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Giuseppe Nicoletti

Showing results (81-90 of 112) with videos related to

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Journal of Neuroscience Research|June 5, 2007
Carnosine interaction with nitric oxide and astroglial cell protectionVincenzo Giuseppe Nicoletti, Anna Maria Santoro, Giulia Grasso, et al.
Parkinsonism & Related Disorders|August 30, 2008
Compound heterozygosity in DJ-1 gene non-coding portion related to parkinsonismPatrizia Tarantino, Donatella Civitelli, Ferdinanda Annesi, et al.
Clinical Neuropharmacology|May 1, 2002
Body weight influences pharmacokinetics of levodopa in Parkinson's diseaseMario Zappia, Lucia Crescibene, Gennarina Arabia, et al.
Annals of Neurology|July 12, 2002
Further evidence that SPG3A gene mutations cause autosomal dominant hereditary spastic paraplegiaMaria Muglia, Angela Magariello, Giuseppe Nicoletti, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 7, 2010
An magnetic resonance imaging T2*-weighted sequence at short echo time to detect putaminal hypointensity in ParkinsonismsGennarina Arabia, Maurizio Morelli, Sandra Paglionico, et al.
Parkinsonism & Related Disorders|April 7, 2016
Cerebellar involvement in essential tremor with and without resting tremor: A Diffusion Tensor Imaging studyFabiana Novellino, Giuseppe Nicoletti, Andrea Cherubini, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 25, 2010
Lack of association between G-protein coupled receptor kinase 5 gene and Parkinson's diseasePatrizia Tarantino, Elvira Valeria De Marco, Grazia Annesi, et al.
Archives of Neurology|March 17, 2004
Increased risk for Alzheimer disease with the interaction of MPO and A2M polymorphismsMario Zappia, Ida Manna, Paolo Serra, et al.
Cells|April 4, 2019
The Copper(II)-Assisted Connection between NGF and BDNF by Means of Nerve Growth Factor-Mimicking Short PeptidesIrina Naletova, Cristina Satriano, Adriana Pietropaolo, et al.
Journal of Neurology|October 17, 2002
A large family with pure autosomal dominant hereditary spastic paraplegia from southern Italy mapping to chromosome 14q11.2-q24.3Maria Muglia, Angela Magariello, Giuseppe Nicoletti, et al.
Pageof 12

Showing results (81-90 of 112) with videos related to

Sort By:
Pageof 12
Journal of Neuroscience Research|June 5, 2007
Carnosine interaction with nitric oxide and astroglial cell protectionVincenzo Giuseppe Nicoletti, Anna Maria Santoro, Giulia Grasso, et al.
Parkinsonism & Related Disorders|August 30, 2008
Compound heterozygosity in DJ-1 gene non-coding portion related to parkinsonismPatrizia Tarantino, Donatella Civitelli, Ferdinanda Annesi, et al.
Clinical Neuropharmacology|May 1, 2002
Body weight influences pharmacokinetics of levodopa in Parkinson's diseaseMario Zappia, Lucia Crescibene, Gennarina Arabia, et al.
Annals of Neurology|July 12, 2002
Further evidence that SPG3A gene mutations cause autosomal dominant hereditary spastic paraplegiaMaria Muglia, Angela Magariello, Giuseppe Nicoletti, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 7, 2010
An magnetic resonance imaging T2*-weighted sequence at short echo time to detect putaminal hypointensity in ParkinsonismsGennarina Arabia, Maurizio Morelli, Sandra Paglionico, et al.
Parkinsonism & Related Disorders|April 7, 2016
Cerebellar involvement in essential tremor with and without resting tremor: A Diffusion Tensor Imaging studyFabiana Novellino, Giuseppe Nicoletti, Andrea Cherubini, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 25, 2010
Lack of association between G-protein coupled receptor kinase 5 gene and Parkinson's diseasePatrizia Tarantino, Elvira Valeria De Marco, Grazia Annesi, et al.
Archives of Neurology|March 17, 2004
Increased risk for Alzheimer disease with the interaction of MPO and A2M polymorphismsMario Zappia, Ida Manna, Paolo Serra, et al.
Cells|April 4, 2019
The Copper(II)-Assisted Connection between NGF and BDNF by Means of Nerve Growth Factor-Mimicking Short PeptidesIrina Naletova, Cristina Satriano, Adriana Pietropaolo, et al.
Journal of Neurology|October 17, 2002
A large family with pure autosomal dominant hereditary spastic paraplegia from southern Italy mapping to chromosome 14q11.2-q24.3Maria Muglia, Angela Magariello, Giuseppe Nicoletti, et al.
Pageof 12