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Stefania Corti

Showing results (141-150 of 287) with videos related to

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European Journal of Histochemistry : EJH|September 1, 2022
Immunofluorescence signal intensity measurements as a semi-quantitative tool to assess sarcoglycan complex expression in muscle biopsySimona Zanotti, Francesca Magri, Francesca Poggetti, et al.
Frontiers in Cellular Neuroscience|March 26, 2025
Riboflavin transporter deficiency: <i>AAV9-SLC52A2</i> gene therapy as a new therapeutic strategyCecilia Mei, Valentina Magliocca, Xin Chen, et al.
Human Molecular Genetics|September 6, 2013
Minimally invasive transplantation of iPSC-derived ALDHhiSSCloVLA4+ neural stem cells effectively improves the phenotype of an amyotrophic lateral sclerosis modelMonica Nizzardo, Chiara Simone, Federica Rizzo, et al.
Journal of the Neurological Sciences|March 13, 2009
Mitochondrial DNA G8363A mutation in the tRNA Lys gene: clinical, biochemical and pathological studyRoberta Virgilio, Dario Ronchi, Andreina Bordoni, et al.
Medicine|October 30, 2020
Hyperacute extensive spinal cord infarction and negative spine magnetic resonance imaging: a case report and review of the literatureGianluca Costamagna, Megi Meneri, Elena Abati, et al.
Scientific Reports|July 1, 2015
Spinal muscular atrophy phenotype is ameliorated in human motor neurons by SMN increase via different novel RNA therapeutic approachesMonica Nizzardo, Chiara Simone, Sara Dametti, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|February 14, 2025
iPSC-derived human cortical organoids display profound alterations of cellular homeostasis following SARS-CoV-2 infection and Spike protein exposureGioia Cappelletti, Lorenzo Brambilla, Sergio Strizzi, et al.
Cellular and Molecular Life Sciences : CMLS|December 26, 2024
Targeting STMN2 for neuroprotection and neuromuscular recovery in Spinal Muscular Atrophy: evidence from in vitro and in vivo SMA modelsElisa Pagliari, Michela Taiana, Paolo Manzini, et al.
Frontiers in Neurology|August 29, 2019
Ophthalmoplegia Due to Miller Fisher Syndrome in a Patient With Myasthenia GravisRoberta Brusa, Irene Faravelli, Delia Gagliardi, et al.
Biochimica Et Biophysica Acta|August 6, 2014
Glycogen storage disease type III: A novel Agl knockout mouse modelSerena Pagliarani, Sabrina Lucchiari, Gianna Ulzi, et al.
Pageof 29

Showing results (141-150 of 287) with videos related to

Sort By:
Pageof 29
European Journal of Histochemistry : EJH|September 1, 2022
Immunofluorescence signal intensity measurements as a semi-quantitative tool to assess sarcoglycan complex expression in muscle biopsySimona Zanotti, Francesca Magri, Francesca Poggetti, et al.
Frontiers in Cellular Neuroscience|March 26, 2025
Riboflavin transporter deficiency: <i>AAV9-SLC52A2</i> gene therapy as a new therapeutic strategyCecilia Mei, Valentina Magliocca, Xin Chen, et al.
Human Molecular Genetics|September 6, 2013
Minimally invasive transplantation of iPSC-derived ALDHhiSSCloVLA4+ neural stem cells effectively improves the phenotype of an amyotrophic lateral sclerosis modelMonica Nizzardo, Chiara Simone, Federica Rizzo, et al.
Journal of the Neurological Sciences|March 13, 2009
Mitochondrial DNA G8363A mutation in the tRNA Lys gene: clinical, biochemical and pathological studyRoberta Virgilio, Dario Ronchi, Andreina Bordoni, et al.
Medicine|October 30, 2020
Hyperacute extensive spinal cord infarction and negative spine magnetic resonance imaging: a case report and review of the literatureGianluca Costamagna, Megi Meneri, Elena Abati, et al.
Scientific Reports|July 1, 2015
Spinal muscular atrophy phenotype is ameliorated in human motor neurons by SMN increase via different novel RNA therapeutic approachesMonica Nizzardo, Chiara Simone, Sara Dametti, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|February 14, 2025
iPSC-derived human cortical organoids display profound alterations of cellular homeostasis following SARS-CoV-2 infection and Spike protein exposureGioia Cappelletti, Lorenzo Brambilla, Sergio Strizzi, et al.
Cellular and Molecular Life Sciences : CMLS|December 26, 2024
Targeting STMN2 for neuroprotection and neuromuscular recovery in Spinal Muscular Atrophy: evidence from in vitro and in vivo SMA modelsElisa Pagliari, Michela Taiana, Paolo Manzini, et al.
Frontiers in Neurology|August 29, 2019
Ophthalmoplegia Due to Miller Fisher Syndrome in a Patient With Myasthenia GravisRoberta Brusa, Irene Faravelli, Delia Gagliardi, et al.
Biochimica Et Biophysica Acta|August 6, 2014
Glycogen storage disease type III: A novel Agl knockout mouse modelSerena Pagliarani, Sabrina Lucchiari, Gianna Ulzi, et al.
Pageof 29