Altered axonal excitability properties in amyotrophic lateral sclerosis: impaired potassium channel function related to disease stage.
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New developments and future opportunities in biomarkers for amyotrophic lateral sclerosisALS as a distal axonopathy: molecular mechanisms affecting neuromuscular junction stability in the presymptomatic stages of the diseaseAxonal Dysfunction Precedes Motor Neuronal Death in Amyotrophic Lateral SclerosisElectrodiagnosis in Persons With Amyotrophic Lateral SclerosisGenetic Correction of SOD1 Mutant iPSCs Reveals ERK and JNK Activated AP1 as a Driver of Neurodegeneration in Amyotrophic Lateral Sclerosis.Abnormal electrocardiogram in a patient with amyotrophic lateral sclerosis mimicking myocardial ischaemiaEffect of fluoxetine on disease progression in a mouse model of ALS.Corticomotoneuronal function and hyperexcitability in acquired neuromyotonia.IH activity is increased in populations of slow versus fast motor axons of the ratHuman iPSC-derived motoneurons harbouring TARDBP or C9ORF72 ALS mutations are dysfunctional despite maintaining viabilityClinical Measures of Disease Progression in Amyotrophic Lateral Sclerosis.Dysfunction of axonal membrane conductances in adolescents and young adults with spinal muscular atrophyExcitability properties of motor axons in adults with cerebral palsyFlecainide in Amyotrophic Lateral Sclerosis as a Neuroprotective Strategy (FANS): A Randomized Placebo-Controlled Trial.ALS biomarkers for therapy development: State of the field and future directions.Impaired Axonal Na(+) Current by Hindlimb Unloading: Implication for Disuse Neuromuscular Atrophy.Pattern Differences of Small Hand Muscle Atrophy in Amyotrophic Lateral Sclerosis and Mimic Disorders.Assessment of nerve excitability in toxic and metabolic neuropathies.Transcranial magnetic stimulation and amyotrophic lateral sclerosis: pathophysiological insights.Decline in daily running distance presages disease onset in a mouse model of ALS.Cortical dysfunction underlies the development of the split-hand in amyotrophic lateral sclerosis.Biomarkers in amyotrophic lateral sclerosis: opportunities and limitations.The puzzling case of hyperexcitability in amyotrophic lateral sclerosis.Motoneuron firing in amyotrophic lateral sclerosis (ALS)The interplay between metabolic homeostasis and neurodegeneration: insights into the neurometabolic nature of amyotrophic lateral sclerosis.Inhibitory dysfunction in amyotrophic lateral sclerosis: future therapeutic opportunities.Impairments in Motor Neurons, Interneurons and Astrocytes Contribute to Hyperexcitability in ALS: Underlying Mechanisms and Paths to Therapy.Novel therapies in development that inhibit motor neuron hyperexcitability in amyotrophic lateral sclerosis.Intrinsic membrane hyperexcitability of amyotrophic lateral sclerosis patient-derived motor neurons.A single blind randomized controlled clinical trial of mexiletine in amyotrophic lateral sclerosis: Efficacy and safety of sodium channel blocker phase II trial.Axonal Excitability in Amyotrophic Lateral Sclerosis : Axonal Excitability in ALS.Amyotrophic lateral sclerosis: a dying motor unit?Selective mitochondrial Ca2+ uptake deficit in disease endstage vulnerable motoneurons of the SOD1G93A mouse model of amyotrophic lateral sclerosis.4-Aminopyridine Induced Activity Rescues Hypoexcitable Motor Neurons from Amyotrophic Lateral Sclerosis Patient-Derived Induced Pluripotent Stem Cells.Modeling activity-dependent changes of axonal spike conduction in primary afferent C-nociceptors.Increased HCN channel driven inward rectification in benign cramp fasciculation syndrome.Electrically evoked multiplet discharges are associated with more marked clinical deterioration in motor neuron disease.Shortcomings in the Current Amyotrophic Lateral Sclerosis Trials and Potential Solutions for Improvement.Hereditary primary lateral sclerosis with cone dysfunction.Differential expression of voltage-gated K+ currents in medial septum/diagonal band complex neurons exhibiting distinct firing phenotypes.
P2860
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P2860
Altered axonal excitability properties in amyotrophic lateral sclerosis: impaired potassium channel function related to disease stage.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
2006年论文
@zh
2006年论文
@zh-cn
name
Altered axonal excitability pr ...... tion related to disease stage.
@en
type
label
Altered axonal excitability pr ...... tion related to disease stage.
@en
prefLabel
Altered axonal excitability pr ...... tion related to disease stage.
@en
P2093
P2860
P356
P1433
P1476
Altered axonal excitability pr ...... tion related to disease stage.
@en
P2093
Hugh Bostock
Kazuaki Kanai
Kazue Ogawara
Miho Nakata
Noriko Tamura
Setsu Sawai
Sonoko Misawa
Takamichi Hattori
P2860
P304
P356
10.1093/BRAIN/AWL024
P407
P577
2006-02-08T00:00:00Z