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Related Experiment Video

Updated: Jan 30, 2026

Eye-Tracking Control to Assess Cognitive Functions in Patients with Amyotrophic Lateral Sclerosis
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Functional Biomarkers for Amyotrophic Lateral Sclerosis.

William Huynh1,2, Thanuja Dharmadasa1, Steve Vucic3

  • 1Brain and Mind Centre, University of Sydney, Sydney, NSW, Australia.

Frontiers in Neurology
|January 22, 2019
PubMed
Summary

Diagnosing amyotrophic lateral sclerosis (ALS) is challenging due to mixed motor neuron signs. This review explores novel, non-invasive electrophysiological techniques as potential biomarkers for assessing upper motor neuron (UMN) and lower motor neuron (LMN) dysfunction in ALS patients.

Keywords:
amyotrophic lateral sclerosiscortical excitabilitymotor neuron diseaseneurophysiological biomarkerstranscranial magnetic stimulation

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Area of Science:

  • Neuroscience
  • Neurology
  • Biomarkers

Background:

  • Clinical diagnosis of amyotrophic lateral sclerosis (ALS) depends on identifying progressive dysfunction in cortical, spinal, and bulbar motor neurons.
  • Clinical heterogeneity in ALS, stemming from variable upper motor neuron (UMN) and lower motor neuron (LMN) signs, often leads to diagnostic delays and challenges in monitoring disease progression and treatment efficacy, especially in clinical trials.

Purpose of the Study:

  • To provide an overview of novel, non-invasive electrophysiological techniques for assessing UMN and LMN dysfunction in ALS.
  • To highlight the potential of these techniques as biomarkers for improved diagnosis and monitoring of ALS.

Main Methods:

  • Review of recently developed non-invasive electrophysiological techniques.
  • Focus on techniques applicable to assessing both UMN and LMN function.

Main Results:

  • Emerging non-invasive electrophysiological methods show promise as biomarkers.
  • These techniques offer potential for objective assessment of motor neuron integrity in ALS.

Conclusions:

  • Novel non-invasive electrophysiological techniques represent a significant advancement in ALS research.
  • These methods may overcome current diagnostic and monitoring limitations, facilitating better patient management and clinical trial design for amyotrophic lateral sclerosis.