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Selina Piazza

Showing results (1-10 of 11) with videos related to

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Bioscience Reports|May 12, 2007
Functional diagnostics in mitochondrial diseasesGabriele Siciliano, Leda Volpi, Selina Piazza, et al.
Journal of Computer Assisted Tomography|September 24, 2010
Evaluation of corticospinal tract impairment in the brain of patients with amyotrophic lateral sclerosis by using diffusion tensor imaging acquisition schemes with different numbers of diffusion-weighting directionsMirco Cosottini, Marco Giannelli, Francesca Vannozzi, et al.
Plos One|July 23, 2013
Mapping cortical degeneration in ALS with magnetization transfer ratio and voxel-based morphometryMirco Cosottini, Paolo Cecchi, Selina Piazza, et al.
Archives Italiennes De Biologie|March 18, 2011
Strategies for clinical approach to neurodegeneration in Amyotrophic lateral sclerosisCecilia Carlesi, Livia Pasquali, Selina Piazza, et al.
Experimental Neurology|January 10, 2012
Structural and functional evaluation of cortical motor areas in Amyotrophic Lateral SclerosisMirco Cosottini, Ilaria Pesaresi, Selina Piazza, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|February 27, 2010
D90A-SOD1 mutation in ALS: The first report of heterozygous Italian patients and unusual findingsFabio Giannini, Stefania Battistini, Michelangelo Mancuso, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 10, 2008
The first Italian family with evidence of pyramidal impairment as phenotypic manifestation of Silver syndrome BSCL2 gene mutationGianfranco Cafforio, Rosanna Calabrese, Nicola Morelli, et al.
Neurobiology of Aging|May 17, 2008
Lack of association between the APEX1 Asp148Glu polymorphism and sporadic amyotrophic lateral sclerosisFabio Coppedè, Annalisa Lo Gerfo, Cecilia Carlesi, et al.
Neuromuscular Disorders : NMD|September 21, 2010
A new truncating MPZ mutation associated with a very mild CMT1 B phenotypeSelina Piazza, Fulvia Baldinotti, Antonella Fogli, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 14, 2011
Nerve and muscle involvement in mitochondrial disorders: an electrophysiological studyMichelangelo Mancuso, Selina Piazza, Leda Volpi, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Bioscience Reports|May 12, 2007
Functional diagnostics in mitochondrial diseasesGabriele Siciliano, Leda Volpi, Selina Piazza, et al.
Journal of Computer Assisted Tomography|September 24, 2010
Evaluation of corticospinal tract impairment in the brain of patients with amyotrophic lateral sclerosis by using diffusion tensor imaging acquisition schemes with different numbers of diffusion-weighting directionsMirco Cosottini, Marco Giannelli, Francesca Vannozzi, et al.
Plos One|July 23, 2013
Mapping cortical degeneration in ALS with magnetization transfer ratio and voxel-based morphometryMirco Cosottini, Paolo Cecchi, Selina Piazza, et al.
Archives Italiennes De Biologie|March 18, 2011
Strategies for clinical approach to neurodegeneration in Amyotrophic lateral sclerosisCecilia Carlesi, Livia Pasquali, Selina Piazza, et al.
Experimental Neurology|January 10, 2012
Structural and functional evaluation of cortical motor areas in Amyotrophic Lateral SclerosisMirco Cosottini, Ilaria Pesaresi, Selina Piazza, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|February 27, 2010
D90A-SOD1 mutation in ALS: The first report of heterozygous Italian patients and unusual findingsFabio Giannini, Stefania Battistini, Michelangelo Mancuso, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 10, 2008
The first Italian family with evidence of pyramidal impairment as phenotypic manifestation of Silver syndrome BSCL2 gene mutationGianfranco Cafforio, Rosanna Calabrese, Nicola Morelli, et al.
Neurobiology of Aging|May 17, 2008
Lack of association between the APEX1 Asp148Glu polymorphism and sporadic amyotrophic lateral sclerosisFabio Coppedè, Annalisa Lo Gerfo, Cecilia Carlesi, et al.
Neuromuscular Disorders : NMD|September 21, 2010
A new truncating MPZ mutation associated with a very mild CMT1 B phenotypeSelina Piazza, Fulvia Baldinotti, Antonella Fogli, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 14, 2011
Nerve and muscle involvement in mitochondrial disorders: an electrophysiological studyMichelangelo Mancuso, Selina Piazza, Leda Volpi, et al.
Pageof 2