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Anna De Rosa

Showing results (71-80 of 116) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|May 4, 2011
The LRRK2 R1441C mutation is more frequent than G2019S in Parkinson's disease patients from southern ItalyChiara Criscuolo, Anna De Rosa, Anna Guacci, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 21, 2012
Non-motor symptoms in early Parkinson's disease: a 2-year follow-up study on previously untreated patientsRoberto Erro, Marina Picillo, Carmine Vitale, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 22, 2019
The flavor test is a sensitive tool in identifying the flavor sensorineural dysfunction in Parkinson's diseaseAnna De Rosa, Immacolata Cristina Nettore, Elena Cantone, et al.
Neurology|May 20, 2014
Postganglionic sudomotor denervation in patients with multiple system atrophyVincenzo Provitera, Maria Nolano, Giuseppe Caporaso, et al.
Journal of Neurology|February 8, 2012
Link between non-motor symptoms and cognitive dysfunctions in de novo, drug-naive PD patientsRoberto Erro, Gabriella Santangelo, Marina Picillo, et al.
Parkinsonism & Related Disorders|April 15, 2014
Is serum uric acid related to non-motor symptoms in de-novo Parkinson's disease patients?Marcello Moccia, Marina Picillo, Roberto Erro, et al.
Journal of Neurology|May 28, 2022
Screening for RFC-1 pathological expansion in late-onset ataxias: a contribution to the differential diagnosisMelissa Barghigiani, Giovanna De Michele, Alessandra Tessa, et al.
Journal of Neurology|August 31, 2013
Gender differences in non-motor symptoms in early, drug naïve Parkinson's diseaseMarina Picillo, Marianna Amboni, Roberto Erro, et al.
BMC Neurology|November 8, 2020
A case report of late-onset cerebellar ataxia associated with a rare p.R342W TGM6 (SCA35) mutationArianna Manini, Tommaso Bocci, Alice Migazzi, et al.
Journal of Nuclear Cardiology : Official Publication of the American Society of Nuclear Cardiology|August 18, 2020
Autonomic disorders and myocardial 123I-metaiodobenzylguanidine scintigraphy in Huntington's diseaseRoberta Assante, Elena Salvatore, Carmela Nappi, et al.
Pageof 12

Showing results (71-80 of 116) with videos related to

Sort By:
Pageof 12
Movement Disorders : Official Journal of the Movement Disorder Society|May 4, 2011
The LRRK2 R1441C mutation is more frequent than G2019S in Parkinson's disease patients from southern ItalyChiara Criscuolo, Anna De Rosa, Anna Guacci, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 21, 2012
Non-motor symptoms in early Parkinson's disease: a 2-year follow-up study on previously untreated patientsRoberto Erro, Marina Picillo, Carmine Vitale, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 22, 2019
The flavor test is a sensitive tool in identifying the flavor sensorineural dysfunction in Parkinson's diseaseAnna De Rosa, Immacolata Cristina Nettore, Elena Cantone, et al.
Neurology|May 20, 2014
Postganglionic sudomotor denervation in patients with multiple system atrophyVincenzo Provitera, Maria Nolano, Giuseppe Caporaso, et al.
Journal of Neurology|February 8, 2012
Link between non-motor symptoms and cognitive dysfunctions in de novo, drug-naive PD patientsRoberto Erro, Gabriella Santangelo, Marina Picillo, et al.
Parkinsonism & Related Disorders|April 15, 2014
Is serum uric acid related to non-motor symptoms in de-novo Parkinson's disease patients?Marcello Moccia, Marina Picillo, Roberto Erro, et al.
Journal of Neurology|May 28, 2022
Screening for RFC-1 pathological expansion in late-onset ataxias: a contribution to the differential diagnosisMelissa Barghigiani, Giovanna De Michele, Alessandra Tessa, et al.
Journal of Neurology|August 31, 2013
Gender differences in non-motor symptoms in early, drug naïve Parkinson's diseaseMarina Picillo, Marianna Amboni, Roberto Erro, et al.
BMC Neurology|November 8, 2020
A case report of late-onset cerebellar ataxia associated with a rare p.R342W TGM6 (SCA35) mutationArianna Manini, Tommaso Bocci, Alice Migazzi, et al.
Journal of Nuclear Cardiology : Official Publication of the American Society of Nuclear Cardiology|August 18, 2020
Autonomic disorders and myocardial 123I-metaiodobenzylguanidine scintigraphy in Huntington's diseaseRoberta Assante, Elena Salvatore, Carmela Nappi, et al.
Pageof 12