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Nereo Bresolin

Showing results (151-160 of 346) with videos related to

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Neurobiology of Aging|January 10, 2006
Oxidative imbalance in patients with mild cognitive impairment and Alzheimer's diseaseIlaria Guidi, Daniela Galimberti, Silvia Lonati, et al.
Journal of Child Neurology|November 6, 2004
Study of attentional processes in children with idiopathic epilepsy by Conners' Continuous Performance TestRenato Borgatti, Paolo Piccinelli, Rosario Montirosso, et al.
Brain : a Journal of Neurology|January 11, 2015
CHCHD10 mutations in Italian patients with sporadic amyotrophic lateral sclerosisDario Ronchi, Giulietta Riboldi, Roberto Del Bo, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|November 22, 2021
Cell-penetrating peptide-conjugated Morpholino rescues SMA in a symptomatic preclinical modelMargherita Bersani, Mafalda Rizzuti, Elisa Pagliari, et al.
Cognitive and Behavioral Neurology : Official Journal of the Society for Behavioral and Cognitive Neurology|March 20, 2010
A cortically blind patient with preserved visual imageryStefano Zago, Stefania Corti, Anna Bersano, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 5, 2010
A wide spectrum of clinical, neurophysiological and neuroradiological abnormalities in a family with a novel CACNA1A mutationRomina Romaniello, Claudio Zucca, Alessandra Tonelli, et al.
Human Molecular Genetics|July 24, 2010
Systemic transplantation of c-kit+ cells exerts a therapeutic effect in a model of amyotrophic lateral sclerosisStefania Corti, Monica Nizzardo, Martina Nardini, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|August 5, 2018
Glucose-free/high-protein diet improves hepatomegaly and exercise intolerance in glycogen storage disease type III miceSerena Pagliarani, Sabrina Lucchiari, Gianna Ulzi, et al.
Journal of the Neurological Sciences|February 19, 2010
The m.12316G>A mutation in the mitochondrial tRNA Leu(CUN) gene is associated with mitochondrial myopathy and respiratory impairmentDario Ronchi, Roberta Virgilio, Andreina Bordoni, et al.
Scientific Reports|July 6, 2018
MicroRNA expression analysis identifies a subset of downregulated miRNAs in ALS motor neuron progenitorsMafalda Rizzuti, Giuseppe Filosa, Valentina Melzi, et al.
Pageof 35

Showing results (151-160 of 346) with videos related to

Sort By:
Pageof 35
Neurobiology of Aging|January 10, 2006
Oxidative imbalance in patients with mild cognitive impairment and Alzheimer's diseaseIlaria Guidi, Daniela Galimberti, Silvia Lonati, et al.
Journal of Child Neurology|November 6, 2004
Study of attentional processes in children with idiopathic epilepsy by Conners' Continuous Performance TestRenato Borgatti, Paolo Piccinelli, Rosario Montirosso, et al.
Brain : a Journal of Neurology|January 11, 2015
CHCHD10 mutations in Italian patients with sporadic amyotrophic lateral sclerosisDario Ronchi, Giulietta Riboldi, Roberto Del Bo, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|November 22, 2021
Cell-penetrating peptide-conjugated Morpholino rescues SMA in a symptomatic preclinical modelMargherita Bersani, Mafalda Rizzuti, Elisa Pagliari, et al.
Cognitive and Behavioral Neurology : Official Journal of the Society for Behavioral and Cognitive Neurology|March 20, 2010
A cortically blind patient with preserved visual imageryStefano Zago, Stefania Corti, Anna Bersano, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 5, 2010
A wide spectrum of clinical, neurophysiological and neuroradiological abnormalities in a family with a novel CACNA1A mutationRomina Romaniello, Claudio Zucca, Alessandra Tonelli, et al.
Human Molecular Genetics|July 24, 2010
Systemic transplantation of c-kit+ cells exerts a therapeutic effect in a model of amyotrophic lateral sclerosisStefania Corti, Monica Nizzardo, Martina Nardini, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|August 5, 2018
Glucose-free/high-protein diet improves hepatomegaly and exercise intolerance in glycogen storage disease type III miceSerena Pagliarani, Sabrina Lucchiari, Gianna Ulzi, et al.
Journal of the Neurological Sciences|February 19, 2010
The m.12316G>A mutation in the mitochondrial tRNA Leu(CUN) gene is associated with mitochondrial myopathy and respiratory impairmentDario Ronchi, Roberta Virgilio, Andreina Bordoni, et al.
Scientific Reports|July 6, 2018
MicroRNA expression analysis identifies a subset of downregulated miRNAs in ALS motor neuron progenitorsMafalda Rizzuti, Giuseppe Filosa, Valentina Melzi, et al.
Pageof 35