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Paola Rinchetti

Showing results (1-10 of 17) with videos related to

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Molecular Neurobiology|April 20, 2017
MicroRNA Metabolism and Dysregulation in Amyotrophic Lateral SclerosisPaola Rinchetti, Mafalda Rizzuti, Irene Faravelli, et al.
Frontiers in Cellular Neuroscience|March 6, 2023
SMN post-translational modifications in spinal muscular atrophyGiulietta M Riboldi, Irene Faravelli, Paola Rinchetti, et al.
International Journal of Molecular Sciences|February 11, 2023
The SMN Complex at the Crossroad between RNA Metabolism and NeurodegenerationIrene Faravelli, Giulietta M Riboldi, Paola Rinchetti, et al.
Journal of Cellular and Molecular Medicine|June 23, 2015
Clinical and molecular features and therapeutic perspectives of spinal muscular atrophy with respiratory distress type 1Fiammetta Vanoli, Paola Rinchetti, Francesca Porro, et al.
International Journal of Molecular Sciences|May 27, 2023
Brain Calcifications: Genetic, Molecular, and Clinical AspectsEdoardo Monfrini, Federica Arienti, Paola Rinchetti, et al.
Stem Cell Research & Therapy|August 27, 2014
Motor neuron derivation from human embryonic and induced pluripotent stem cells: experimental approaches and clinical perspectivesIrene Faravelli, Monica Bucchia, Paola Rinchetti, et al.
Cellular and Molecular Life Sciences : CMLS|December 19, 2015
Is spinal muscular atrophy a disease of the motor neurons only: pathogenesis and therapeutic implications?Chiara Simone, Agnese Ramirez, Monica Bucchia, et al.
Journal of the Neurological Sciences|September 25, 2014
The wide spectrum of clinical phenotypes of spinal muscular atrophy with respiratory distress type 1: a systematic reviewFrancesca Porro, Paola Rinchetti, Francesca Magri, et al.
Science Advances|November 25, 2015
Gene therapy rescues disease phenotype in a spinal muscular atrophy with respiratory distress type 1 (SMARD1) mouse modelMonica Nizzardo, Chiara Simone, Federica Rizzo, et al.
Parkinsonism & Related Disorders|March 10, 2019
Neurofascin (NFASC) gene mutation causes autosomal recessive ataxia with demyelinating neuropathyEdoardo Monfrini, Letizia Straniero, Sara Bonato, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Molecular Neurobiology|April 20, 2017
MicroRNA Metabolism and Dysregulation in Amyotrophic Lateral SclerosisPaola Rinchetti, Mafalda Rizzuti, Irene Faravelli, et al.
Frontiers in Cellular Neuroscience|March 6, 2023
SMN post-translational modifications in spinal muscular atrophyGiulietta M Riboldi, Irene Faravelli, Paola Rinchetti, et al.
International Journal of Molecular Sciences|February 11, 2023
The SMN Complex at the Crossroad between RNA Metabolism and NeurodegenerationIrene Faravelli, Giulietta M Riboldi, Paola Rinchetti, et al.
Journal of Cellular and Molecular Medicine|June 23, 2015
Clinical and molecular features and therapeutic perspectives of spinal muscular atrophy with respiratory distress type 1Fiammetta Vanoli, Paola Rinchetti, Francesca Porro, et al.
International Journal of Molecular Sciences|May 27, 2023
Brain Calcifications: Genetic, Molecular, and Clinical AspectsEdoardo Monfrini, Federica Arienti, Paola Rinchetti, et al.
Stem Cell Research & Therapy|August 27, 2014
Motor neuron derivation from human embryonic and induced pluripotent stem cells: experimental approaches and clinical perspectivesIrene Faravelli, Monica Bucchia, Paola Rinchetti, et al.
Cellular and Molecular Life Sciences : CMLS|December 19, 2015
Is spinal muscular atrophy a disease of the motor neurons only: pathogenesis and therapeutic implications?Chiara Simone, Agnese Ramirez, Monica Bucchia, et al.
Journal of the Neurological Sciences|September 25, 2014
The wide spectrum of clinical phenotypes of spinal muscular atrophy with respiratory distress type 1: a systematic reviewFrancesca Porro, Paola Rinchetti, Francesca Magri, et al.
Science Advances|November 25, 2015
Gene therapy rescues disease phenotype in a spinal muscular atrophy with respiratory distress type 1 (SMARD1) mouse modelMonica Nizzardo, Chiara Simone, Federica Rizzo, et al.
Parkinsonism & Related Disorders|March 10, 2019
Neurofascin (NFASC) gene mutation causes autosomal recessive ataxia with demyelinating neuropathyEdoardo Monfrini, Letizia Straniero, Sara Bonato, et al.
Pageof 2