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Stefania Corti

Showing results (181-190 of 287) with videos related to

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Brain : a Journal of Neurology|April 25, 2024
Unleashing the potential of mRNA therapeutics for inherited neurological diseasesEdoardo Monfrini, Giacomo Baso, Dario Ronchi, 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.
Experimental Cell Research|March 31, 2004
Skeletal muscle differentiation potential of human adult bone marrow cellsPatrizia Bossolasco, Stefania Corti, Sandra Strazzer, 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.
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.
The FEBS Journal|January 24, 2026
Regulation of PHOX2B gene expression by the long non-coding natural antisense RNA PHOX2B-AS1Simona Di Lascio, Ana Lucia Cuadros Gamboa, Martina Bertocchi, 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.
Experimental Cell Research|March 20, 2012
Direct reprogramming of human astrocytes into neural stem cells and neuronsStefania Corti, Monica Nizzardo, Chiara Simone, 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.
Pageof 29

Showing results (181-190 of 287) with videos related to

Sort By:
Pageof 29
Brain : a Journal of Neurology|April 25, 2024
Unleashing the potential of mRNA therapeutics for inherited neurological diseasesEdoardo Monfrini, Giacomo Baso, Dario Ronchi, 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.
Experimental Cell Research|March 31, 2004
Skeletal muscle differentiation potential of human adult bone marrow cellsPatrizia Bossolasco, Stefania Corti, Sandra Strazzer, 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.
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.
The FEBS Journal|January 24, 2026
Regulation of PHOX2B gene expression by the long non-coding natural antisense RNA PHOX2B-AS1Simona Di Lascio, Ana Lucia Cuadros Gamboa, Martina Bertocchi, 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.
Experimental Cell Research|March 20, 2012
Direct reprogramming of human astrocytes into neural stem cells and neuronsStefania Corti, Monica Nizzardo, Chiara Simone, 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.
Pageof 29