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Nereo Bresolin

Showing results (241-250 of 346) with videos related to

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Neuroscience Letters|July 26, 2005
P-selectin glycoprotein ligand-1 variable number of tandem repeats (VNTR) polymorphism in patients with multiple sclerosisDiego Scalabrini, Daniela Galimberti, Chiara Fenoglio, et al.
Genome Biology and Evolution|April 1, 2014
Ancient and recent selective pressures shaped genetic diversity at AIM2-like nucleic acid sensorsRachele Cagliani, Diego Forni, Mara Biasin, et al.
Neurology. Genetics|October 16, 2020
Expanding the clinical spectrum of the mitochondrial mutation A13084T in the <i>ND5</i> geneRoberta Brusa, Eleonora Mauri, Laura Dell'Arti, et al.
Journal of the Neurological Sciences|October 31, 2007
Gender-specific influence of the chromosome 16 chemokine gene cluster on the susceptibility to Multiple SclerosisDaniela Galimberti, Diego Scalabrini, Chiara Fenoglio, et al.
Cell Transplantation|April 18, 2007
Induction of neurotrophin expression via human adult mesenchymal stem cells: implication for cell therapy in neurodegenerative diseasesFederica Pisati, Patrizia Bossolasco, Mirella Meregalli, et al.
Journal of the Neurological Sciences|October 7, 2004
CCR2-64I polymorphism and CCR5Delta32 deletion in patients with Alzheimer's diseaseDaniela Galimberti, Chiara Fenoglio, Carlo Lovati, et al.
Experimental Cell Research|March 20, 2012
Direct reprogramming of human astrocytes into neural stem cells and neuronsStefania Corti, Monica Nizzardo, Chiara Simone, et al.
Annals of Clinical and Translational Neurology|April 25, 2020
Dystonia-ataxia syndrome with permanent torsional nystagmus caused by ECHS1 deficiencyDario Ronchi, Edoardo Monfrini, Sara Bonato, et al.
Human Mutation|May 12, 2009
A novel CLN8 mutation in late-infantile-onset neuronal ceroid lipofuscinosis (LINCL) reveals aspects of CLN8 neurobiological functionChiara Vantaggiato, Francesca Redaelli, Sestina Falcone, et al.
Scientific Reports|April 14, 2022
Clinical and genetic features of a cohort of patients with MFN2-related neuropathyElena Abati, Arianna Manini, Daniele Velardo, et al.
Pageof 35

Showing results (241-250 of 346) with videos related to

Sort By:
Pageof 35
Neuroscience Letters|July 26, 2005
P-selectin glycoprotein ligand-1 variable number of tandem repeats (VNTR) polymorphism in patients with multiple sclerosisDiego Scalabrini, Daniela Galimberti, Chiara Fenoglio, et al.
Genome Biology and Evolution|April 1, 2014
Ancient and recent selective pressures shaped genetic diversity at AIM2-like nucleic acid sensorsRachele Cagliani, Diego Forni, Mara Biasin, et al.
Neurology. Genetics|October 16, 2020
Expanding the clinical spectrum of the mitochondrial mutation A13084T in the <i>ND5</i> geneRoberta Brusa, Eleonora Mauri, Laura Dell'Arti, et al.
Journal of the Neurological Sciences|October 31, 2007
Gender-specific influence of the chromosome 16 chemokine gene cluster on the susceptibility to Multiple SclerosisDaniela Galimberti, Diego Scalabrini, Chiara Fenoglio, et al.
Cell Transplantation|April 18, 2007
Induction of neurotrophin expression via human adult mesenchymal stem cells: implication for cell therapy in neurodegenerative diseasesFederica Pisati, Patrizia Bossolasco, Mirella Meregalli, et al.
Journal of the Neurological Sciences|October 7, 2004
CCR2-64I polymorphism and CCR5Delta32 deletion in patients with Alzheimer's diseaseDaniela Galimberti, Chiara Fenoglio, Carlo Lovati, et al.
Experimental Cell Research|March 20, 2012
Direct reprogramming of human astrocytes into neural stem cells and neuronsStefania Corti, Monica Nizzardo, Chiara Simone, et al.
Annals of Clinical and Translational Neurology|April 25, 2020
Dystonia-ataxia syndrome with permanent torsional nystagmus caused by ECHS1 deficiencyDario Ronchi, Edoardo Monfrini, Sara Bonato, et al.
Human Mutation|May 12, 2009
A novel CLN8 mutation in late-infantile-onset neuronal ceroid lipofuscinosis (LINCL) reveals aspects of CLN8 neurobiological functionChiara Vantaggiato, Francesca Redaelli, Sestina Falcone, et al.
Scientific Reports|April 14, 2022
Clinical and genetic features of a cohort of patients with MFN2-related neuropathyElena Abati, Arianna Manini, Daniele Velardo, et al.
Pageof 35