DYT1 dystonia, a severe form of genetically determined human dystonia, exhibits reduced penetrance among carriers and begins usually during adolescence. The reasons for such age dependence and variability remain unclear
Dystonia has been defined as a syndrome of involuntary, sustained muscle contractions affecting one ...
AbstractOur understanding of how genotype determines phenotype in primary dystonia is limited. Famil...
Dystonia has been defined as a syndrome of involuntary, sustained muscle contractions affecting one ...
DYT1 dystonia, a severe form of genetically determined human dystonia, exhibits reduced penetrance a...
DYT1 dystonia, a severe form of genetically determined human dystonia, exhibits reduced penetrance a...
DYT1 dystonia, a severe form of genetically determined human dystonia, exhibits reduced penetrance a...
Purpose To study striatal dopamine D-2 receptor availability in DYT11 mutation carriers of the autos...
Striatal cholinergic dysfunction is a common phenotype associated with various forms of dystonia in ...
Striatal cholinergic dysfunction is a common phenotype associated with various forms of dystonia in ...
Dystonia is a neurological condition characterized by abnormal involuntary movements or postures owi...
Dystonia is a movement disorder of both genetic and non-genetic causes, which typically results in t...
Our understanding of how genotype determines phenotype in primary dystonia is limited. Familial youn...
Dystonia has been defined as a syndrome of involuntary, sustained muscle contractions affecting one ...
AbstractOur understanding of how genotype determines phenotype in primary dystonia is limited. Famil...
Dystonia has been defined as a syndrome of involuntary, sustained muscle contractions affecting one ...
DYT1 dystonia, a severe form of genetically determined human dystonia, exhibits reduced penetrance a...
DYT1 dystonia, a severe form of genetically determined human dystonia, exhibits reduced penetrance a...
DYT1 dystonia, a severe form of genetically determined human dystonia, exhibits reduced penetrance a...
Purpose To study striatal dopamine D-2 receptor availability in DYT11 mutation carriers of the autos...
Striatal cholinergic dysfunction is a common phenotype associated with various forms of dystonia in ...
Striatal cholinergic dysfunction is a common phenotype associated with various forms of dystonia in ...
Dystonia is a neurological condition characterized by abnormal involuntary movements or postures owi...
Dystonia is a movement disorder of both genetic and non-genetic causes, which typically results in t...
Our understanding of how genotype determines phenotype in primary dystonia is limited. Familial youn...
Dystonia has been defined as a syndrome of involuntary, sustained muscle contractions affecting one ...
AbstractOur understanding of how genotype determines phenotype in primary dystonia is limited. Famil...
Dystonia has been defined as a syndrome of involuntary, sustained muscle contractions affecting one ...