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Maria T Dotti

Showing results (1-10 of 17) with videos related to

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Acta Psychiatrica Scandinavica|August 13, 2005
Postpartum psychiatric disturbances as an unrecognized onset of CADASILLeonardo Pantoni, Francesca Pescini, Domenico Inzitari, et al.
Journal of Stroke and Cerebrovascular Diseases : the Official Journal of National Stroke Association|May 3, 2013
Visual system involvement in CADASILElena Pretegiani, Francesca Rosini, Maria T Dotti, et al.
Brain : a Journal of Neurology|March 1, 2011
Differences in saccade dynamics between spinocerebellar ataxia 2 and late-onset cerebellar ataxiasPamela Federighi, Gabriele Cevenini, Maria T Dotti, et al.
AJNR. American Journal of Neuroradiology|March 15, 2003
Quantification of brain damage in cerebrotendinous xanthomatosis with magnetization transfer MR imagingMatilde Inglese, Nicola De Stefano, Elisabetta Pagani, et al.
Journal of Neurology|October 31, 2003
MR evidence of structural and metabolic changes in brains of patients with Werner's syndromeNicola De Stefano, Maria T Dotti, Carla Battisti, et al.
Journal of the Peripheral Nervous System : JPNS|January 3, 2013
Sonographic and electrodiagnostic features of hereditary neuropathy with liability to pressure palsiesFederica Ginanneschi, Georgios Filippou, Fabio Giannini, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 21, 2014
Hand muscles corticomotor excitability in hereditary spastic paraparesis type 4Federica Ginanneschi, Maria A Carluccio, Andrea Mignarri, et al.
Journal of the Neurological Sciences|February 7, 2015
Eye movement changes in mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)Claudia Vinciguerra, Pamela Federighi, Francesca Rosini, et al.
Journal of Neurology|December 7, 2005
A novel mutation producing premature termination codon at the OPA1 gene causes autosomal dominant optic atrophyElena Cardaioli, Gian Nicola Gallus, Paola Da Pozzo, et al.
Stroke|January 16, 2007
Cardiac autonomic nervous system and risk of arrhythmias in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)Alessandra Rufa, Francesca Guideri, Maurizio Acampa, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Acta Psychiatrica Scandinavica|August 13, 2005
Postpartum psychiatric disturbances as an unrecognized onset of CADASILLeonardo Pantoni, Francesca Pescini, Domenico Inzitari, et al.
Journal of Stroke and Cerebrovascular Diseases : the Official Journal of National Stroke Association|May 3, 2013
Visual system involvement in CADASILElena Pretegiani, Francesca Rosini, Maria T Dotti, et al.
Brain : a Journal of Neurology|March 1, 2011
Differences in saccade dynamics between spinocerebellar ataxia 2 and late-onset cerebellar ataxiasPamela Federighi, Gabriele Cevenini, Maria T Dotti, et al.
AJNR. American Journal of Neuroradiology|March 15, 2003
Quantification of brain damage in cerebrotendinous xanthomatosis with magnetization transfer MR imagingMatilde Inglese, Nicola De Stefano, Elisabetta Pagani, et al.
Journal of Neurology|October 31, 2003
MR evidence of structural and metabolic changes in brains of patients with Werner's syndromeNicola De Stefano, Maria T Dotti, Carla Battisti, et al.
Journal of the Peripheral Nervous System : JPNS|January 3, 2013
Sonographic and electrodiagnostic features of hereditary neuropathy with liability to pressure palsiesFederica Ginanneschi, Georgios Filippou, Fabio Giannini, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 21, 2014
Hand muscles corticomotor excitability in hereditary spastic paraparesis type 4Federica Ginanneschi, Maria A Carluccio, Andrea Mignarri, et al.
Journal of the Neurological Sciences|February 7, 2015
Eye movement changes in mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)Claudia Vinciguerra, Pamela Federighi, Francesca Rosini, et al.
Journal of Neurology|December 7, 2005
A novel mutation producing premature termination codon at the OPA1 gene causes autosomal dominant optic atrophyElena Cardaioli, Gian Nicola Gallus, Paola Da Pozzo, et al.
Stroke|January 16, 2007
Cardiac autonomic nervous system and risk of arrhythmias in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)Alessandra Rufa, Francesca Guideri, Maurizio Acampa, et al.
Pageof 2