"Amyloid Neuropathies" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Disorders of the peripheral nervous system associated with the deposition of AMYLOID in nerve tissue. Familial, primary (nonfamilial), and secondary forms have been described. Some familial subtypes demonstrate an autosomal dominant pattern of inheritance. Clinical manifestations include sensory loss, mild weakness, autonomic dysfunction, and CARPAL TUNNEL SYNDROME. (Adams et al., Principles of Neurology, 6th ed, p1349)
Descriptor ID |
D017772
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MeSH Number(s) |
C10.668.829.050 C18.452.845.500.050
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Concept/Terms |
Amyloid Neuropathies- Amyloid Neuropathies
- Amyloid Polyneuropathies
- Amyloid Polyneuropathy
- Polyneuropathies, Amyloid
- Polyneuropathy, Amyloid
- Neuropathies, Amyloid
- Amyloid Neuropathy
- Neuropathy, Amyloid
Amyloid Neuropathy, Secondary- Amyloid Neuropathy, Secondary
- Amyloid Neuropathies, Secondary
- Neuropathies, Secondary Amyloid
- Neuropathy, Secondary Amyloid
- Secondary Amyloid Neuropathies
- Secondary Amyloid Neuropathy
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Below are MeSH descriptors whose meaning is more general than "Amyloid Neuropathies".
Below are MeSH descriptors whose meaning is more specific than "Amyloid Neuropathies".
This graph shows the total number of publications written about "Amyloid Neuropathies" by people in this website by year, and whether "Amyloid Neuropathies" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2019 | 1 | 0 | 1 |
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Below are the most recent publications written about "Amyloid Neuropathies" by people in Profiles.
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Sex-specific effects of microbiome perturbations on cerebral Aß amyloidosis and microglia phenotypes. J Exp Med. 2019 07 01; 216(7):1542-1560.
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Aged non-human primates: an animal model of age-associated neurodegenerative disease. Brain Pathol. 1991 Jul; 1(4):287-96.