Amyotrophic lateral sclerosis (ALS): a phylogenetic disease of the corticomotoneuron?
about
Presymptomatic studies in ALS: rationale, challenges, and approachWidespread grey matter pathology dominates the longitudinal cerebral MRI and clinical landscape of amyotrophic lateral sclerosis.Corpus callosum involvement is a consistent feature of amyotrophic lateral sclerosisThe epidemiology of ALS: a conspiracy of genes, environment and time.Delayed disease onset and extended survival in the SOD1G93A rat model of amyotrophic lateral sclerosis after suppression of mutant SOD1 in the motor cortexLockhart Clarke's contribution to the description of amyotrophic lateral sclerosis.Controversies and priorities in amyotrophic lateral sclerosis.Double cortical stimulation in amyotrophic lateral sclerosis.High signal intensity on T1 weighted MRI of the anterolateral column of the spinal cord in amyotrophic lateral sclerosis.Transcranial magnetic stimulation and amyotrophic lateral sclerosis: pathophysiological insights.Cortical dysfunction underlies the development of the split-hand in amyotrophic lateral sclerosis.ALS motor phenotype heterogeneity, focality, and spread: deconstructing motor neuron degeneration.Calretinin and Neuropeptide Y interneurons are differentially altered in the motor cortex of the SOD1G93A mouse model of ALS.Advances in the application of MRI to amyotrophic lateral sclerosis.Exercise and amyotrophic lateral sclerosis.Regional spread pattern predicts survival in patients with sporadic amyotrophic lateral sclerosis.Cortical excitability and neurology: insights into the pathophysiologyThe puzzling case of hyperexcitability in amyotrophic lateral sclerosis.Tools and talk: an evolutionary perspective on the functional deficits associated with amyotrophic lateral sclerosis.Motoneuron firing in amyotrophic lateral sclerosis (ALS)Motor neuron dysfunction in frontotemporal dementia.Inhibitory dysfunction in amyotrophic lateral sclerosis: future therapeutic opportunities.Transcranial Magnetic Stimulation for the Assessment of Neurodegenerative Disease.Novel therapies in development that inhibit motor neuron hyperexcitability in amyotrophic lateral sclerosis.Cell Death-Autophagy Loop and Glutamate-Glutamine Cycle in Amyotrophic Lateral Sclerosis.Apical dendrite degeneration, a novel cellular pathology for Betz cells in ALSUpper and extra-motoneuron involvement in early motoneuron disease: a diffusion tensor imaging study.Involvement of spinal sensory pathway in ALS and specificity of cord atrophy to lower motor neuron degeneration.Changes in the Excitability of Neocortical Neurons in a Mouse Model of Amyotrophic Lateral Sclerosis Are Not Specific to Corticospinal Neurons and Are Modulated by Advancing Disease.Cortical excitability changes distinguish the motor neuron disease phenotypes from hereditary spastic paraplegia.Cortical hyperexcitability and the split-hand plus phenomenon: pathophysiological insights in ALS.Riluzole exerts transient modulating effects on cortical and axonal hyperexcitability in ALS.Navigated transcranial magnetic stimulation in amyotrophic lateral sclerosis.Potential structural and functional biomarkers of upper motor neuron dysfunction in ALS.Cortical excitability differences in hand muscles follow a split-hand pattern in healthy controls.Riluzole exerts central and peripheral modulating effects in amyotrophic lateral sclerosis.Incorporating upper motor neuron health in ALS drug discovery.Neurotoxicity of the Cyanotoxin BMAA Through Axonal Degeneration and Intercellular Spreading.Analysis of motor unit firing characteristics in patients with motor neuron diseases.Dissociated lower limb muscle involvement in amyotrophic lateral sclerosis.
P2860
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P2860
Amyotrophic lateral sclerosis (ALS): a phylogenetic disease of the corticomotoneuron?
description
1992 nî lūn-bûn
@nan
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
1992年论文
@zh
1992年论文
@zh-cn
name
Amyotrophic lateral sclerosis (ALS): a phylogenetic disease of the corticomotoneuron?
@ast
Amyotrophic lateral sclerosis (ALS): a phylogenetic disease of the corticomotoneuron?
@en
type
label
Amyotrophic lateral sclerosis (ALS): a phylogenetic disease of the corticomotoneuron?
@ast
Amyotrophic lateral sclerosis (ALS): a phylogenetic disease of the corticomotoneuron?
@en
prefLabel
Amyotrophic lateral sclerosis (ALS): a phylogenetic disease of the corticomotoneuron?
@ast
Amyotrophic lateral sclerosis (ALS): a phylogenetic disease of the corticomotoneuron?
@en
P2093
P2860
P356
P1433
P1476
Amyotrophic lateral sclerosis (ALS): a phylogenetic disease of the corticomotoneuron?
@en
P2093
P2860
P304
P356
10.1002/MUS.880150215
P577
1992-02-01T00:00:00Z