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 Concept Videos

Somatosensation01:33

Somatosensation

The somatosensory system relays sensory information from the skin, mucous membranes, limbs, and joints. Somatosensation is more familiarly known as the sense of touch. A typical somatosensory pathway includes three types of long neurons: primary, secondary, and tertiary. Primary neurons have cell bodies located near the spinal cord in groups of neurons called dorsal root ganglia. The sensory neurons of ganglia innervate designated areas of skin called dermatomes.
Psychosis: Pathophysiology of Schizophrenia and Other Psychotic Disorders01:27

Psychosis: Pathophysiology of Schizophrenia and Other Psychotic Disorders

Schizophrenia is a neurodevelopmental disorder whose origins are rooted in complex genetic components. Despite our burgeoning understanding, the pathophysiology of this disorder remains incompletely deciphered.
Researchers have identified genetic factors that increase susceptibility to schizophrenia, underscoring the intricate interplay between genetics and environment in disease development. At the core of schizophrenia's pathophysiology is excessive dopaminergic neurotransmission within the...

You might also read

Related Articles

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

Sort by
Same author

Chronic inflammatory demyelinating polyradiculoneuropathy-associated tremor: Phenotype and pathogenesis.

European journal of neurology·2023
Same author

Multiple pathways of lipid dysregulation in amyotrophic lateral sclerosis.

Brain communications·2023
Same author

Consensus for experimental design in electromyography (CEDE) project: Single motor unit matrix.

Journal of electromyography and kinesiology : official journal of the International Society of Electrophysiological Kinesiology·2022
Same author

Riluzole is associated with decreasing neuritic plaque severity in amyotrophic lateral sclerosis.

Brain : a journal of neurology·2022
Same author

Progress, development, and challenges in amyotrophic lateral sclerosis clinical trials.

Expert review of neurotherapeutics·2022
Same author

Distinct hypothalamic involvement in the amyotrophic lateral sclerosis-frontotemporal dementia spectrum.

NeuroImage. Clinical·2022

Related Experiment Video

Updated: May 7, 2026

Utility of Dissociated Intrinsic Hand Muscle Atrophy in the Diagnosis of Amyotrophic Lateral Sclerosis
08:16

Utility of Dissociated Intrinsic Hand Muscle Atrophy in the Diagnosis of Amyotrophic Lateral Sclerosis

Published on: March 4, 2014

ALS pathophysiology: insights from the split-hand phenomenon.

Parvathi Menon1, Matthew C Kiernan2, Steve Vucic3

  • 1Sydney Medical School Westmead, University of Sydney, Sydney, Australia.

Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|September 21, 2013
PubMed
Summary
This summary is machine-generated.

Amyotrophic lateral sclerosis (ALS) shows a reduced split-hand index, indicating preferential muscle atrophy. Peripheral axonal dysfunction is unlikely to be the primary cause of split-hand in ALS.

Keywords:
ALSAxonal excitabilitySplit-hand

More Related Videos

Block Building Task Identifies Distinct Groups of Left/Right-hand Choice Patterns After Unilateral Peripheral Nerve Injury
07:06

Block Building Task Identifies Distinct Groups of Left/Right-hand Choice Patterns After Unilateral Peripheral Nerve Injury

Published on: March 21, 2025

Related Experiment Videos

Last Updated: May 7, 2026

Utility of Dissociated Intrinsic Hand Muscle Atrophy in the Diagnosis of Amyotrophic Lateral Sclerosis
08:16

Utility of Dissociated Intrinsic Hand Muscle Atrophy in the Diagnosis of Amyotrophic Lateral Sclerosis

Published on: March 4, 2014

Block Building Task Identifies Distinct Groups of Left/Right-hand Choice Patterns After Unilateral Peripheral Nerve Injury
07:06

Block Building Task Identifies Distinct Groups of Left/Right-hand Choice Patterns After Unilateral Peripheral Nerve Injury

Published on: March 21, 2025

Area of Science:

  • Neuroscience
  • Neurology

Background:

  • Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease.
  • The split-hand phenomenon, characterized by preferential atrophy of intrinsic hand muscles, is a common feature in ALS.
  • The underlying mechanisms contributing to split-hand in ALS are not fully understood.

Purpose of the Study:

  • To investigate the role of peripheral axonal dysfunction in the development of split-hand in ALS patients.
  • To assess whether peripheral nerve excitability changes correlate with the split-hand phenomenon in ALS.

Main Methods:

  • Motor axonal excitability studies of median and ulnar nerves were performed on 21 ALS patients and 24 controls.
  • Measurements included abductor pollicis brevis (APB), abductor digit minimi (ADM), and first dorsal interosseous (FDI) muscle responses.
  • The split-hand index (SI) was calculated as a biomarker of muscle atrophy.

Main Results:

  • ALS patients exhibited a significantly reduced split-hand index compared to controls (P<0.0001).
  • Axonal excitability studies revealed prolonged strength-duration time constants in APB and ADM axons in ALS patients.
  • Increased depolarizing threshold electrotonus and superexcitability were observed in APB and FDI axons.

Conclusions:

  • The findings reinforce the significance of the split-hand phenomenon in ALS.
  • Peripheral axonal dysfunction does not appear to be a primary contributor to split-hand development in ALS.
  • Observed axonal dysfunction may be a secondary downstream effect of ALS pathophysiology.