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Amyloidosis, Familial

Known as: amyloidosis familial, Familial Amyloidoses, Familial Amyloidosis 
Diseases in which there is a familial pattern of AMYLOIDOSIS.
National Institutes of Health

Papers overview

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2016
2016
Background:  Primary localized cutaneous amyloidosis is a commonly encountered problem in our scenario. As there is paucity of… 
2011
2011
Amyloidosis refers to a group of protein misfolding diseases characterized by deposition of a particular amyloid protein in… 
2003
2003
A 38-year-old woman suffered from fatigue, stress-induced dyspnea, and a chronic cough. She also was suffering from loss of body… 
Review
2000
Review
2000
Systemic amyloidosis is a condition characterized by the extracellular deposition of insoluble fibrillar proteins, leading to… 
1985
1985
In a series of 13 elderly patients with proven prealbumin-related senile systemic amyloidosis (SSA), depressed serum prealbumin… 
1985
1985
In 106 patients with systemic amyloidosis (56 primary, 27 secondary, and 23 familial), serum amyloid A protein (SAA) was measured… 
1983
1983
Nine patients from 2 distinct kindreds with familial amyloidosis had episodes of inflammatory arthritis and radiographic evidence… 
1983
1983
Familial Amyloidosis with Polyneuropathy was first recognized in Portugal and reported by Andrade in 1952. The disease is rare… 
1981
1981
We report the M-mode and two-dimensional echocardiographic findings in a patient with familial amyloidosis. The diagnosis was… 
1969
1969
The observed incidence of ocular amyloid is to some extent a function of the diligence with which it is sought, recent reports…