Roberto Gallassi
Overview
Explore the profile of Roberto Gallassi including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
25
Citations
488
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Stanzani-Maserati M, De Matteis M, Bosco L, Baccari F, Zenesini C, Mitolo M, et al.
Brain Sci
. 2024 Jun;
14(6).
PMID: 38928524
Background: This work aimed to study the Village Test (VT) in a group of patients with Alzheimer's disease (AD) and compare the results with those of a group of patients...
2.
Maserati M, Matacena M, Baccari F, Zenesini C, Gallassi R, Capellari S, et al.
Am J Alzheimers Dis Other Demen
. 2022 Nov;
37:15333175221129381.
PMID: 36317413
Objective: To study the evolution of the Tree Drawing Test (TDT) in a group of Alzheimer's disease (AD) patients. Methods: A total of 33 AD patients were consecutively evaluated by...
3.
Mitolo M, Stanzani-Maserati M, Capellari S, Testa C, Rucci P, Poda R, et al.
Neuroimage Clin
. 2019 May;
23:101843.
PMID: 31071594
This study investigated the ability of magnetic resonance spectroscopy (H-MRS) of posterior cingulate cortex (PCC) and brain volumetry to predict the progression from mild cognitive impairment (MCI) to Alzheimer's Disease...
4.
Guaraldi P, Poda R, Calandra-Buonaura G, Solieri L, Sambati L, Gallassi R, et al.
Neurology
. 2017 Nov;
89(20):2122.
PMID: 29133612
No abstract available.
5.
Terlizzi R, Calandra-Buonaura G, Zanigni S, Barletta G, Capellari S, Guaraldi P, et al.
Auton Neurosci
. 2016 Feb;
195:20-6.
PMID: 26896090
Background And Purpose: Adult-onset autosomal dominant leukodystrophy (ADLD) is a rare progressive neurological disorder caused by Lamin B1 duplication (LMNB1). Our aim was to investigate longitudinally the pattern of the...
6.
La Morgia C, Ross-Cisneros F, Koronyo Y, Hannibal J, Gallassi R, Cantalupo G, et al.
Ann Neurol
. 2015 Oct;
79(1):90-109.
PMID: 26505992
Objective: Melanopsin retinal ganglion cells (mRGCs) are photoreceptors driving circadian photoentrainment, and circadian dysfunction characterizes Alzheimer disease (AD). We investigated mRGCs in AD, hypothesizing that they contribute to circadian dysfunction....
7.
Zanigni S, Terlizzi R, Tonon C, Testa C, Manners D, Capellari S, et al.
Brain Res Bull
. 2015 Jul;
117:24-31.
PMID: 26189928
Introduction: adult-onset autosomal dominant leukodystrophy (ADLD) is a rare inherited disorder due to a duplication of lamin-B1 (LMNB1) gene. The aim of this study was to investigate brain metabolic and...
8.
Maserati M, Matacena C, Sambati L, Oppi F, Poda R, De Matteis M, et al.
Behav Neurol
. 2015 Jul;
2015:534681.
PMID: 26175548
Objective: To study the Tree-Drawing Test in a group of demented patients and compare it with a group of mild cognitively impaired patients (MCI) and controls. Methods: Consecutive outpatients were...
9.
Stanzani-Maserati M, Gallassi R, Calandra-Buonaura G, Alessandria M, Oppi F, Poda R, et al.
Eur Neurol
. 2014 Oct;
72(5-6):349-59.
PMID: 25322750
Background: The profile and degree of cognitive impairment in Multiple System Atrophy (MSA) and the impact of sleep disorders, REM sleep behavior disorder (RBD) in particular, in parkinsonism-related cognitive deficits...
10.
Guaraldi P, Poda R, Calandra-Buonaura G, Solieri L, Sambati L, Gallassi R, et al.
PLoS One
. 2014 Jan;
9(1):e85020.
PMID: 24465471
Objective: aims of the current study were 1) to evaluate global cognitive function in patients with autonomic failure (AF) of peripheral origin and 2) to investigate the effect of a...