Martina Gandola

Prof. Martina Gandola

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Research Focus & Metrics

Academic Career Length

22Years (2005-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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15 July 2005 in Science
Verified
Journal Article
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ABA. Berti
A. Berti
GBGabriella Bottini
Gabriella Bottini
MGMartina Gandola
Martina Gandola
LPLorenzo Pia
Lorenzo Pia
NSN. Smania
N. Smania
EPE. Paulesu
E. Paulesu
In everyday life, the successful monitoring of behavior requires continuous updating of the effectiveness of motor acts; one crucial step is becoming aware of the movements one is performing. We studied the anatomical distribution of lesions in right-brain–damaged hemiplegic patients, who obstinately denied their motor impairment, claiming that they could move their paralyzed limbs. Denial was associated with lesions in areas related to the programming of motor acts, particularly Brodmann's premotor areas 6 and 44, motor area 4, and the somatosensory cortex. This association suggests that monitoring systems may be implemented within the same cortical network that is responsible for the primary function that has to be monitored.

1 October 2012 in Cortex
Verified
Journal Article
Closed access
MGMartina Gandola
Martina Gandola
PIPaola Invernizzi
Paola Invernizzi
ASAnna Sedda
Anna Sedda
EFElisa R. Ferrè
Elisa R. Ferrè
RSRoberto Sterzi
Roberto Sterzi
GBGabriella Bottini
Gabriella Bottini

14 February 2014 in Brain
Verified
Journal Article
Open access
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DRDaniele Romano
Daniele Romano
MGMartina Gandola
Martina Gandola
GBGabriella Bottini
Gabriella Bottini
AMAngelo Maravita
Angelo Maravita
A complex brain representation of our body allows us to monitor incoming sensory stimuli and plan actions towards the external world. A critical element of such a complex representation is the sense of ownership towards our own body parts. Brain damage may disrupt this representation, leading to the striking neuropsychological condition called somatoparaphrenia, that is, the delusion that one’s own limbs belong to someone else. The clinical features characterizing somatoparaphrenia are well known, however, physiological clues of the level at which this condition may disrupt sensory functions are unknown. In the present study we investigated this issue by measuring the anticipatory skin conductance response to noxious stimuli approaching either the affected or the intact body side in a group of patients with somatoparaphrenia (n = 5; three females, age range = 66–84), and in a group of patients with anosognosia for sensory deficits, i.e. preserved ownership but decreased awareness of somatosensory deficit, (n = 5; one female, age range = 62–81 years) and in a group of purely hemiplegic patients (n = 5; two females, age range = 63–74 years) with no deficits of ownership or sensory awareness. Results show that anticipatory skin conductance responses to noxious stimuli directed to the contralesional hand are significantly reduced as compared to noxious stimuli directed to the ipsilesional hand in patients with somatoparaphrenia. By contrast a non-reduced anticipatory skin conductance response was observed in control participants as well as in patients affected by anosognosia for the somatosensory deficit and in patients affected by pure motor deficits. Furthermore, a pain anticipation response was always measured when the stimuli were directed towards the ipsilesional, unaffected hand in all groups. Our results show for the first time that the delusions shown by somatoparaphrenic patients are associated with an altered physiological index of perceptual analysis. The reduced response to sensory threats approaching the body suggests a deep detachment of the affected body part from the patient’s body representation. Conversely, normal reactions to incoming threats are found in the presence of impaired sensory awareness but intact body ownership, supporting the notion that representation of the body may be affected at different levels following brain damage.

25 October 2005 in Neurology
Verified
Journal Article
Closed access
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GBGabriella Bottini
Gabriella Bottini
EPE. Paulesu
E. Paulesu
MGMartina Gandola
Martina Gandola
SLS. Loffredo
S. Loffredo
PSP. Scarpa
P. Scarpa
GVG. Vallar
G. Vallar
Background: Left caloric vestibular stimulation (CVS) transiently reduces impairments of right-brain-damaged patients with left unilateral neglect, including left hemianesthesia, contralateral to the side of the lesion (contralesional). Conversely, no effect on right contralesional hemianesthesia in left-brain-damaged patients is seen with right CVS. This discrepancy is unexplained. Methods: The authors explored the effect of CVS on right- and left-brain-damaged patients with hemianesthesia. One left-brain-damaged patient had an fMRI study during tactile stimulation before and after left CVS. The same fMRI touch study, without CVS, was performed in neurologically unimpaired subjects. Results: A transient remission of right hemianesthesia associated with left brain damage was observed, provided that cold CVS was administered to the left ear. In the left-brain-damaged patient studied with fMRI, left CVS modulated the neural response to right hand tactile stimuli of a portion of the secondary somatosensory area (SII) of the right hemisphere. In neurologically unimpaired subjects, fMRI scans showed that the same part of area SII in the right hemisphere was activated by ipsilateral right-sided touches and to a larger extent than area SII in the left hemisphere by left-sided touches. Conclusions: Left caloric vestibular stimulation is effective on both left and right hemianesthesia because it modulates the hemisphere that has a more complete representation of, or is capable to attend to, the whole somatosensory surface of the body. These results suggest a hardwired hemispheric asymmetry in hand representation, starting from a somatotopically organized brain region such as area SII.

25 November 2012 in Experimental Brain Research
Verified
Journal Article
Closed access
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LZLaura Zapparoli
Laura Zapparoli
PIP. Invernizzi
P. Invernizzi
MGMartina Gandola
Martina Gandola
MVM. Verardi
M. Verardi
MBManuela Berlingeri
Manuela Berlingeri
EPE. Paulesu
E. Paulesu

24 August 2014 in Experimental Brain Research
Verified
Journal Article
Closed access
PDF file
LZLaura Zapparoli
Laura Zapparoli
PIPaola Invernizzi
Paola Invernizzi
MGMartina Gandola
Martina Gandola
MBManuela Berlingeri
Manuela Berlingeri
ASAntonio De Santis
Antonio De Santis
EPEraldo Paulesu
Eraldo Paulesu