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

Multiple Sclerosis l: Introduction01:19

Multiple Sclerosis l: Introduction

Multiple sclerosis is a chronic autoimmune disease of the central nervous system (CNS) that affects the brain, spinal cord, and optic nerves. It is an inflammatory demyelinating disorder and a leading cause of neurological disability in young adults.EpidemiologyMS commonly begins between 20 and 40 years of age and is twice as common in women. Its exact cause remains unclear, but genetic susceptibility contributes, with higher risk in first-degree relatives and identical twins. A greater...
Myasthenia Gravis ll: Pathophysiology01:22

Myasthenia Gravis ll: Pathophysiology

The disease process of myasthenia gravis begins at the neuromuscular junction, where antibodies attack key proteins needed for muscle activation. This immune reaction weakens signal transmission, leading to the characteristic muscle fatigue and weakness that define the condition.Immune-Mediated DamageIn most individuals, antibodies target acetylcholine receptors (AChRs) on the postsynaptic membrane of muscle cells. By blocking acetylcholine binding, these antibodies prevent the nerve signal...
Secondary Spinal Cord Injury llI: Pathophysiology01:25

Secondary Spinal Cord Injury llI: Pathophysiology

Early Ischemia and Ionic ImbalanceWithin minutes of spinal cord injury, a secondary cascade begins, progressing over hours to weeks. Vascular damage reduces blood flow, causing ischemia and mitochondrial dysfunction. ATP depletion leads to ion pump failure, membrane depolarization, sodium influx, potassium efflux, and water accumulation, resulting in cellular swelling. Increased intracellular calcium further disrupts mitochondria and accelerates cellular injury.Excitotoxicity and Neuronal...
Myasthenia Gravis: Diagnostic Tests01:15

Myasthenia Gravis: Diagnostic Tests

Myasthenia gravis is an autoimmune condition affecting neuromuscular transmission, causing generalized weakness in skeletal muscles. Initial diagnoses rely on patients' signs, symptoms, and medical history. The challenge lies in distinguishing myasthenia from other muscular dystrophies. An important diagnostic feature is the significant improvement of symptoms after administering anticholinesterase inhibitors.
The edrophonium test is a diagnostic tool for myasthenia gravis. It involves...
Chemical Synapses01:26

Chemical Synapses

Chemical synapses are specialized sites between two neurons or between a neuron and a non-neuronal cell like a muscle, glandular or sensory cell.
Because chemical synapses depend on the release of neurotransmitter molecules from synaptic vesicles to pass on their signal, there is an approximately one millisecond delay between when the axon potential reaches the presynaptic terminal and when the neurotransmitter leads to opening of postsynaptic ion channels. Additionally, this signaling is...
Chemical Synapses01:26

Chemical Synapses

Chemical synapses are specialized sites between two neurons or between a neuron and a non-neuronal cell like a muscle, glandular or sensory cell.
Because chemical synapses depend on the release of neurotransmitter molecules from synaptic vesicles to pass on their signal, there is an approximately one millisecond delay between when the axon potential reaches the presynaptic terminal and when the neurotransmitter leads to opening of postsynaptic ion channels. Additionally, this signaling is...

You might also read

Related Articles

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

Sort by
Same author

Association of Plasma and Cerebrospinal Fluid Glucose Level with Clinical Severity in Patients with Guillain-Barre Syndrome.

Mymensingh medical journal : MMJ·2026
Same author

Assessment of Clinical Profile and Biochemical Parameters in Diverse Phenotypes of Polycystic Ovarian Syndrome.

Mymensingh medical journal : MMJ·2025
Same author

Antibody Level against Hepatitis B Virus in Term and Preterm Infants Following Three Doses of Pentavalent Vaccine as per EPI Schedule.

Mymensingh medical journal : MMJ·2025
Same author

Glycated Haemoglobin in Last Trimester Pregnancy as a Predictor of Neonatal Hypoglycaemia in Infants of Diabetic Mother.

Mymensingh medical journal : MMJ·2025
Same author

Comparative Study of Complications of Single-Tract versus Multi-Tract Percutaneous Nephrolithotomy Using the Modified Clavien System.

Mymensingh medical journal : MMJ·2025
Same author

Evaluation of Risk Factors Associated with Stillbirth in a Tertiary Level Hospital.

Mymensingh medical journal : MMJ·2025
Same journal

Non-secretory Multiple Myeloma: A Challenge to Diagnose.

Mymensingh medical journal : MMJ·2026
Same journal

Scrotal Cystocele with Right Inguinoscrotal Hernia: A Rare Case Report.

