals of Neurology
- Vol. 44 (3) , 299-300
- https://doi.org/10.1002/ana.410440302
Abstract
No abstract availableThis publication has 12 references indexed in Scilit:
- Functional brain networks in DYT1 dystoniaAnnals of Neurology, 1998
- Idiopathic torsion dystonia linked to chromosome 8 in two mennonite familiesAnnals of Neurology, 1997
- The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding proteinNature Genetics, 1997
- Mutation in the α-Synuclein Gene Identified in Families with Parkinson's DiseaseScience, 1997
- Idiopathic torsion dystonia: assignment of a gene to chromosome 18p in a German family with adult onset, autosomal dominant inheritance and purely focal distributionHuman Molecular Genetics, 1996
- The metabolic topography of idiopathic torsion dystoniaBrain, 1995
- Recessively inherited L-DOPA-responsive dystonia caused by a point mutation (Q381K) in the tyrosine hydroxylase geneHuman Molecular Genetics, 1995
- Hereditary progressive dystonia with marked diurnal fluctuation caused by mutations in the GTP cyclohydrolase I geneNature Genetics, 1994
- Complex segregation analysis of dystonia pedigrees suggests autosomal dominant inheritanceNeurology, 1990
- Idiopathic dystonia among ashkenazi jews: Evidence for autosomal dominant inheritanceAnnals of Neurology, 1989