Cortical hyperexcitability may precede the onset of familial amyotrophic lateral sclerosis.
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Stronger is not always better: could a bodybuilding dietary supplement lead to ALS?Increased functional connectivity common to symptomatic amyotrophic lateral sclerosis and those at genetic riskToward precision medicine in amyotrophic lateral sclerosisChronic Glutamate Toxicity in Neurodegenerative Diseases-What is the Evidence?New developments and future opportunities in biomarkers for amyotrophic lateral sclerosisPresymptomatic studies in ALS: rationale, challenges, and approachWhat does imaging reveal about the pathology of amyotrophic lateral sclerosis?Mutant TDP-43 and FUS cause age-dependent paralysis and neurodegeneration in C. elegansINaP selective inhibition reverts precocious inter- and motorneurons hyperexcitability in the Sod1-G93R zebrafish ALS modelModeling ALS with motor neurons derived from human induced pluripotent stem cellsMotor network degeneration in amyotrophic lateral sclerosis: a structural and functional connectivity study.Environmental insults: critical triggers for amyotrophic lateral sclerosisEffect of fluoxetine on disease progression in a mouse model of ALS.The application of biomarkers in clinical trials for motor neuron diseaseAmyotrophic lateral sclerosis: a focus on disease progressionPredicting a positive response to intravenous immunoglobulin in isolated lower motor neuron syndromes.Corticomotoneuronal function and hyperexcitability in acquired neuromyotonia.A review of the neural mechanisms of action and clinical efficiency of riluzole in treating amyotrophic lateral sclerosis: what have we learned in the last decade?Corpus callosum involvement is a consistent feature of amyotrophic lateral sclerosisPersistent inward currents in spinal motoneurons: important for normal function but potentially harmful after spinal cord injury and in amyotrophic lateral sclerosis.Motor neurons and glia exhibit specific individualized responses to TDP-43 expression in a Drosophila model of amyotrophic lateral sclerosis.Delayed disease onset and extended survival in the SOD1G93A rat model of amyotrophic lateral sclerosis after suppression of mutant SOD1 in the motor cortexQuantifying disease progression in amyotrophic lateral sclerosis.Dissecting the mechanisms underlying short-interval intracortical inhibition using exercise.The Wobbler mouse model of amyotrophic lateral sclerosis (ALS) displays hippocampal hyperexcitability, and reduced number of interneurons, but no presynaptic vesicle release impairments.Human iPSC-derived motoneurons harbouring TARDBP or C9ORF72 ALS mutations are dysfunctional despite maintaining viabilityApraxia and motor dysfunction in corticobasal syndrome.Exome sequencing of case-unaffected-parents trios reveals recessive and de novo genetic variants in sporadic ALS.Presymptomatic spinal cord neurometabolic findings in SOD1-positive people at risk for familial ALS.Neurophysiological Differences between Flail Arm Syndrome and Amyotrophic Lateral Sclerosis.Controversies and priorities in amyotrophic lateral sclerosis.Investigating Default Mode and Sensorimotor Network Connectivity in Amyotrophic Lateral Sclerosis.Perception of Emotional Facial Expressions in Amyotrophic Lateral Sclerosis (ALS) at Behavioural and Brain Metabolic Level.Cortical Function in Asymptomatic Carriers and Patients With C9orf72 Amyotrophic Lateral SclerosisF Wave Study in Amyotrophic Lateral Sclerosis: Assessment of Segmental Motoneuronal DysfunctionEarly interneuron dysfunction in ALS: insights from a mutant sod1 zebrafish modelUse of biomarkers in ALS drug development and clinical trialsHyperactive somatostatin interneurons contribute to excitotoxicity in neurodegenerative disorders.Dissociation of Structural and Functional Integrities of the Motor System in Amyotrophic Lateral Sclerosis and Behavioral-Variant Frontotemporal Dementia.A randomized trial of mexiletine in ALS: Safety and effects on muscle cramps and progression
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P2860
Cortical hyperexcitability may precede the onset of familial amyotrophic lateral sclerosis.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
@zh
2008年學術文章
@zh-hant
name
Cortical hyperexcitability may ...... amyotrophic lateral sclerosis.
@en
Cortical hyperexcitability may ...... amyotrophic lateral sclerosis.
@nl
type
label
Cortical hyperexcitability may ...... amyotrophic lateral sclerosis.
@en
Cortical hyperexcitability may ...... amyotrophic lateral sclerosis.
@nl
prefLabel
Cortical hyperexcitability may ...... amyotrophic lateral sclerosis.
@en
Cortical hyperexcitability may ...... amyotrophic lateral sclerosis.
@nl
P2860
P356
P1433
P1476
Cortical hyperexcitability may ...... amyotrophic lateral sclerosis.
@en
P2093
Garth A Nicholson
P2860
P304
P356
10.1093/BRAIN/AWN071
P407
P577
2008-05-09T00:00:00Z