Predominant dystonia with marked cerebellar atrophy: A rare phenotype in familial dystonia
about
The neural substrates of rapid-onset Dystonia-Parkinsonism.The basal ganglia and cerebellum interact in the expression of dystonic movementCurrent and emerging strategies for treatment of childhood dystoniaAbnormal activation of the primary somatosensory cortex in spasmodic dysphonia: an fMRI study.Focal white matter changes in spasmodic dysphonia: a combined diffusion tensor imaging and neuropathological study.Oromandibular and lingual dystonia associated with spinocerebellar ataxia type 8Alteration in forward model prediction of sensory outcome of motor action in focal hand dystonia.Alterations in cerebellar physiology are associated with a stiff-legged gait in Atcay(ji-hes) miceSevere dystonia, cerebellar atrophy, and cardiomyopathy likely caused by a missense mutation in TOR1AIP1.Altered dendritic morphology of Purkinje cells in Dyt1 ΔGAG knock-in and purkinje cell-specific Dyt1 conditional knockout mice.Abnormal nuclear envelope in the cerebellar Purkinje cells and impaired motor learning in DYT11 myoclonus-dystonia mouse modelsDefinition and classification of hyperkinetic movements in childhood.Physiologic changes associated with cerebellar dystonia.Evidence for altered basal ganglia-brainstem connections in cervical dystoniaUntethering the nuclear envelope and cytoskeleton: biologically distinct dystonias arising from a common cellular dysfunctionAnimal models of dystonia: Lessons from a mutant rat.Dystonia and cerebellar degeneration in the leaner mouse mutant.Improved motor performance in Dyt1 ΔGAG heterozygous knock-in mice by cerebellar Purkinje-cell specific Dyt1 conditional knocking-outThe functional neuroanatomy of dystonia.The genetics of dystonias.Dystonia as a network disorder: what is the role of the cerebellum?Update on the pathology of dystonia.Cerebellum: An explanation for dystonia?Current Opinions and Areas of Consensus on the Role of the Cerebellum in Dystonia.Recessive dystonia-ataxia syndrome in a Turkish family caused by a COX20 (FAM36A) mutation.Pathogenesis of dystonia: is it of cerebellar or basal ganglia origin?It's not just the basal ganglia: Cerebellum as a target for dystonia therapeutics.
P2860
Q24609728-FB7CB621-2C46-4819-AA96-256D419A8321Q24653882-8B487380-F12B-41D2-92D0-9D547DCBEC19Q27011677-699A3D91-E615-4795-AE3F-918C6CAF6058Q30473242-F6DE1471-D808-4680-9A03-906E311DF1E1Q30491506-BF1BBB08-C1E7-497E-A5AE-002D2405DB42Q30531728-2E9E2588-0F5C-44AA-9A27-7014CCD6D1CCQ30559404-2E33B9AA-F19E-4218-846B-29A122C781E7Q30580787-5AF6270C-920E-4F46-8612-62D94CD80386Q30617405-B7895B9F-0CF4-498C-BCB2-F68E61CFA3C8Q33867544-4927A9B4-C192-4D66-8F4F-21E6B33BD934Q34063055-B1B6FA00-BC9E-4476-BBA2-89F51E647C4BQ34088846-3E327B70-E4B0-4517-B2CA-E919EC296CCBQ34145378-F521AF4F-A8E3-45D1-9457-F2BEFFA5D43BQ34181828-DC23022F-B884-4BC4-8A35-E9C241650E53Q34638417-AC5353FD-B866-4AD8-8D21-E2651E353608Q35210338-A24B736A-CC0E-436F-BE1E-4166A98BC5D8Q35639062-7F76C6C2-4D9E-4741-AD04-1153C9BFDFB1Q35878028-877EBEB3-41FD-4C78-93CE-01FB2FA303A2Q36340491-76E1860D-0FDF-40BA-A4DD-C75707E46D41Q36934972-40522B8E-3728-479F-992C-26141A7C64BAQ37592345-3CD36F02-0610-47D4-BE54-557A7A9FA564Q37827217-A636247A-A338-477E-8971-189CE3145F94Q38682605-63E049F4-4992-4DA8-A689-D5D3049B865CQ38979271-86CBDF4D-772D-4D48-B2D7-0EA2DFB60C16Q44108174-E31AFB42-64FE-43E9-8245-520033AB3DE4Q47992772-FAF2F0D8-2D2B-4701-87F7-4BB21C5F1946Q48139176-CF1B97C4-A929-457A-8237-62B3F0C29605
P2860
Predominant dystonia with marked cerebellar atrophy: A rare phenotype in familial dystonia
description
im November 2006 veröffentlichter wissenschaftlicher Artikel
@de
wetenschappelijk artikel
@nl
наукова стаття, опублікована в листопаді 2006
@uk
name
Predominant dystonia with mark ...... phenotype in familial dystonia
@en
Predominant dystonia with mark ...... phenotype in familial dystonia
@nl
type
label
Predominant dystonia with mark ...... phenotype in familial dystonia
@en
Predominant dystonia with mark ...... phenotype in familial dystonia
@nl
prefLabel
Predominant dystonia with mark ...... phenotype in familial dystonia
@en
Predominant dystonia with mark ...... phenotype in familial dystonia
@nl
P2093
P1433
P1476
Predominant dystonia with mark ...... phenotype in familial dystonia
@en
P2093
A. Camuzat
A. M. Ouvrard-Hernandez
M. Viemont
N. Benamar
P. De Liege
P304
P356
10.1212/01.WNL.0000244484.60489.50
P407
P577
2006-11-27T00:00:00Z