Search Results - "DOTTI, Maria T"

Neurophthalmologic and Orthoptic Ambulatory Assessments Reveal Ocular and Visual Changes in Patients With Early Alzheimer and Parkinson's Disease by Bargagli, Alessia, Fontanelli, Enrica, Zanca, Dario, Castelli, Ilaria, Rosini, Francesca, Maddii, Silvia, Di Donato, Ilaria, Carluccio, Alessandra, Battisti, Carla, Tosi, Gian M., Dotti, Maria T., Rufa, Alessandra

“…Patients with Alzheimer's disease (AD) and Parkinson's disease (PD) develop a progressive decline of visual function. This condition aggravates overall…”
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Visual System Involvement in CADASIL by Pretegiani, Elena, MD, Rosini, Francesca, MD, Dotti, Maria T., MD, Bianchi, Silvia, PhD, Federico, Antonio, MD, Rufa, Alessandra, MD, PhD

“…Background and objective Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a hereditary arteriolar…”
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The role of dentate nuclei in human oculomotor control: insights from cerebrotendinous xanthomatosis by Rosini, Francesca, Pretegiani, Elena, Mignarri, Andrea, Optican, Lance M., Serchi, Valeria, Stefano, Nicola, Battaglini, Marco, Monti, Lucia, Dotti, Maria T., Federico, Antonio, Rufa, Alessandra

“…Key points A cerebellar dentate nuclei (DN) contribution to volitional oculomotor control has recently been hypothesized but not fully understood…”
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Postpartum psychiatric disturbances as an unrecognized onset of CADASIL by Pantoni, Leonardo, Pescini, Francesca, Inzitari, Domenico, T. Dotti, Maria

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APOE 2 is associated with white matter hyperintensity volume in CADASIL by Gesierich, Benno, Opherk, Christian, Rosand, Jonathan, Gonik, Mariya, Malik, Rainer, Jouvent, Eric, Herve, Dominique, Adib-Samii, Poneh, Bevan, Steve, Pianese, Luigi, Silvestri, Serena, Dotti, Maria T, De Stefano, Nicola, van der Grond, Jeroen, Boon, Elles M J, Pescini, Francesca, Rost, Natalia, Pantoni, Leonardo, Lesnik Oberstein, Saskia A, Federico, Antonio, Ragno, Michele, Markus, Hugh S, Tournier-Lasserve, Elisabeth, Chabriat, Hugues, Dichgans, Martin, Duering, Marco, Ewers, Michael

“…Apolipoprotein E ( APOE ) increases the risk for Alzheimer's disease ( 4 allele) and cerebral amyloid angiopathy ( 2 and 4), but its role in small vessel…”
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Differences in saccade dynamics between spinocerebellar ataxia 2 and late-onset cerebellar ataxias by FEDERIGHI, Pamela, CEVENINI, Gabriele, DOTTI, Maria T, ROSINI, Francesca, PRETEGIANI, Elena, FEDERICO, Antonio, RUFA, Alessandra

“…The cerebellum is implicated in maintaining the saccadic subsystem efficient for vision by minimizing movement inaccuracy and by learning from endpoint errors…”
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Eye movement changes in mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) by Vinciguerra, Claudia, Federighi, Pamela, Rosini, Francesca, Pretegiani, Elena, Cardaioli, Elena, Dotti, Maria T, Sicurelli, Francesco, Federico, Antonio, Rufa, Alessandra

“…Highlights • Describe the difference in eye movement characteristics in MNGIE. • Discuss about the extraocular muscles dependence to mitochondrial metabolism…”
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Sonographic and electrodiagnostic features of hereditary neuropathy with liability to pressure palsies by Ginanneschi, Federica, Filippou, Georgios, Giannini, Fabio, Carluccio, Maria A., Adinolfi, Antonella, Frediani, Bruno, Dotti, Maria T., Rossi, Alessandro

“…In hereditary neuropathy with liability to pressure palsies (HNPP), the increase in distal motor latencies (DMLs) is often out of proportion to the slowing of…”
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Bone Marrow-Derived Progenitor Cells in Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy by PESCINI, Francesca, CESARI, Francesca, GANDOLFO, Carlo, GORI, Anna M, ABBATE, Rosanna, PANTONI, Leonardo, INZITARI, Domenico, GIUSTI, Betti, SARTI, Cristina, ZICARI, Enza, BIANCHI, Silvia, DOTTI, Maria T, FEDERICO, Antonio, BALESTRINO, Maurizio, ENRICO, Adriano

“…Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is an inherited disease due to cerebral microangiopathy…”
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APOE ɛ2 is associated with white matter hyperintensity volume in CADASIL by Gesierich, Benno, Opherk, Christian, Rosand, Jonathan, Gonik, Mariya, Malik, Rainer, Jouvent, Eric, Hervé, Dominique, Adib-Samii, Poneh, Bevan, Steve, Pianese, Luigi, Silvestri, Serena, Dotti, Maria T, De Stefano, Nicola, van der Grond, Jeroen, Boon, Elles M J, Pescini, Francesca, Rost, Natalia, Pantoni, Leonardo, Lesnik Oberstein, Saskia A, Federico, Antonio, Ragno, Michele, Markus, Hugh S, Tournier-Lasserve, Elisabeth, Chabriat, Hugues, Dichgans, Martin, Duering, Marco, Ewers, Michael

“…Apolipoprotein E (APOE) increases the risk for Alzheimer’s disease (ɛ4 allele) and cerebral amyloid angiopathy (ɛ2 and ɛ4), but its role in small vessel…”
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Hand muscles corticomotor excitability in hereditary spastic paraparesis type 4 by Ginanneschi, Federica, Carluccio, Maria A., Mignarri, Andrea, Tessa, Alessandra, Santorelli, Filippo M., Rossi, Alessandro, Federico, Antonio, Dotti, Maria T.

