4 results match your criteria: "AFaR-Fatebenefratelli Hospital "San Giovanni Calibita[Affiliation]"
Neurobiol Aging
September 2014
Department of Neuroscience, AFaR-Fatebenefratelli Hospital "San Giovanni Calibita," Rome, Italy; Laboratory of Neurodegeneration, Istituto Di Ricovero e Cura a Carattere Scientifico (IRCCS) San Raffaele Pisana, Rome, Italy.
Risk of developing Alzheimer's disease is increased by older age, genetic factors, and several medical risk factors. Studies have also suggested that dietary and lifestyle factors may influence risk, raising the possibility that preventive strategies may be effective. This body of research is incomplete.
View Article and Find Full Text PDFJ Alzheimers Dis
August 2014
Department of Neuroscience, AFaR - Fatebenefratelli Hospital "San Giovanni Calibita", Rome, Italy Laboratory of Neurodegeneration, IRCSS San Raffaele Pisana, Rome, Italy.
The fraction of copper not bound to ceruloplasmin seems altered in Alzheimer's disease (AD). We have addressed this notion evaluating all the studies carried out from 1996 until March 2013 by means of meta-analysis. We performed our analysis on diverse indices evaluating the relationship between copper and ceruloplasmin in general circulation, namely 'Non-Cp copper', '% Non-Cp copper', and 'Adjusted copper'.
View Article and Find Full Text PDFJ Alzheimers Dis
April 2014
Department of Neurology, "Campus Bio-Medico" University, Rome, Italy Department of Neuroscience, AFaR - Fatebenefratelli Hospital "San Giovanni Calibita", Rome, Italy.
Copper homeostasis abnormalities have been shown to be associated with Alzheimer's disease (AD), possibly by accelerating amyloid-β toxicity and plaque formation. The ATP7B gene plays a key role in controlling body copper balance. Our previous studies showed an association between ATP7B variants and AD risk.
View Article and Find Full Text PDFJ Endocrinol Invest
August 2005
Unit of Endocrinology, University of Roma Tor Vergata, AFaR Fatebenefratelli Hospital San Giovanni Calibita, Isola Tiberina, Italy.
The relevant age-related changes in male body composition are mainly related to the progressive decrease in the level of circulating anabolic hormones, among which testosterone (T) is rather important. Its decline, between the ages of 35 and 75, is associated to a loss of muscle mass and fibers number, a doubling of fat mass and a decrease in bone mineral density by 0.3% per yr after age 35; thus the relationship between age-related changes in body composition and T bioactivity reflects an important endocrine aspect of the aging male.
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