Search Results - "Grisoli, M."

White matter involvement in idiopathic Parkinson disease: a diffusion tensor imaging study by Gattellaro, G, Minati, L, Grisoli, M, Mariani, C, Carella, F, Osio, M, Ciceri, E, Albanese, A, Bruzzone, M G

“…Diffusion tensor imaging (DTI) offers a unique window on the connectivity changes, extending beyond the basal ganglia, which accompany the cognitive symptoms…”
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Diffusion Tensor Imaging Shows Different Topographic Involvement of the Thalamus in Progressive Supranuclear Palsy and Corticobasal Degeneration by Erbetta, A, Mandelli, M.L, Savoiardo, M, Grisoli, M, Bizzi, A, Soliveri, P, Chiapparini, L, Prioni, S, Bruzzone, M.G, Girotti, F

“…In progressive supranuclear palsy (PSP) and corticobasal degeneration (CBD), postmortem studies show different topographic involvement of the thalamus, basal…”
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Supratentorial and pontine MRI abnormalities characterize recessive spastic ataxia of Charlevoix-Saguenay. A comprehensive study of an Italian series by Prodi, E., Grisoli, M., Panzeri, M., Minati, L., Fattori, F., Erbetta, A., Uziel, G., D'Arrigo, S., Tessa, A., Ciano, C., Santorelli, F. M., Savoiardo, M., Mariotti, C.

“…Background and purpose The autosomal recessive spastic ataxia of Charlevoix‐Saguenay (ARSACS) is an early‐onset neurodegenerative disorder caused by mutations…”
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Advanced MRI may complement histological diagnosis of lower grade gliomas and help in predicting survival by Cuccarini, Valeria, Erbetta, A., Farinotti, M., Cuppini, L., Ghielmetti, F., Pollo, B., Di Meco, F., Grisoli, M., Filippini, G., Finocchiaro, G., Bruzzone, M. G., Eoli, M.

“…MRI grading of grade II and III gliomas may have an important impact on treatment decisions. Occasionally, both conventional MRI (cMRI) and histology fail to…”
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MR Spectroscopy, Functional MRI, and Diffusion-Tensor Imaging in the Aging Brain: A Conceptual Review by Minati, L., Grisoli, M., Bruzzone, M. G.

“…In vivo magnetic resonance spectroscopy (MRS), functional magnetic resonance imaging (fMRI), and diffusion-tensor imaging (DTI) have recently opened new…”
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Further in-depth look at superficial siderosis (and intracranial hypotension) by Savoiardo, M, Grisoli, M

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Imaging Degeneration of the Substantia Nigra in Parkinson Disease with Inversion-Recovery MR Imaging by Minati, L, Grisoli, M, Carella, F, De Simone, T, Bruzzone, M.G, Savoiardo, M

“…Visualizing with MR imaging and obtaining quantitative indexes of degeneration of the substantia nigra in Parkinson disease have been long-sought goals. We…”
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Diffusion Tensor Imaging of Spinocerebellar Ataxias Types 1 and 2 by Mandelli, M.L, De Simone, T, Minati, L, Bruzzone, M.G, Mariotti, C, Fancellu, R, Savoiardo, M, Grisoli, M

“…Structural MR imaging does not enable reliable differentiation of spinocerebellar ataxia (SCA) types 1 and 2 (SCA1 and SCA2), and imaging may be normal during…”
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Pendular nystagmus in progressive ataxia and palatal tremor by Bassani, R., Mariotti, C., Nanetti, L., Grisoli, M., Savoiardo, M., Pareyson, D., Salsano, E.

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Spinocerebellar ataxia type 17 (SCA17) : Oculomotor phenotype and clinical characterization of 15 Italian patients by MARIOTTI, Caterina, ALPINI, Dario, TARONI, Franco, GELLERA, Cinzia, DI DONATO, Stefano, FANCELLU, Roberto, SOLIVERI, Paola, GRISOLI, Marina, RAVAGLIA, Sabrina, LOVATI, Carlo, FETONI, Vincenza, GIACCONE, Giorgio, CASTUCCI, Alessia

“…SCA17 is a rare type of autosomal dominant spinocerebellar ataxia caused by a CAG/CAA expansion in the gene encoding the TATA-binding protein (TBP). We…”
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Decreased Diffusivity in the Caudate Nucleus of Presymptomatic Huntington Disease Gene Carriers: Which Explanation? by MANDELLI, M. L, SAVOIARDO, M, MINATI, L, MARIOTTI, C, AQUINO, D, ERBETTA, A, GENITRINI, S, DI DONATO, S, BRUZZONE, M. G, GRISOLI, M

“…The neostriatum is known to be affected in HD. In this work, our aim was to determine whether microstructural and volumetric alterations occur in the…”
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Iron chelation therapy in aceruloplasminaemia: study of a patient with a novel missense mutation by Mariani, R, Arosio, C, Pelucchi, S, Grisoli, M, Piga, A, Trombini, P, Piperno, A

“…We describe a novel missense mutation of ceruloplasmin in a patient with aceruloplasminaemia causing the replacement of a neutral amino acid (phenylalanine)…”
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Cognitive and magnetic resonance imaging aspects of corticobasal degeneration and progressive supranuclear palsy by SOLIVERI, P, MONZA, D, PARIDI, D, RADICE, D, GRISOLI, M, TESTA, D, SAVOIARDO, M, GIROTTI, F

“…To identify cognitive and MRI features important for the clinical diagnosis of corticobasal degeneration (CBD) and progressive supranuclear palsy (PSP); these…”
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Superficial siderosis of the CNS: selective central myelin vulnerability and peripheral myelin sparing demonstrated by MRI by Grisoli, M., Maccagnano, E., De Simone, T., Savoiardo, M.

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Dendritic cells pulsed with glioma lysates induce immunity against syngeneic intracranial gliomas and increase survival of tumor-bearing mice by Pellegatta, S., Poliani, P. L., Corno, D., Grisoli, M., Cusimano, M., Ubiali, F., Baggi, F., Bruzzone, M. G., Finocchiaro, G.

“…In recent years, the use of dendritic cells (DC), the most powerful antigen presenting cells, has been proposed for the creation of vaccines against gliomas…”
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Imaging dementias by Savoiardo, M, Grisoli, M

“…Dementia is the progressive loss of intellectual functions due to involvement of cortical or subcortical areas. Specific involvement of certain brain areas in…”
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Pathogenic effect of an intermediate-size SCA-6 allele (CAG)19 in a homozygous patient by MARIOTTI, C, GELLERA, C, GRISOLI, M, MINERI, R, CASTUCCI, A, DI DONATO, S

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White Matter Involvement in Idiopathic Parkinson Disease: A Diffusion Tensor Imaging Study by Gattellaro, G, Minati, L, Grisoli, M, Mariani, C, Carella, F, Osio, M, Ciceri, E, Albanese, A, Bruzzone, M.G

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Neuroradiological features of vertigo by Bruzzone, M G, Grisoli, M, De Simone, T, Regna-Gladin, C

“…The diagnostic pathway in a patient with vertigo starts with the accurate evaluation of medical history followed by a general physical and neurological…”
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A novel phenotype of sporadic Creutzfeldt–Jakob disease by Giaccone, G, Di Fede, G, Mangieri, M, Limido, L, Capobianco, R, Suardi, S, Grisoli, M, Binelli, S, Fociani, P, Bugiani, O, Tagliavini, F

“…An atypical case of sporadic Creutzfeldt–Jakob disease (CJD) is described in a 78-year-old woman homozygous for methionine at codon 129 of the prion protein…”
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