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

[Dysautonomia in acute primary polyradiculoneuritis].

M Goulon, F Nouailhat, P Babinet

    Revue Neurologique
    |February 1, 1975
    PubMed
    Summary

    This study on acute primary polyradiculoneuritis highlights frequent autonomic disorders, including circulatory issues and metabolic changes. These findings emphasize careful therapeutic approaches for patients with this neurological condition.

    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

    Core-rod myopathy caused by mutations in the nebulin gene.

    Neurology·2009
    Same author

    The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa.

    Neurology·2008
    Same author

    Tongue weakness is associated with respiratory failure in patients with severe Guillain-Barré syndrome.

    Acta neurologica Scandinavica·2008
    Same author

    Nocturnal mechanical ventilation for chronic hypoventilation in patients with neuromuscular and chest wall disorders.

    The Cochrane database of systematic reviews·2007
    Same author

    The G526R glycyl-tRNA synthetase gene mutation in distal hereditary motor neuropathy type V.

    Neurology·2006
    Same author

    A gene for an autosomal recessive lower motor neuron disease with childhood onset maps to 1p36.

    Neurology·2006

    Area of Science:

    • Neurology
    • Endocrinology
    • Internal Medicine

    Context:

    • Investigates autonomic dysfunction in 172 cases of acute primary polyradiculoneuritis.
    • Focuses on circulatory disorders (hypertension, bradycardia), water retention, and glucose metabolism abnormalities.

    Purpose:

    • To detail the frequency and severity of autonomic disorders in acute primary polyradiculoneuritis.
    • To explore correlations between specific biomarkers and clinical manifestations.
    • To provide therapeutic recommendations based on observed patterns.

    Summary:

    • Identified significant correlations between arterial hypertension and VMA/catecholamine levels, and hyperglycemia with urinary 17 OH levels.
    • Observed negative free water clearance that resolves with paralytic syndrome improvement, mimicking inappropriate antidiuretic hormone (HAD) secretion.

    Related Experiment Videos

  • Emphasizes the need for caution in therapeutic interventions and drug prescriptions for this condition.

    • Impact:

    • Enhances understanding of the complex autonomic and metabolic disturbances in acute primary polyradiculoneuritis.
    • Suggests potential diagnostic biomarkers for monitoring disease progression and severity.
    • Informs clinical practice by advising cautious therapeutic strategies to mitigate risks associated with autonomic dysfunction.