Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Simplifying the approach: what can we do?

M J Strong1

  • 1London Health Sciences Centre, University of Western Ontario, Canada. mstrong@julian.uwo.ca

Neurology
|November 24, 1999
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Use of lumbar laminoplasty vs. laminotomy for transection of the filum terminale does not affect early complication rates or postoperative course.

Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery·2015
Same author

Expression and cellular localization of the classical progesterone receptor in healthy and amyotrophic lateral sclerosis affected spinal cord.

European journal of neurology·2014
Same author

Multiple cerebral infarcts in patient with Moyamoya disease.

The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques·2012
Same author

Regional spread pattern predicts survival in patients with sporadic amyotrophic lateral sclerosis.

European journal of neurology·2012
Same author

Practice parameter update: the care of the patient with amyotrophic lateral sclerosis: drug, nutritional, and respiratory therapies (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology.

Neurology·2009
Same author

Practice parameter update: the care of the patient with amyotrophic lateral sclerosis: multidisciplinary care, symptom management, and cognitive/behavioral impairment (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology.

Neurology·2009
Same journal

Factors Associated With Disability Improvement and Worsening Independent of Attacks in Patients With AQP4-IgG+ NMOSD and MOGAD: A Multicenter Cohort Study.

Neurology·2026
Same journal

Cost-Effectiveness of Intracranial Aneurysm Screening: A Systematic Review.

Neurology·2026
Same journal

Rare Eating Epilepsy: Co-Occurrence of Focal Cortical Dysplasia and Gray Matter Heterotopia.

Neurology·2026
Same journal

Spatiotemporal Associations Between Cortical Microinfarcts and Cortical Superficial Siderosis in Cerebral Amyloid Angiopathy.

Neurology·2026
Same journal

Blood-Brain Barrier Disruption Before Interhospital Transfer for Thrombectomy and Clinical Outcome.

Neurology·2026
Same journal

At Death's Door: Cytosolic Dopamine in Patients With Parkinson Disease.

Neurology·2026
See all related articles

Simplifying the diagnosis of amyotrophic lateral sclerosis (ALS) is challenging. Current diagnostic methods, including electrophysiology and imaging, require further validation for reliable and early ALS detection.

Area of Science:

  • Neurology
  • Diagnostic Medicine

Background:

  • Diagnosing amyotrophic lateral sclerosis (ALS) presents significant challenges.
  • Current diagnostic approaches often lack simplicity and universal applicability.

Purpose of the Study:

  • To explore potential strategies for simplifying the diagnostic process of ALS.
  • To evaluate the utility of emerging diagnostic techniques in improving ALS diagnosis.

Main Methods:

  • Review of current diagnostic modalities for ALS, including electrophysiology, genetic screening, spasticity scales, and MRI.
  • Assessment of the reliability, sensitivity, and specificity of these techniques.

Main Results:

  • Simplified electrophysiologic approaches are easy to perform but difficult to interpret in complex cases.

Related Experiment Videos

  • Genetic screening and MRI show potential but require further research due to limited patient data and specificity.
  • Spasticity scales are less effective for mild cases and at the early stages of diagnosis.
  • Conclusions:

    • The diagnostic approach for ALS requires enhancement, potentially by increasing the weight of electrophysiologic findings and rigorously excluding mimic disorders.
    • Improving the initial evaluation and suspicion of ALS is crucial, as current rates of suspicion are low (27-40%).
    • Further research is needed to validate new diagnostic techniques for routine clinical use in ALS diagnosis.