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

Amyloid-related neuropathies.

H H Goebel1, J Bohl, S Störkel

  • 1Division of Neuropathology, University of Mainz, FRG.

Zentralblatt Fur Allgemeine Pathologie U. Pathologische Anatomie
|January 1, 1990
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

Neuronal ceroid lipofuscinosis (NCL) is caused by the entire deletion of CLN8 in the Alpenländische Dachsbracke dog.

Molecular genetics and metabolism·2016
Same author

Involvement of the cholinergic basal forebrain nuclei in spinocerebellar ataxia type 2 (SCA2).

Neuropathology and applied neurobiology·2013
Same author

Spinocerebellar ataxia type 1 (SCA1): new pathoanatomical and clinico-pathological insights.

Neuropathology and applied neurobiology·2012
Same author

Protein aggregation in inclusion body myositis, a sporadic form among protein aggregate myopathies, and in myofibrillar myopathies--a comparative study.

Romanian journal of internal medicine = Revue roumaine de medecine interne·2011
Same author

Psychic stress as a trigger of the spontaneous development and rupture of an aneurysm? A case report.

Interventional neuroradiology : journal of peritherapeutic neuroradiology, surgical procedures and related neurosciences·2010
Same author

Familial reducing body myopathy with cytoplasmic bodies and rigid spine revisited: identification of a second LIM domain mutation in FHL1.

Neuropediatrics·2010

Amyloid deposition in peripheral nerves causes amyloid-related neuropathies, often linked to myeloma or familial forms. Accurate amyloid typing via advanced techniques is crucial for precise diagnosis and management of these nerve disorders.

Area of Science:

  • Neurology
  • Pathology
  • Genetics

Background:

  • Amyloid-related neuropathies result from amyloid deposition in peripheral nerves.
  • These neuropathies can stem from myeloma-associated amyloid (AL) or familial amyloid polyneuropathy (AF) involving transthyretin variants.
  • Neuropathy is a key feature in systemic amyloidoses.

Purpose of the Study:

  • To highlight the importance of identifying amyloid types in neuropathies.
  • To emphasize the diagnostic value of histochemical and immunohistochemical techniques.
  • To underscore the necessity of searching for amyloid in adult neuropathies.

Main Methods:

  • Utilizing refined histochemical techniques.
  • Employing recent immunohistochemical methods.

Related Experiment Videos

  • Examining biopsied nerve specimens.
  • Main Results:

    • Accurate amyloid typing distinguishes between different forms of amyloid-related neuropathy.
    • Advanced techniques enable precise identification of amyloid subtypes.
    • Amyloid detection is critical for diagnosing specific neuropathies.

    Conclusions:

    • Precise identification of amyloid types is essential for accurate nosological classification of neuropathies.
    • The search for amyloid should be mandatory in adult neuropathies due to diverse causative factors.
    • Advanced diagnostic methods improve the understanding and management of amyloid-related nerve disorders.