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Stefania Corti

Showing results (71-80 of 287) with videos related to

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Clinical Therapeutics|February 11, 2015
Therapeutic development in amyotrophic lateral sclerosisMonica Bucchia, Agnese Ramirez, Valeria Parente, et al.
Biomedicines|February 25, 2022
Targeting PTB for Glia-to-Neuron Reprogramming In Vitro and In Vivo for Therapeutic Development in Neurological DiseasesMatilde Contardo, Roberta De Gioia, Delia Gagliardi, et al.
Journal of the Neurological Sciences|July 4, 2009
Aphasic and visual aura with increased vasogenic leakage: an atypical migrainosus statusSilvia Lanfranconi, Stefania Corti, Anna Bersano, et al.
Frontiers in Neurology|December 6, 2024
Cardiac risk and myocardial fibrosis assessment with cardiac magnetic resonance in patients with myotonic dystrophyElena Abati, Claudia Alberti, Valentina Tambè, et al.
Therapeutic Advances in Neurological Disorders|May 21, 2019
Human induced pluripotent stem cell models for the study and treatment of Duchenne and Becker muscular dystrophiesDaniela Piga, Sabrina Salani, Francesca Magri, et al.
Cellular and Molecular Life Sciences : CMLS|April 5, 2014
Stem cell transplantation for amyotrophic lateral sclerosis: therapeutic potential and perspectives on clinical translationIrene Faravelli, Giulietta Riboldi, Monica Nizzardo, et al.
Journal of Cellular and Molecular Medicine|January 10, 2014
Molecular, genetic and stem cell-mediated therapeutic strategies for spinal muscular atrophy (SMA)Chiara Zanetta, Giulietta Riboldi, Monica Nizzardo, et al.
Neurology Research International|June 20, 2013
Mitochondrial fusion proteins and human diseasesMichela Ranieri, Simona Brajkovic, Giulietta Riboldi, et al.
BMC Neurology|August 4, 2014
A novel CCM1 mutation associated with multiple cerebral and vertebral cavernous malformationsSilvia Lanfranconi, Dario Ronchi, Naghia Ahmed, et al.
Frontiers in Neurology|March 14, 2022
Case Report: Thymidine Kinase 2 (TK2) Deficiency: A Novel Mutation Associated With Childhood-Onset Mitochondrial Myopathy and Atypical ProgressionArianna Manini, Megi Meneri, Carmelo Rodolico, et al.
Pageof 29

Showing results (71-80 of 287) with videos related to

Sort By:
Pageof 29
Clinical Therapeutics|February 11, 2015
Therapeutic development in amyotrophic lateral sclerosisMonica Bucchia, Agnese Ramirez, Valeria Parente, et al.
Biomedicines|February 25, 2022
Targeting PTB for Glia-to-Neuron Reprogramming In Vitro and In Vivo for Therapeutic Development in Neurological DiseasesMatilde Contardo, Roberta De Gioia, Delia Gagliardi, et al.
Journal of the Neurological Sciences|July 4, 2009
Aphasic and visual aura with increased vasogenic leakage: an atypical migrainosus statusSilvia Lanfranconi, Stefania Corti, Anna Bersano, et al.
Frontiers in Neurology|December 6, 2024
Cardiac risk and myocardial fibrosis assessment with cardiac magnetic resonance in patients with myotonic dystrophyElena Abati, Claudia Alberti, Valentina Tambè, et al.
Therapeutic Advances in Neurological Disorders|May 21, 2019
Human induced pluripotent stem cell models for the study and treatment of Duchenne and Becker muscular dystrophiesDaniela Piga, Sabrina Salani, Francesca Magri, et al.
Cellular and Molecular Life Sciences : CMLS|April 5, 2014
Stem cell transplantation for amyotrophic lateral sclerosis: therapeutic potential and perspectives on clinical translationIrene Faravelli, Giulietta Riboldi, Monica Nizzardo, et al.
Journal of Cellular and Molecular Medicine|January 10, 2014
Molecular, genetic and stem cell-mediated therapeutic strategies for spinal muscular atrophy (SMA)Chiara Zanetta, Giulietta Riboldi, Monica Nizzardo, et al.
Neurology Research International|June 20, 2013
Mitochondrial fusion proteins and human diseasesMichela Ranieri, Simona Brajkovic, Giulietta Riboldi, et al.
BMC Neurology|August 4, 2014
A novel CCM1 mutation associated with multiple cerebral and vertebral cavernous malformationsSilvia Lanfranconi, Dario Ronchi, Naghia Ahmed, et al.
Frontiers in Neurology|March 14, 2022
Case Report: Thymidine Kinase 2 (TK2) Deficiency: A Novel Mutation Associated With Childhood-Onset Mitochondrial Myopathy and Atypical ProgressionArianna Manini, Megi Meneri, Carmelo Rodolico, et al.
Pageof 29