Browsing by Author "Pievani, Michela (24476859800)"
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Publication Diffusion tensor MRI contributes to differentiate Richardson's syndrome from PSP-parkinsonism(2012) ;Agosta, Federica (6701687853) ;Pievani, Michela (24476859800) ;Svetel, Marina (6701477867) ;Ječmenica Lukić, Milica (35801126700) ;Copetti, Massimiliano (24474249000) ;Tomić, Aleksandra (26654535200) ;Scarale, Antonio (57204024869) ;Longoni, Giulia (37070849300) ;Comi, Giancarlo (7201788288) ;Kostić, Vladimir S. (57189017751)Filippi, Massimo (7202268530)This study investigated the regional distribution of white matter (WM) damage in Richardson's syndrome (PSP-RS) and progressive supranuclear palsy-Parkinsonism (PSP-P) using diffusion tensor (DT) magnetic resonance imaging (MRI). The DT MRI classificatory ability in diagnosing progressive supranuclear palsy (PSP) syndromes, when used in combination with infratentorial volumetry, was also quantified. In 37 PSP (21 PSP-RS, 16 PSP-P) and 42 controls, the program Tract-Based Spatial Statistics (TBSS; www.fmrib.ox.ac.uk/fsl/tbss) was applied. DT MRI metrics were derived from supratentorial, thalamic, and infratentorial tracts. The magnetic resonance parkinsonism index (MRPI) was calculated. All PSP harbored diffusivity abnormalities in the corpus callosum, frontoparietal, and frontotemporo-occipital tracts. Infratentorial WM and thalamic radiations were severely affected in PSP-RS and relatively spared in PSP-P. When MRPI and DT MRI measures were combined, the discriminatory power increased for each comparison. Distinct patterns of WM alterations occur in PSP-RS and PSP-P. Adding DT MRI measures to MRPI improves the diagnostic accuracy in differentiating each PSP syndrome from healthy individuals and each other. © 2012 Elsevier Inc.. - Some of the metrics are blocked by yourconsent settings
Publication Diffusion tensor MRI contributes to differentiate Richardson's syndrome from PSP-parkinsonism(2012) ;Agosta, Federica (6701687853) ;Pievani, Michela (24476859800) ;Svetel, Marina (6701477867) ;Ječmenica Lukić, Milica (35801126700) ;Copetti, Massimiliano (24474249000) ;Tomić, Aleksandra (26654535200) ;Scarale, Antonio (57204024869) ;Longoni, Giulia (37070849300) ;Comi, Giancarlo (7201788288) ;Kostić, Vladimir S. (57189017751)Filippi, Massimo (7202268530)This study investigated the regional distribution of white matter (WM) damage in Richardson's syndrome (PSP-RS) and progressive supranuclear palsy-Parkinsonism (PSP-P) using diffusion tensor (DT) magnetic resonance imaging (MRI). The DT MRI classificatory ability in diagnosing progressive supranuclear palsy (PSP) syndromes, when used in combination with infratentorial volumetry, was also quantified. In 37 PSP (21 PSP-RS, 16 PSP-P) and 42 controls, the program Tract-Based Spatial Statistics (TBSS; www.fmrib.ox.ac.uk/fsl/tbss) was applied. DT MRI metrics were derived from supratentorial, thalamic, and infratentorial tracts. The magnetic resonance parkinsonism index (MRPI) was calculated. All PSP harbored diffusivity abnormalities in the corpus callosum, frontoparietal, and frontotemporo-occipital tracts. Infratentorial WM and thalamic radiations were severely affected in PSP-RS and relatively spared in PSP-P. When MRPI and DT MRI measures were combined, the discriminatory power increased for each comparison. Distinct patterns of WM alterations occur in PSP-RS and PSP-P. Adding DT MRI measures to MRPI improves the diagnostic accuracy in differentiating each PSP syndrome from healthy individuals and each other. © 2012 Elsevier Inc.. - Some of the metrics are blocked by yourconsent settings
Publication The topography of brain damage at different stages of parkinson's disease(2013) ;Agosta, Federica (6701687853) ;Canu, Elisa (25225458900) ;Stojković, Tanja (57211211787) ;Pievani, Michela (24476859800) ;Tomić, Aleksandra (26654535200) ;Sarro, Lidia (38562146800) ;Dragašević, Nataša (59157743200) ;Copetti, Massimiliano (24474249000) ;Comi, Giancarlo (7201788288) ;Kostić, Vladimir S. (57189017751)Filippi, Massimo (7202268530)This study investigated gray matter (GM) and white matter (WM) damage in 89 patients at different clinical stages of Parkinson's disease (PD) (17 early, 46 mild, 14 moderate, and 12 severe) to differentiate the trajectories of tissue injury in this condition. PD patients had a very little GM atrophy even at the more advanced stages of the disease. Microstructural damage to the WM occurs with increasing PD severity and involves the brainstem, thalamocortical pathways, olfactory tracts, as well as the major interhemispheric, limbic, and extramotor association tracts. The most marked WM damage was found in moderate vs. mild cases. WM damage correlated with the degree of global cognitive deficits. WM abnormalities beyond the nigrostriatal system accumulate with increasing PD severity. WM damage is likely to contribute to the more severe motor and nonmotor dysfunctions occurring in patients at the later stages. © 2012 Wiley Periodicals, Inc. - Some of the metrics are blocked by yourconsent settings
Publication The topography of brain damage at different stages of parkinson's disease(2013) ;Agosta, Federica (6701687853) ;Canu, Elisa (25225458900) ;Stojković, Tanja (57211211787) ;Pievani, Michela (24476859800) ;Tomić, Aleksandra (26654535200) ;Sarro, Lidia (38562146800) ;Dragašević, Nataša (59157743200) ;Copetti, Massimiliano (24474249000) ;Comi, Giancarlo (7201788288) ;Kostić, Vladimir S. (57189017751)Filippi, Massimo (7202268530)This study investigated gray matter (GM) and white matter (WM) damage in 89 patients at different clinical stages of Parkinson's disease (PD) (17 early, 46 mild, 14 moderate, and 12 severe) to differentiate the trajectories of tissue injury in this condition. PD patients had a very little GM atrophy even at the more advanced stages of the disease. Microstructural damage to the WM occurs with increasing PD severity and involves the brainstem, thalamocortical pathways, olfactory tracts, as well as the major interhemispheric, limbic, and extramotor association tracts. The most marked WM damage was found in moderate vs. mild cases. WM damage correlated with the degree of global cognitive deficits. WM abnormalities beyond the nigrostriatal system accumulate with increasing PD severity. WM damage is likely to contribute to the more severe motor and nonmotor dysfunctions occurring in patients at the later stages. © 2012 Wiley Periodicals, Inc.
