|
Dystonia, Primary
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
Voices of 14 patients aged ≥18years (males = 7 and females = 7) with primary dystonia (DYT1 gene mutation dystonia = 4, cervical dystonia = 6, and generalized dystonia = 4) with bilateral GPi DBS were assessed.
|
30879706 |
2019 |
|
Dystonia, Primary
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
The aim of our study was to assess the association of TOR1A and THAP1 with adult-onset primary focal dystonia (AOPFD), the most common subtype of primary dystonia.
|
26803725 |
2016 |
|
Dystonia, Primary
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
The classical familial form of primary dystonia is caused by the DYT1 (ΔE) mutation in TOR1A, which encodes torsinA, AAA⁺ ATPase resident in the lumen of the endoplasmic reticular/nuclear envelope.
|
24937429 |
2014 |
|
Dystonia, Primary
|
0.400 |
Biomarker
|
disease |
BEFREE |
Genetics and pathophysiology of primary dystonia with special emphasis on DYT1 and DYT5.
|
25192508 |
2014 |
|
Dystonia, Primary
|
0.400 |
Biomarker
|
disease |
BEFREE |
This knowledge may help scientists understand the etiology of DYT1 primary dystonia, a movement disorder caused by a single glutamate deletion in TorsinA.
|
25149450 |
2014 |
|
Dystonia, Primary
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
The detailed search up to December 24, 2012, identified 24 hereditary primary dystonias (DYT1 to DYT 25) that are mostly monogenic disorders, and a larger group (>70) of genetic syndromes in which dystonia is one of the characteristic clinical features.
|
23911094 |
2014 |
|
Dystonia, Primary
|
0.400 |
Biomarker
|
disease |
CTD_human |
Mutations in GNAL cause primary torsion dystonia.
|
23222958 |
2013 |
|
Dystonia, Primary
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
The rs1801968" genes_norm="1861">D216H polymorphism (rs1801968) in TOR1A has been suggested as a risk factor for developing primary dystonia in German subjects not carrying the deletion c.904-906delGAG (∆GAG).
|
23405979 |
2013 |
|
Dystonia, Primary
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
Fifty-nine unrelated patients with cervical onset or cervical involved primary dystonia and 120 neurologically normal controls from Northeast China without mutations of TOR1A and THAP1 were all screened for mutation of GNAL gene.
|
23759320 |
2013 |
|
Dystonia, Primary
|
0.400 |
Biomarker
|
disease |
BEFREE |
Our data expand the genotypic spectrum of THAP1 and strengthen the association with upper body involvement, including the cranial and cervical regions that are usually spared in DYT1-PrD.
|
23180184 |
2013 |
|
Dystonia, Primary
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
Association of rs1182 polymorphism of the DYT1 gene with primary dystonia in Chinese population.
|
23058565 |
2012 |
|
Dystonia, Primary
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
The DYT1 904-906 del GAG mutation is responsible for some of Iranian dystonia patients, and screening for the DYT1 deletion is significant in cases with the generalized type of primary dystonia.
|
22487959 |
2012 |
|
Dystonia, Primary
|
0.400 |
Biomarker
|
disease |
BEFREE |
To date, there have been few candidate gene studies for primary dystonia and only two DYT genes, TOR1A and THAP1, have been assessed.
|
22172551 |
2012 |
|
Dystonia, Primary
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
Fourteen subjects with primary dystonia (9 carriers of the DYT1 mutation and 5 sporadic cases) were compared to 11 controls, using a simplified reference tissue model to measure binding potential.
|
21370265 |
2011 |
|
Dystonia, Primary
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
In the current study, we determined whether similar changes are also present in clinically manifesting DYT1 carriers as well as in carriers of other primary dystonia mutations such as DYT6.
|
21515903 |
2011 |
|
Dystonia, Primary
|
0.400 |
Biomarker
|
disease |
BEFREE |
TOR1A(DYT1) and the transcription factor THAP1(DYT6) are the only genes identified thus far for primary dystonia.
|
20865765 |
2010 |
|
Dystonia, Primary
|
0.400 |
Biomarker
|
disease |
BEFREE |
Clinical presentation and DYT1 status amongst Chinese patients with primary dystonia have not been well studied.
|
20113340 |
2010 |
|
Dystonia, Primary
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
Second, Exon 5 mutations in TOR1A are rarely associated with non-generalized primary dystonia.
|
19284587 |
2009 |
|
Dystonia, Primary
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
A critical question, given the 30% penetrance of clinical symptoms in DYT1 mutation carriers, is why the same genotype leads to differential clinical expression and whether non-DYT1 adult-onset primary dystonia, with and without family history share pathophysiological mechanisms with DYT1 dystonia.
|
19344776 |
2009 |
|
Dystonia, Primary
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
DYT1 dystonia is the most common form of inherited primary dystonia.
|
18224570 |
2008 |
|
Dystonia, Primary
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
To study stereotactic magnetic resonance imaging (MRI) features of the basal ganglia in DYT1 primary dystonia.
|
18477841 |
2008 |
|
Dystonia, Primary
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
We assessed the frequency of the GAG deletion in the DYT1 gene in a group of 61 Polish probands with clinical diagnosis of primary dystonia.
|
17539945 |
2007 |
|
Dystonia, Primary
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
We recruited 8 DYT1 gene carriers with dystonia, 6 DYT1 gene carriers without dystonia, 6 patients with sporadic primary dystonia (torticollis), and 10 healthy control subjects.Groups were age-matched.
|
17078060 |
2006 |
|
Dystonia, Primary
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
We screened 54 patients with primary dystonia (focal: n=41; segmental: n=11; multifocal: n=1; generalized: n=1) for the deletions in the DYT1 gene.
|
16631205 |
2006 |
|
Dystonia, Primary
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
We conclude that DYT1 mutation is a minor cause of primary dystonias in a cohort of Taiwanese population.
|
16198613 |
2006 |