Does interneuronal dysfunction contribute to neurodegeneration in amyotrophic lateral sclerosis?

Does interneuronal dysfunction contribute to neurodegeneration in amyotrophic lateral sclerosis?

Amyotrophic lateral sclerosis (ALS) is typically regarded as a sporadic neurodegenerative disorder that results in a catastrophic failure of the motor system, with characteristically variable involvement of upper and lower motor neuronal populations. A wide range of evidence from clinical, histologi...

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Bibliografiske detaljer
Main Authors:	Turner, M, Kiernan, M
Format:	Journal article
Sprog:	English
Udgivet:	2012

Lignende værker

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Biomarkers in amyotrophic lateral sclerosis.
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Amyotrophic lateral sclerosis.
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Lockhart Clarke's contribution to the description of amyotrophic lateral sclerosis.
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Concurrent multiple sclerosis and amyotrophic lateral sclerosis: where inflammation and neurodegeneration meet?
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Concurrent multiple sclerosis and amyotrophic lateral sclerosis: where inflammation and neurodegeneration meet?
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Kinnier Wilson's puzzling features of amyotrophic lateral sclerosis
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Assessment of the upper motor neuron in amyotrophic lateral sclerosis
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Human cerebral evolution and the clinical syndrome of amyotrophic lateral sclerosis
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Controversies and priorities in amyotrophic lateral sclerosis.
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Regional callosal integrity and bilaterality of limb weakness in amyotrophic lateral sclerosis
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Neuroimaging in amyotrophic lateral sclerosis.
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Neuroimaging endpoints in amyotrophic lateral sclerosis
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Advances in the application of MRI to amyotrophic lateral sclerosis.
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Untangling neuroinflammation in amyotrophic lateral sclerosis
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Sweet food preference in amyotrophic lateral sclerosis
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The tough body at the epicentre of amyotrophic lateral sclerosis
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