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Andreina Bordoni

Showing results (21-30 of 54) with videos related to

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Scientific Reports|April 7, 2017
Genome-wide RNA-seq of iPSC-derived motor neurons indicates selective cytoskeletal perturbation in Brown-Vialetto disease that is partially rescued by riboflavinFederica Rizzo, Agnese Ramirez, Claudia Compagnucci, et al.
Human Molecular Genetics|August 11, 2016
Selective mitochondrial depletion, apoptosis resistance, and increased mitophagy in human Charcot-Marie-Tooth 2A motor neuronsFederica Rizzo, Dario Ronchi, Sabrina Salani, et al.
Journal of Neurology|June 26, 2008
Novel Twinkle (PEO1) gene mutations in mendelian progressive external ophthalmoplegiaRoberta Virgilio, Dario Ronchi, Georgios M Hadjigeorgiou, et al.
Frontiers in Genetics|August 28, 2020
<i>TYMP</i> Variants Result in Late-Onset Mitochondrial Myopathy With Altered Muscle Mitochondrial DNA HomeostasisDario Ronchi, Leonardo Caporali, Giulia Francesca Manenti, et al.
Human Molecular Genetics|December 13, 2005
Transplanted ALDHhiSSClo neural stem cells generate motor neurons and delay disease progression of nmd mice, an animal model of SMARD1Stefania Corti, Federica Locatelli, Dimitra Papadimitriou, et al.
Journal of the Neurological Sciences|September 20, 2005
A case of CPT deficiency, homoplasmic mtDNA mutation and ragged red fibers at muscle biopsyMonica Sciacco, Alessandro Prelle, Gigliola Fagiolari, 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.
Journal of Medical Genetics|December 18, 2012
Riboflavin transporter 3 involvement in infantile Brown-Vialetto-Van Laere disease: two novel mutationsMarianna Ciccolella, Stefania Corti, Michela Catteruccia, et al.
Journal of Neuroscience Research|August 17, 2018
Purkinje cell COX deficiency and mtDNA depletion in an animal model of spinocerebellar ataxia type 1Michela Ripolone, Valeria Lucchini, Dario Ronchi, et al.
Journal of the Neurological Sciences|November 13, 2008
Amyotrophic lateral sclerosis linked to a novel SOD1 mutation with muscle mitochondrial dysfunctionStefania Corti, Chiara Donadoni, Dario Ronchi, et al.
Pageof 6

Showing results (21-30 of 54) with videos related to

Sort By:
Pageof 6
Scientific Reports|April 7, 2017
Genome-wide RNA-seq of iPSC-derived motor neurons indicates selective cytoskeletal perturbation in Brown-Vialetto disease that is partially rescued by riboflavinFederica Rizzo, Agnese Ramirez, Claudia Compagnucci, et al.
Human Molecular Genetics|August 11, 2016
Selective mitochondrial depletion, apoptosis resistance, and increased mitophagy in human Charcot-Marie-Tooth 2A motor neuronsFederica Rizzo, Dario Ronchi, Sabrina Salani, et al.
Journal of Neurology|June 26, 2008
Novel Twinkle (PEO1) gene mutations in mendelian progressive external ophthalmoplegiaRoberta Virgilio, Dario Ronchi, Georgios M Hadjigeorgiou, et al.
Frontiers in Genetics|August 28, 2020
<i>TYMP</i> Variants Result in Late-Onset Mitochondrial Myopathy With Altered Muscle Mitochondrial DNA HomeostasisDario Ronchi, Leonardo Caporali, Giulia Francesca Manenti, et al.
Human Molecular Genetics|December 13, 2005
Transplanted ALDHhiSSClo neural stem cells generate motor neurons and delay disease progression of nmd mice, an animal model of SMARD1Stefania Corti, Federica Locatelli, Dimitra Papadimitriou, et al.
Journal of the Neurological Sciences|September 20, 2005
A case of CPT deficiency, homoplasmic mtDNA mutation and ragged red fibers at muscle biopsyMonica Sciacco, Alessandro Prelle, Gigliola Fagiolari, 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.
Journal of Medical Genetics|December 18, 2012
Riboflavin transporter 3 involvement in infantile Brown-Vialetto-Van Laere disease: two novel mutationsMarianna Ciccolella, Stefania Corti, Michela Catteruccia, et al.
Journal of Neuroscience Research|August 17, 2018
Purkinje cell COX deficiency and mtDNA depletion in an animal model of spinocerebellar ataxia type 1Michela Ripolone, Valeria Lucchini, Dario Ronchi, et al.
Journal of the Neurological Sciences|November 13, 2008
Amyotrophic lateral sclerosis linked to a novel SOD1 mutation with muscle mitochondrial dysfunctionStefania Corti, Chiara Donadoni, Dario Ronchi, et al.
Pageof 6