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Francesca Magri

Showing results (91-100 of 174) with videos related to

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BMC Neurology|April 24, 2023
Ischemic optic neuropathy as first presentation in patient with m.3243 A > G MELAS classic mutationSimone Scarcella, Laura Dell'Arti, Delia Gagliardi, et al.
International Journal of Molecular Sciences|September 9, 2022
Antisense Morpholino-Based In Vitro Correction of a Pseudoexon-Generating Variant in the <i>SGCB</i> GeneFrancesca Magri, Simona Zanotti, Sabrina Salani, et al.
Frontiers in Neurology|August 18, 2018
Bilateral Cavernous Carotid Aneurysms: Atypical Presentation of a Rare Cause of Mass Effect. A Case Report and a Review of the LiteratureDelia Gagliardi, Irene Faravelli, Luisa Villa, et al.
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.
Frontiers in Neurology|October 31, 2018
Stormorken Syndrome Caused by a p.R304W <i>STIM1</i> Mutation: The First Italian Patient and a Review of the LiteratureOscar Borsani, Daniela Piga, Stefania Costa, et al.
BMC Neurology|March 19, 2026
A new MYH2 variant in an Italian patient expanding the clinical spectrum of MYH2-related myopathySimona Zanotti, Dario Ronchi, Laura Napoli, 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.
Experimental Cell Research|March 20, 2012
Direct reprogramming of human astrocytes into neural stem cells and neuronsStefania Corti, Monica Nizzardo, Chiara Simone, 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.
Acta Neuropathologica Communications|April 9, 2022
Muscle histological changes in a large cohort of patients affected with Becker muscular dystrophyMichela Ripolone, Daniele Velardo, Stefania Mondello, et al.
Pageof 18

Showing results (91-100 of 174) with videos related to

Sort By:
Pageof 18
BMC Neurology|April 24, 2023
Ischemic optic neuropathy as first presentation in patient with m.3243 A > G MELAS classic mutationSimone Scarcella, Laura Dell'Arti, Delia Gagliardi, et al.
International Journal of Molecular Sciences|September 9, 2022
Antisense Morpholino-Based In Vitro Correction of a Pseudoexon-Generating Variant in the <i>SGCB</i> GeneFrancesca Magri, Simona Zanotti, Sabrina Salani, et al.
Frontiers in Neurology|August 18, 2018
Bilateral Cavernous Carotid Aneurysms: Atypical Presentation of a Rare Cause of Mass Effect. A Case Report and a Review of the LiteratureDelia Gagliardi, Irene Faravelli, Luisa Villa, et al.
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.
Frontiers in Neurology|October 31, 2018
Stormorken Syndrome Caused by a p.R304W <i>STIM1</i> Mutation: The First Italian Patient and a Review of the LiteratureOscar Borsani, Daniela Piga, Stefania Costa, et al.
BMC Neurology|March 19, 2026
A new MYH2 variant in an Italian patient expanding the clinical spectrum of MYH2-related myopathySimona Zanotti, Dario Ronchi, Laura Napoli, 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.
Experimental Cell Research|March 20, 2012
Direct reprogramming of human astrocytes into neural stem cells and neuronsStefania Corti, Monica Nizzardo, Chiara Simone, 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.
Acta Neuropathologica Communications|April 9, 2022
Muscle histological changes in a large cohort of patients affected with Becker muscular dystrophyMichela Ripolone, Daniele Velardo, Stefania Mondello, et al.
Pageof 18