Mymensingh medical journal : MMJ·2026
Same journal

Treatment of Base of Condyle Fracture Using Minimal Access Surgery: Infinitesimal Peri-Angular Pterygomasseteric Transsectioning Approach (IPPTA): A Case Report.

Mymensingh medical journal : MMJ·2026
Same journal

BATH-PLUG Technique in Case of Endoscopic Management of Cerebrospinal Fluid Rhinorrhea.

Mymensingh medical journal : MMJ·2026
Same journal

A Six Year Old Boy with Lepromatous Leprosy: A Case Report Revealing an Unsolved Mystery.

Mymensingh medical journal : MMJ·2026
Same journal

The Correlation between Exposure to Screen Time and Severity of Autism Spectrum Disorder in Children in Bangladesh: A Case-Control Study.

Mymensingh medical journal : MMJ·2026
See all related articles

Related Experiment Video

Updated: May 27, 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

Guillian-Barre syndrome.

R K Talukder1, S R Sutradhar, K M Rahman

  • 1Mymensingh Medical College, Mymensingh, Bangladesh.

Mymensingh Medical Journal : MMJ
|November 15, 2011
PubMed
Summary
This summary is machine-generated.

Guillian-Barre syndrome (GBS), a cause of acute flaccid paralysis, is strongly linked to Campylobacter jejuni infection. Early diagnosis and treatment improve outcomes for this condition.

More Related Videos

Induction of Paralysis and Visual System Injury in Mice by T Cells Specific for Neuromyelitis Optica Autoantigen Aquaporin-4
09:29

Induction of Paralysis and Visual System Injury in Mice by T Cells Specific for Neuromyelitis Optica Autoantigen Aquaporin-4

Published on: August 21, 2017

A Protocol for Comprehensive Assessment of Bulbar Dysfunction in Amyotrophic Lateral Sclerosis (ALS)
12:43

A Protocol for Comprehensive Assessment of Bulbar Dysfunction in Amyotrophic Lateral Sclerosis (ALS)

Published on: February 21, 2011

Related Experiment Videos

Last Updated: May 27, 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

Induction of Paralysis and Visual System Injury in Mice by T Cells Specific for Neuromyelitis Optica Autoantigen Aquaporin-4
09:29

Induction of Paralysis and Visual System Injury in Mice by T Cells Specific for Neuromyelitis Optica Autoantigen Aquaporin-4

Published on: August 21, 2017

A Protocol for Comprehensive Assessment of Bulbar Dysfunction in Amyotrophic Lateral Sclerosis (ALS)
12:43

A Protocol for Comprehensive Assessment of Bulbar Dysfunction in Amyotrophic Lateral Sclerosis (ALS)

Published on: February 21, 2011

Area of Science:

  • Neurology
  • Infectious Diseases
  • Immunology

Background:

  • Guillian-Barre syndrome (GBS) is a primary cause of acute flaccid paralysis, affecting all age groups but more prevalent in the elderly.
  • Campylobacter jejuni, a common cause of bacterial gastroenteritis, is increasingly recognized as a frequent antecedent pathogen for GBS.
  • The pathogenesis involves molecular mimicry between microbial epitopes and gangliosides in the Schwann cell membrane.

Purpose of the Study:

  • To investigate the association between Campylobacter jejuni infection and Guillian-Barre syndrome.
  • To highlight the diagnostic and prognostic factors in GBS.
  • To discuss potential preventive strategies for GBS.

Main Methods:

  • A prospective case-controlled study design was employed.
  • Serological testing for C. jejuni was performed on GBS patients, family controls, and patients with other neurological diseases.
  • Clinical diagnosis, supportive care, plasma exchange, and intravenous immunoglobulin therapy were evaluated.

Main Results:

  • A high frequency (57%) of positive C. jejuni serology was observed in GBS patients, compared to 8% in family controls and 3% in other neurological disease controls.
  • Respiratory failure and autonomic dysfunction are identified as primary causes of mortality in GBS.
  • Prognosis is generally good, with 80% of patients achieving full recovery within 3-6 months, though 4% mortality and residual disability occur.

Conclusions:

  • Campylobacter jejuni is a significant antecedent pathogen in Guillian-Barre syndrome.
  • Supportive care, plasma exchange, and IVIg are crucial for managing GBS and improving outcomes.
  • Development of a C. jejuni vaccine could potentially prevent GBS, emphasizing the importance of early and specific diagnosis for favorable outcomes.