Striatal neuronal loss correlates with clinical motor impairment in Huntington's disease. - Wikidata - wikimedia - TriplyDB

Striatal neuronal loss correlates with clinical motor impairment in Huntington's disease.

Striatal neuronal loss correlates with clinical motor impairment in Huntington's disease.

http://www.wikidata.org/entity/Q36269123

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Determinants of functional disability in Huntington's disease: role of cognitive and motor dysfunction Magnetic resonance imaging striatal volumes: a biomarker for clinical trials in Huntington's disease SorCS2-mediated NR2A trafficking regulates motor deficits in Huntington's disease Young-onset dementia Gait in Huntington's disease and the stride length-cadence relationship Phosphorylation of mutant huntingtin at serine 116 modulates neuronal toxicity.The HTT CAG-Expansion Mutation Determines Age at Death but Not Disease Duration in Huntington Disease nNOS(+) striatal neurons, a subpopulation spared in Huntington's Disease, possess functional NMDA receptors but fail to generate mitochondrial ROS in response to an excitotoxic challenge Complex motor task associated with non-linear BOLD responses in cerebro-cortical areas and cerebellum.Striatal parvalbuminergic neurons are lost in Huntington's disease: implications for dystonia Foxa1 is essential for development and functional integrity of the subthalamic nucleus.Early dysfunction and progressive degeneration of the subthalamic nucleus in mouse models of Huntington's disease Mapping the order and pattern of brain structural MRI changes using change-point analysis in premanifest Huntington's disease.Astrocytes are key but indirect contributors to the development of the symptomatology and pathophysiology of Huntington's disease.MicroRNAs in Neurocognitive Dysfunctions: New Molecular Targets for Pharmacological Treatments?Transcriptome sequencing reveals aberrant alternative splicing in Huntington's disease.Microtransplantation of whole ganglionic eminence cells ameliorates motor deficit, enlarges the volume of grafts, and prolongs survival in a rat model of Huntington's disease.Globus pallidus degeneration and clinicopathological features of Huntington disease.Involvement of mGlu5 receptor in 3-nitropropionic acid-induced oxidative stress in rat striatum.Reduced striato-cortical and inhibitory transcallosal connectivity in the motor circuit of Huntington's disease patients.Brain MRI Pattern Recognition Translated to Clinical Scenarios.Age-related decrease of functional connectivity additional to gray matter atrophy in a network for movement initiation

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Striatal neuronal loss correlates with clinical motor impairment in Huntington's disease.

http://www.wikidata.org/entity/Q36269123

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2012 nî lūn-bûn

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2012年の論文

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年學術文章

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2012年學術文章

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2012年學術文章

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name

Striatal neuronal loss correlates with clinical motor impairment in Huntington's disease.

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Striatal neuronal loss correlates with clinical motor impairment in Huntington's disease.

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type

label

Striatal neuronal loss correlates with clinical motor impairment in Huntington's disease.

@ast

Striatal neuronal loss correlates with clinical motor impairment in Huntington's disease.

@en

prefLabel

Striatal neuronal loss correlates with clinical motor impairment in Huntington's disease.

@ast

Striatal neuronal loss correlates with clinical motor impairment in Huntington's disease.

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Movement Disorders

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Striatal neuronal loss correlates with clinical motor impairment in Huntington's disease.

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Adam Rosenblatt

http://www.w3.org/2001/XMLSchema#string

Barbara J Crain

http://www.w3.org/2001/XMLSchema#string

Brent A Orr

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Gay Rudow

http://www.w3.org/2001/XMLSchema#string

Juan C Troncoso

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Kari-Elise Codispoti

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Olga Pletnikova

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Russell L Margolis

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Wenzhen Duan

http://www.w3.org/2001/XMLSchema#string

Zhihong Guo

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P2860

“Mini-mental state”

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

Early changes in Huntington's disease patient brains involve alterations in cytoskeletal and synaptic elements

Huntington's disease

Primate models of movement disorders of basal ganglia origin

Longitudinal change in regional brain volumes in prodromal Huntington disease

The subthalamic nucleus, hemiballismus and Parkinson's disease: reappraisal of a neurosurgical dogma.

Differential loss of striatal projection neurons in Huntington disease.

Hemiballism: report of 25 cases.

Huntington's disease: from molecular pathogenesis to clinical treatment.

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1379-1386

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scholarly article

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10.1002/MDS.25159

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11

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27

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Christopher A Ross

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2012-09-13T00:00:00Z

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22975850

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corpus striatum

Huntington disease

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3455126

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