"Amyloidosis, Familial" 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.
Diseases in which there is a familial pattern of AMYLOIDOSIS.
| Descriptor ID |
D028226
|
| MeSH Number(s) |
C16.320.565.176 C18.452.648.176 C18.452.845.500.075
|
| Concept/Terms |
Amyloidosis, Familial- Amyloidosis, Familial
- Amyloidoses, Familial
- Familial Amyloidoses
- Familial Amyloidosis
- Amyloidosis, Hereditary
- Amyloidoses, Hereditary
- Hereditary Amyloidoses
- Hereditary Amyloidosis
|
Below are MeSH descriptors whose meaning is more general than "Amyloidosis, Familial".
Below are MeSH descriptors whose meaning is more specific than "Amyloidosis, Familial".
This graph shows the total number of publications written about "Amyloidosis, Familial" by people in this website by year, and whether "Amyloidosis, Familial" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2011 | 1 | 0 | 1 |
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Below are the most recent publications written about "Amyloidosis, Familial" by people in Profiles.
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Ueda M, Ageyama N, Nakamura S, Nakamura M, Chambers JK, Misumi Y, Mizuguchi M, Shinriki S, Kawahara S, Tasaki M, Jono H, Obayashi K, Sasaki E, Une Y, Ando Y. Aged vervet monkeys developing transthyretin amyloidosis with the human disease-causing Ile122 allele: a valid pathological model of the human disease. Lab Invest. 2012 Mar; 92(3):474-84.