Pages that link to "Q28185777"
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The following pages link to Classification and genetics of dystonia (Q28185777):
Displaying 44 items.
- Relative tissue expression of homologous torsinB correlates with the neuronal specific importance of DYT1 dystonia-associated torsinA (Q22001542) (← links)
- Mutations in the Na /K -ATPase alpha3 gene ATP1A3 are associated with rapid-onset dystonia parkinsonism (Q24299614) (← links)
- Mutations in the THAP1 gene are responsible for DYT6 primary torsion dystonia (Q24324167) (← links)
- A mutation of beta -actin that alters depolymerization dynamics is associated with autosomal dominant developmental malformations, deafness, and dystonia (Q24546532) (← links)
- Increased sensorimotor network activity in DYT1 dystonia: a functional imaging study (Q24619218) (← links)
- Treating complex movement disorders in children with cerebral palsy (Q24644664) (← links)
- Dystonia and Tremor: The Clinical Syndromes with Isolated Tremor (Q26751639) (← links)
- Therapeutic applications of botulinum neurotoxins in head and neck disorders (Q27024303) (← links)
- Mutations in PNKD causing paroxysmal dyskinesia alters protein cleavage and stability (Q28235413) (← links)
- DYT16, a novel young-onset dystonia-parkinsonism disorder: identification of a segregating mutation in the stress-response protein PRKRA (Q28267025) (← links)
- Dystonin/Bpag1 is a necessary endoplasmic reticulum/nuclear envelope protein in sensory neurons (Q28586388) (← links)
- Differential involvement of striosome and matrix dopamine systems in a transgenic model of dopa-responsive dystonia. (Q30483340) (← links)
- An African–American family with dystonia (Q30502518) (← links)
- Severe dystonia, cerebellar atrophy, and cardiomyopathy likely caused by a missense mutation in TOR1AIP1. (Q30617405) (← links)
- The anatomical basis of dystonia: current view using neuroimaging (Q30657771) (← links)
- A systematic review on the diagnosis and treatment of primary (idiopathic) dystonia and dystonia plus syndromes: report of an EFNS/MDS-ES Task Force (Q33244571) (← links)
- Distinguishing SWEDDs patients with asymmetric resting tremor from Parkinson's disease: a clinical and electrophysiological study (Q34376763) (← links)
- Primary dystonia: conceptualizing the disorder through a structural brain imaging lens (Q34682292) (← links)
- Genetic and clinical features of primary torsion dystonia (Q34777884) (← links)
- Clinical implications of pharmacogenomics for tardive dyskinesia (Q35712215) (← links)
- Whole-genome sequencing for optimized patient management (Q35857612) (← links)
- Epidemiology of primary dystonia (Q35920100) (← links)
- Functional Connectivity Networks in Asymptomatic and Symptomatic DYT1 Carriers. (Q36084267) (← links)
- Influence of coffee drinking and cigarette smoking on the risk of primary late onset blepharospasm: evidence from a multicentre case control study (Q36227210) (← links)
- The functional neuroanatomy of dystonia (Q36340491) (← links)
- Neuropathology of cervical dystonia (Q36605114) (← links)
- Recent advances in the molecular pathogenesis of dystonia-plus syndromes and heredodegenerative dystonias. (Q36634147) (← links)
- Subtle microstructural changes of the striatum in a DYT1 knock-in mouse model of dystonia (Q36774120) (← links)
- Task-specific dystonias: a review (Q37121030) (← links)
- Rare causes of dystonia parkinsonism (Q37778764) (← links)
- Molecular pathways in dystonia (Q37816579) (← links)
- Milestones in dystonia (Q37882600) (← links)
- Animal models for drug discovery in dystonia (Q38088284) (← links)
- Advances in the genetics of primary torsion dystonia (Q42413937) (← links)
- Psychiatric disorders in primary focal dystonia and in Parkinson's disease (Q42723325) (← links)
- RNA interference-mediated inhibition of wild-type Torsin A expression increases apoptosis caused by oxidative stress in cultured cells (Q42826884) (← links)
- Deep-brain stimulation for dystonia: new twists in assessment (Q48271487) (← links)
- A rare variant in TOR1A exon 5 associated with isolated dystonia in southwestern Chinese (Q48661429) (← links)
- Exome sequencing identifies GCDH (glutaryl-CoA dehydrogenase) mutations as a cause of a progressive form of early-onset generalized dystonia (Q48903075) (← links)
- Frequency of psychiatric disorders in blepharospasm does not differ from hemifacial spasm. (Q49023226) (← links)
- Unbalanced whole arm translocation resulting in loss of 18p in dystonia. (Q53632201) (← links)
- Long-term quality of life in cervical dystonia after treatment with abobotulinum toxin A: a 2-year prospective study. (Q55100812) (← links)
- [Athetosis or dystonia?] (Q80800839) (← links)
- Neuroimaging Applications in Dystonia (Q93350457) (← links)