The DYT1 carrier state increases energy demand in the olivocerebellar network.
(41/87)
(+info)
Neuronal degeneration in autonomic nervous system of Dystonia musculorum mice.
(42/87)
(+info)
Motor unit abnormalities in Dystonia musculorum mice.
(43/87)
(+info)
TorsinA participates in endoplasmic reticulum-associated degradation.
(44/87)
(+info)
Dimerization of the DYT6 dystonia protein, THAP1, requires residues within the coiled-coil domain.
(45/87)
(+info)
Sporadic adult onset primary torsion dystonia is a genetic disorder by the temporal discrimination test.
(46/87)
(+info)
An anticholinergic reverses motor control and corticostriatal LTD deficits in Dyt1 DeltaGAG knock-in mice.
(47/87)
(+info)
Abnormal nuclear envelope in the cerebellar Purkinje cells and impaired motor learning in DYT11 myoclonus-dystonia mouse models.
(48/87)
(+info)