Purpose To study striatal dopamine D-2 receptor availability in DYT11 mutation carriers of the autosomal dominantly inherited disorder myoclonus-dystonia (M-D). Methods Fifteen DYT11 mutation carriers ( 11 clinically affected) and 15 age- and sex-matched controls were studied using I-123-IBZM SPECT. Specific striatal binding ratios were calculated using standard templates for striatum and occipital areas. Results Multivariate analysis with corrections for ageing and smoking showed significantly lower specific striatal to occipital IBZM uptake ratios (SORs) both in the left and right striatum in clinically affected patients and also in all DYT11 mutation carriers compared to control subjects. Conclusions Our findings are consistent with the ...
DYT1 dystonia, a severe form of genetically determined human dystonia, exhibits reduced penetrance a...
Striatal dysfunction is implicated in many movement disorders. However, the precise nature of defect...
Cervical dystonia (CD) is a movement disorder accompanied by non-motor symptoms like depressive symp...
Purpose To study striatal dopamine D-2 receptor availability in DYT11 mutation carriers of the autos...
KO mice. Neuroimaging studies of DYT11 M-D patients show reduced dopamine D2 receptor (D2R) availab...
Preclinical and clinical evidence suggests that impaired gamma-aminobutyric (GABA) control, leading ...
Background:Myoclonus-dystonia (M-D) is an autosomal dominantly inherited movement disorder character...
Dystonia pathophysiology has been partly linked to downregulation and dysfunction of dopamine D2 rec...
DYT1 dystonia is an inherited disease linked to mutation in the TOR1A gene encoding for the protein ...
We have studied dopamine D-2 receptor binding by [C-11]raclopride positron emission tomography in 14...
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...
Myoclonus-dystonia is an autosomal dominantly inherited movement disorder clinically characterized b...
DYT1 dystonia, a severe form of genetically determined human dystonia, exhibits reduced penetrance a...
Striatal dysfunction is implicated in many movement disorders. However, the precise nature of defect...
Cervical dystonia (CD) is a movement disorder accompanied by non-motor symptoms like depressive symp...
Purpose To study striatal dopamine D-2 receptor availability in DYT11 mutation carriers of the autos...
KO mice. Neuroimaging studies of DYT11 M-D patients show reduced dopamine D2 receptor (D2R) availab...
Preclinical and clinical evidence suggests that impaired gamma-aminobutyric (GABA) control, leading ...
Background:Myoclonus-dystonia (M-D) is an autosomal dominantly inherited movement disorder character...
Dystonia pathophysiology has been partly linked to downregulation and dysfunction of dopamine D2 rec...
DYT1 dystonia is an inherited disease linked to mutation in the TOR1A gene encoding for the protein ...
We have studied dopamine D-2 receptor binding by [C-11]raclopride positron emission tomography in 14...
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...
Myoclonus-dystonia is an autosomal dominantly inherited movement disorder clinically characterized b...
DYT1 dystonia, a severe form of genetically determined human dystonia, exhibits reduced penetrance a...
Striatal dysfunction is implicated in many movement disorders. However, the precise nature of defect...
Cervical dystonia (CD) is a movement disorder accompanied by non-motor symptoms like depressive symp...