“…Transcranial magnetic stimulation (TMS) studies on the pathways to the upper limbs have revealed inconsistent results in patients harboring mutations in…”
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Right-to-Left Shunt in CADASIL Patients : Prevalence and Correlation With Clinical and MRI Findings by ZICARI, Enza, TASSI, Rossana, STROMILLO, Maria L, PELLEGRINI, Michele, BIANCHI, Silvia, CEVENINI, Gabriele, GISTRI, Massimo, DE STEFANO, Nicola, FEDERICO, Antonio, DOTTI, Maria T

“…A high prevalence of right-to-left shunt (RLS) was described in a family of patients with CADASIL, a rare cerebral arteriopathy attributable to Notch3 gene…”
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Cardiac autonomic nervous system and risk of arrhythmias in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) by RUFA, Alessandra, GUIDERI, Francesca, ACAMPA, Maurizio, CEVENINI, Gabriele, BIANCHI, Silvia, DE STEFANO, Nicola, STROMILLO, Maria L, FEDERICO, Antonio, DOTTI, Maria T

“…Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is an inherited systemic microangiopathy with prevalently…”
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Magnetic resonance imaging and spectroscopic changes in brains of patients with cerebrotendinous xanthomatosis by De Stefano, Nicola, Dotti, Maria T., Mortilla, Marzia, Federico, A.

“…Cerebrotendinous xanthomatosis (CTX) is a rare disorder due to an inherited defect in the metabolic pathway of cholesterol. Early diagnosis of the disease is…”
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Cortical damage in brains of patients with adult-form of myotonic dystrophy type 1 and no or minimal MRI abnormalities by GIORGIO, Antonio, DOTTI, Maria T, BATTAGLINI, Marco, MARINO, Silvia, MORTILLA, Marzia, STROMILLO, Maria L, BRAMANTI, Placido, ORRICO, Alfredo, FEDERICO, Antonio, DE STEFANO, Nicola

“…To evaluate, by using quantitative MRI metrics, subtle cortical changes in brains of patients with the adult form of myotonic dystrophy type I (DM1) who showed…”
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Severe metabolic abnormalities in the white matter of patients with vacuolating megalencephalic leukoencephalopathy with subcortical cysts. A proton MR spectroscopic imaging study by DE STEFANO, Nicola, BALESTRI, Paolo, DOTTI, Maria T, GROSSO, Salvatore, MORTILLA, Marzia, MORGESE, Guido, FEDERICO, Antonio

“…Vacuolating megalencephalic leukoencephalopathy (VML) with subcortical cysts is a neurodegenerative disorder clinically characterized by megalencephaly with…”
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Quantification of Brain Damage in Cerebrotendinous Xanthomatosis with Magnetization Transfer MR Imaging by Inglese, Matilde, DeStefano, Nicola, Pagani, Elisabetta, Dotti, Maria T, Comi, Giancarlo, Federico, Antonio, Filippi, Massimo

“…Conventional MR imaging for quantification of brain damage in monitoring the evolution of cerebrotendinous xanthomatosis (CTX) has limitations. Magnetization…”
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MR evidence of structural and metabolic changes in brains of patients with Werner's syndrome by DE STEFANO, Nicola, DOTTI, Maria T, BATTISTI, Carla, SICURELLI, Francesco, STROMILLO, Maria L, MORTILLA, Marzia, FEDERICO, Antonio

“…To assess CNS abnormalities in patients with Werner's syndrome (WS) using MR metrics specific for tissue damage. WS is a rare autosomal recessive disorder that…”
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Allogeneic haematopoietic stem cell transplantation for mitochondrial neurogastrointestinal encephalomyopathy by Halter, Joerg P, Michael, W, Schüpbach, M, Mandel, Hanna, Casali, Carlo, Orchard, Kim, Collin, Matthew, Valcarcel, David, Rovelli, Attilio, Filosto, Massimiliano, Dotti, Maria T, Marotta, Giuseppe, Pintos, Guillem, Barba, Pere, Accarino, Anna, Ferra, Christelle, Illa, Isabel, Beguin, Yves, Bakker, Jaap A, Boelens, Jaap J, de Coo, Irenaeus F M, Fay, Keith, Sue, Carolyn M, Nachbaur, David, Zoller, Heinz, Sobreira, Claudia, Pinto Simoes, Belinda, Hammans, Simon R, Savage, David, Martí, Ramon, Chinnery, Patrick F, Elhasid, Ronit, Gratwohl, Alois, Hirano, Michio

“…Haematopoietic stem cell transplantation has been proposed as treatment for mitochondrial neurogastrointestinal encephalomyopathy, a rare fatal autosomal…”
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APOE ɛ 2 is associated with white matter hyperintensity volume in CADASIL by Gesierich, Benno, Opherk, Christian, Rosand, Jonathan, Gonik, Mariya, Malik, Rainer, Jouvent, Eric, Hervé, Dominique, Adib-Samii, Poneh, Bevan, Steve, Pianese, Luigi, Silvestri, Serena, Dotti, Maria T, De Stefano, Nicola, van der Grond, Jeroen, Boon, Elles M J, Pescini, Francesca, Rost, Natalia, Pantoni, Leonardo, Lesnik Oberstein, Saskia A, Federico, Antonio, Ragno, Michele, Markus, Hugh S, Tournier-Lasserve, Elisabeth, Chabriat, Hugues, Dichgans, Martin, Duering, Marco, Ewers, Michael

“…Apolipoprotein E ( APOE) increases the risk for Alzheimer’s disease ( ɛ4 allele) and cerebral amyloid angiopathy ( ɛ2 and ɛ4), but its role in small vessel…”
Get full text