Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6. - Wikidata - wikimedia - TriplyDB

Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6.

Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6.

http://www.wikidata.org/entity/Q45294691

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Neuroimaging of the periaqueductal gray: state of the field Motor training in degenerative spinocerebellar disease: ataxia-specific improvements by intensive physiotherapy and exergames Structural and Functional Magnetic Resonance Imaging of the Cerebellum: Considerations for Assessing Cerebellar Ataxias.In vivo structural imaging of the cerebellum, the contribution of ultra-high fields.Distinct critical cerebellar subregions for components of verbal working memory.Neural correlates of ataxia severity in spinocerebellar ataxia type 3/Machado-Joseph disease.Size of error affects cerebellar contributions to motor learning.CAG repeats determine brain atrophy in spinocerebellar ataxia 17: a VBM study.Diffusion tensor imaging reveals disease-specific deep cerebellar nuclear changes in cerebellar degeneration.Association between proton magnetic resonance spectroscopy measurements and CAG repeat number in patients with spinocerebellar ataxias 2, 3, or 6 Distinct neurochemical profiles of spinocerebellar ataxias 1, 2, 6, and cerebellar multiple system atrophy.Survival and severity in dominant cerebellar ataxias.Change in the cortical complexity of spinocerebellar ataxia type 3 appears earlier than clinical symptoms Macro- and microstructural changes in patients with spinocerebellar ataxia type 6: assessment of phylogenetic subdivisions of the cerebellum and the brain stem.Disruption of Purkinje cell function prior to huntingtin accumulation and cell loss in an animal model of Huntington disease.A longitudinal investigation into cognition and disease progression in spinocerebellar ataxia types 1, 2, 3, 6, and 7 Consensus paper: radiological biomarkers of cerebellar diseases MRI-based cerebellar volume measurements correlate with the International Cooperative Ataxia Rating Scale score in patients with spinocerebellar degeneration or multiple system atrophy.MRI shows a region-specific pattern of atrophy in spinocerebellar ataxia type 2.CAG repeat length does not associate with the rate of cerebellar degeneration in spinocerebellar ataxia type 3.Degenerative Ataxias: challenges in clinical research.Impact of cerebellar atrophy on cortical gray matter and cerebellar peduncles as assessed by voxel-based morphometry and high angular resolution diffusion imaging.Principal component analysis of cerebellar shape on MRI separates SCA types 2 and 6 into two archetypal modes of degeneration.Consensus paper: pathological mechanisms underlying neurodegeneration in spinocerebellar ataxias.Movement disorders in spinocerebellar ataxias.Polyglutamine (PolyQ) diseases: genetics to treatments.Oculomotor deficits in spinocerebellar ataxia type 3: Potential biomarkers of preclinical detection and disease progression.MR Imaging in Spinocerebellar Ataxias: A Systematic Review.Structural and functional MRI abnormalities of cerebellar cortex and nuclei in SCA3, SCA6 and Friedreich's ataxia.Cerebellum and neurodegenerative diseases: Beyond conventional magnetic resonance imaging.Cerebral cortex involvement in Machado-Joseph disease.Treatment of Spinocerebellar Ataxia With Mesenchymal Stem Cells: A Phase I/IIa Clinical Study.A multimodal evaluation of microstructural white matter damage in spinocerebellar ataxia type 3.Genetics of ataxias: hereditary forms.Selective Patterns of Cognitive Impairment in Spinocerebellar Ataxia Type 6 and Idiopathic Late-Onset Cerebellar Ataxia.Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6.Polyglutamine spinocerebellar ataxias - from genes to potential treatments.Cerebellar Involvement in Patients with Mild to Moderate Myoclonus Due to EPM1: Structural and Functional MRI Findings in Comparison with Healthy Controls and Ataxic Patients.Progressive cognitive dysfunction in spinocerebellar ataxia type 3.Flattened facial colliculus on magnetic resonance imaging in Machado-Joseph disease.

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Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6.

http://www.wikidata.org/entity/Q45294691

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2009 nî lūn-bûn

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Visualization, quantification ...... ellar ataxia types 1, 3 and 6.

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Visualization, quantification ...... ellar ataxia types 1, 3 and 6.

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Visualization, quantification ...... ellar ataxia types 1, 3 and 6.

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Visualization, quantification ...... ellar ataxia types 1, 3 and 6.

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Visualization, quantification ...... ellar ataxia types 1, 3 and 6.

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Visualization, quantification ...... ellar ataxia types 1, 3 and 6.

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Visualization, quantification ...... ellar ataxia types 1, 3 and 6.

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Alexandra Dürr

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Andrés González Mandly

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