Axonal Dysfunction Precedes Motor Neuronal Death in Amyotrophic Lateral Sclerosis

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Risk factors in Swedish young men for amyotrophic lateral sclerosis in adulthood.Synaptic dysfunction and altered excitability in C9ORF72 ALS/FTD.

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Axonal Dysfunction Precedes Motor Neuronal Death in Amyotrophic Lateral Sclerosis

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Axonal Dysfunction Precedes Motor Neuronal Death in Amyotrophic Lateral Sclerosis

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Axonal Dysfunction Precedes Motor Neuronal Death in Amyotrophic Lateral Sclerosis

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Axonal Dysfunction Precedes Motor Neuronal Death in Amyotrophic Lateral Sclerosis

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Axonal Dysfunction Precedes Motor Neuronal Death in Amyotrophic Lateral Sclerosis

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Axonal Dysfunction Precedes Motor Neuronal Death in Amyotrophic Lateral Sclerosis

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Axonal Dysfunction Precedes Motor Neuronal Death in Amyotrophic Lateral Sclerosis

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Axonal Dysfunction Precedes Motor Neuronal Death in Amyotrophic Lateral Sclerosis

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Axonal Dysfunction Precedes Motor Neuronal Death in Amyotrophic Lateral Sclerosis

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Axonal Dysfunction Precedes Motor Neuronal Death in Amyotrophic Lateral Sclerosis

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Axonal Dysfunction Precedes Motor Neuronal Death in Amyotrophic Lateral Sclerosis

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P2093

Hiroshi Amino

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

Kazumoto Shibuya

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

Keisuke Watanabe

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Satoshi Kuwabara

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

Sonoko Misawa

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Yukari Sekiguchi

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Yuta Iwai

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P2860

El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis

Excitability of human axons.

Nerve excitability studies characterize Kv1.1 fast potassium channel dysfunction in patients with episodic ataxia type 1.

Human iPSC-derived motoneurons harbouring TARDBP or C9ORF72 ALS mutations are dysfunctional despite maintaining viability

Axonal ion channels from bench to bedside: a translational neuroscience perspective.

Riluzole, neuroprotection and amyotrophic lateral sclerosis.

Excitatory amino acid neurotoxicity and neurodegenerative disease.

Can regional spreading of amyotrophic lateral sclerosis motor symptoms be explained by prion-like propagation?

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.

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e0158596

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scholarly article

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239525

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10.1371/JOURNAL.PONE.0158596

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English

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2016-01-01T00:00:00Z

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27383069

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amyotrophic lateral sclerosis

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4934877

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Axonal Dysfunction Precedes Motor Neuronal Death in Amyotrophic Lateral Sclerosis

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P2860

P2860

Axonal Dysfunction Precedes Motor Neuronal Death in Amyotrophic Lateral Sclerosis

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P1433

P1476

P2093

P2860

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P3181

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P698

P921

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P1476

P2093

P2860

P304

P31

P3181

P356

P407

P433

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