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Leda Volpi

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Articles 12
Citations 193
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Recent Articles
1.
Chiti A, Cecchi P, Pesaresi I, Orlandi G, Giannini N, Gialdini G, et al.
Psychiatry Res Neuroimaging . 2018 Dec; 282:126-131. PMID: 30539733
Leukoaraiosis is one of the main contributors to mild cognitive impairment due to vascular damage (vascular MCI, VMCI), whose pathophysiology has not been fully elucidated yet. We aimed to shed...
2.
Vergallo A, Giampietri L, Baldacci F, Volpi L, Chico L, Pagni C, et al.
Am J Alzheimers Dis Other Demen . 2017 Sep; 33(1):35-41. PMID: 28931301
Background: Oxidative stress (OS) is a physiological age-related brain process, dramatically overexpressed in neurodegenerative disorders like Alzheimer's disease (AD). Nevertheless, the pathophysiological role of OS in AD pathology has not...
3.
Volpi L, Pagni C, Radicchi C, Cintoli S, Miccoli M, Bonuccelli U, et al.
J Neurol Sci . 2017 May; 377:12-18. PMID: 28477679
No abstract available.
4.
Tonacci A, Bruno R, Ghiadoni L, Pratali L, Berardi N, Tognoni G, et al.
Eur J Neurosci . 2017 Apr; 45(10):1279-1288. PMID: 28370677
Mild Cognitive Impairment (MCI) is an intermediate condition between normal aging and dementia, associated with an increased risk of progression into the latter within months or years. Olfactory impairment, a...
5.
Baldanzi S, Bevilacqua F, Lorio R, Volpi L, Simoncini C, Petrucci A, et al.
Orphanet J Rare Dis . 2016 Apr; 11:34. PMID: 27044540
Background: Myotonic dystrophy type 1 (Steinert's disease or DM1), the most common form of autosomal dominant muscular dystrophy in adults, is a multisystem disorder, affecting skeletal muscle as well as...
6.
Maestri M, Carnicelli L, Tognoni G, Di Coscio E, Giorgi F, Volpi L, et al.
Sleep Med . 2015 Aug; 16(9):1139-45. PMID: 26298791
Objective: Polysomnographic (PSG) studies in mild cognitive impairment (MCI) are not conclusive and are limited only to conventional sleep parameters. The aim of our study was to evaluate sleep architecture...
7.
Ricci G, Scionti I, Ali G, Volpi L, Zampa V, Fanin M, et al.
Neuromuscul Disord . 2012 Jan; 22(6):534-40. PMID: 22245016
We report the first case of a heterozygous T78M mutation in the caveolin-3 gene (CAV3) associated with rippling muscle disease and proximal myopathy. The patient displayed also bilateral winged scapula...
8.
Tosetti M, Linsalata S, Battini R, Volpi L, Cini C, Presciutti O, et al.
Muscle Nerve . 2011 Sep; 44(5):816-9. PMID: 21952990
Although the molecular defect causing Becker muscular dystrophy (BMD) has been identified, the biochemical mechanisms that lead to muscle necrosis remain unclear. Exercise-related muscle metabolism in 9 mildly affected BMD...
9.
Mancuso M, Piazza S, Volpi L, Orsucci D, Calsolaro V, Caldarazzo Ienco E, et al.
Neurol Sci . 2011 Jul; 33(2):449-52. PMID: 21751099
Involvement of the peripheral nervous system in mitochondrial disorders (MD) has been previously reported. However, the exact prevalence of peripheral neuropathy and/or myopathy in MD is still unclear. In order...
10.
Franzini M, Fornaciari I, Siciliano G, Volpi L, Ricci G, Marchi S, et al.
Clin Biochem . 2010 Aug; 43(15):1246-8. PMID: 20691173
Objectives: Elevation of serum gamma-glutamyltransferase (GGT), in absence of a clinically significant liver damage, is often found in Myotonic Dystrophy type-1 (DM1). In this study we investigated if a specific...