Systemic amyloidosis is a rare protein misfolding and deposition disorder leading to
progressive organ failure. There are over 15 types of systemic amyloidosis, each caused by …

Amyloid A amyloidosis is thought to be the second most common form of systemic
amyloidosis behind amyloidosis secondary to monoclonal Ig. It is the result of deposition of …

Amyloid fibrils formed by the mis-aggregation of amyloid proteins can lead to neuronal
degenerations in the Alzheimer's disease. Predicting amyloid proteins not only contributes to …

DREAM (D p, R b-like, E 2F, a nd M uvB) is a transcriptional repressor complex that
regulates cell proliferation, and its loss causes neonatal lethality in mice. To investigate …

We present an extremely rare case of amyloid A (AA) deposition in the gallbladder and
review the literature on similar cases. The patient was a 76-year-old man who had been …

Objective: Herein, we aimed to evaluate the frequency and clinical features of AA
amyloidosis in patients with PsA followed up in our tertiary referral clinic. Methods: We …

Background Behcet's disease (BD) is a relapsing systemic vascular autoimmune/
inflammatory disease. Despite much effort to investigate BD, there are virtually no unique …

Objectives: Familial Mediterranean fever (FMF) is a monogenic auto-inflammatory disease
which might rarely cause glomerulopathy in patients. The aim of this study was to determine …

Objective The present study aims to evaluate the aetiology and clinicopathological profile of
renal amyloidosis, determine its various types, and their distribution within the kidney …

A Rare Case of Renal AA Amyloidosis Secondary to Sjogren’s Syndrome - PMC Back to Top
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