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Nereo Bresolin

Showing results (231-240 of 346) with videos related to

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Journal of the Neurological Sciences|December 27, 2011
Optic atrophy plus phenotype due to mutations in the OPA1 gene: two more Italian familiesMichela Ranieri, Roberto Del Bo, Andreina Bordoni, et al.
BMC Neurology|September 26, 2015
ISPD mutations account for a small proportion of Italian Limb Girdle Muscular Dystrophy casesFrancesca Magri, Irene Colombo, Roberto Del Bo, et al.
Journal of Alzheimer'S Disease : JAD|May 11, 2012
Early onset behavioral variant frontotemporal dementia due to the C9ORF72 hexanucleotide repeat expansion: psychiatric clinical presentationsAndrea Arighi, Giorgio G Fumagalli, Francesca Jacini, et al.
Brain : a Journal of Neurology|December 25, 2009
Embryonic stem cell-derived neural stem cells improve spinal muscular atrophy phenotype in miceStefania Corti, Monica Nizzardo, Martina Nardini, et al.
Neuroscience Letters|August 31, 2011
Expression and genetic analysis of miRNAs involved in CD4+ cell activation in patients with multiple sclerosisChiara Fenoglio, Claudia Cantoni, Milena De Riz, et al.
Experimental Neurology|February 8, 2011
Beta-lactam antibiotic offers neuroprotection in a spinal muscular atrophy model by multiple mechanismsMonica Nizzardo, Martina Nardini, Dario Ronchi, et al.
Annals of Neurosciences|September 11, 2014
Beta-lactam antibiotic offers neuroprotection in a spinal muscular atrophy model by multiple mechanisms: Experimental Neurology 2011; 229: 214-225Monica Nizzardo, Martina Nardini, Dario Ronchi, et al.
Science (New York, N.Y.)|July 12, 2003
Cell therapy of alpha-sarcoglycan null dystrophic mice through intra-arterial delivery of mesoangioblastsMaurilio Sampaolesi, Yvan Torrente, Anna Innocenzi, et al.
Annals of Clinical and Translational Neurology|May 4, 2021
Charcot-Marie-Tooth disease type 2F associated with biallelic HSPB1 mutationsElena Abati, Stefania Magri, Megi Meneri, et al.
Neurobiology of Aging|August 16, 2005
Is M129V of PRNP gene associated with Alzheimer's disease? A case-control study and a meta-analysisRoberto Del Bo, Marina Scarlato, Serena Ghezzi, et al.
Pageof 35

Showing results (231-240 of 346) with videos related to

Sort By:
Pageof 35
Journal of the Neurological Sciences|December 27, 2011
Optic atrophy plus phenotype due to mutations in the OPA1 gene: two more Italian familiesMichela Ranieri, Roberto Del Bo, Andreina Bordoni, et al.
BMC Neurology|September 26, 2015
ISPD mutations account for a small proportion of Italian Limb Girdle Muscular Dystrophy casesFrancesca Magri, Irene Colombo, Roberto Del Bo, et al.
Journal of Alzheimer'S Disease : JAD|May 11, 2012
Early onset behavioral variant frontotemporal dementia due to the C9ORF72 hexanucleotide repeat expansion: psychiatric clinical presentationsAndrea Arighi, Giorgio G Fumagalli, Francesca Jacini, et al.
Brain : a Journal of Neurology|December 25, 2009
Embryonic stem cell-derived neural stem cells improve spinal muscular atrophy phenotype in miceStefania Corti, Monica Nizzardo, Martina Nardini, et al.
Neuroscience Letters|August 31, 2011
Expression and genetic analysis of miRNAs involved in CD4+ cell activation in patients with multiple sclerosisChiara Fenoglio, Claudia Cantoni, Milena De Riz, et al.
Experimental Neurology|February 8, 2011
Beta-lactam antibiotic offers neuroprotection in a spinal muscular atrophy model by multiple mechanismsMonica Nizzardo, Martina Nardini, Dario Ronchi, et al.
Annals of Neurosciences|September 11, 2014
Beta-lactam antibiotic offers neuroprotection in a spinal muscular atrophy model by multiple mechanisms: Experimental Neurology 2011; 229: 214-225Monica Nizzardo, Martina Nardini, Dario Ronchi, et al.
Science (New York, N.Y.)|July 12, 2003
Cell therapy of alpha-sarcoglycan null dystrophic mice through intra-arterial delivery of mesoangioblastsMaurilio Sampaolesi, Yvan Torrente, Anna Innocenzi, et al.
Annals of Clinical and Translational Neurology|May 4, 2021
Charcot-Marie-Tooth disease type 2F associated with biallelic HSPB1 mutationsElena Abati, Stefania Magri, Megi Meneri, et al.
Neurobiology of Aging|August 16, 2005
Is M129V of PRNP gene associated with Alzheimer's disease? A case-control study and a meta-analysisRoberto Del Bo, Marina Scarlato, Serena Ghezzi, et al.
Pageof 35