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Sabrina Sacconi

Showing results (1-10 of 156) with videos related to

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Journal of Human Genetics|April 18, 2009
Mutation analysis of COX18 in 29 patients with isolated cytochrome c oxidase deficiencySabrina Sacconi, Leonardo Salviati, Eva Trevisson
Biochimica Et Biophysica Acta|June 3, 2014
Facioscapulohumeral muscular dystrophySabrina Sacconi, Leonardo Salviati, Claude Desnuelle
Expert Review of Neurotherapeutics|September 17, 2020
Diagnostic challenges in metabolic myopathiesCorrado Angelini, Roberta Marozzo, Valentina Pegoraro, et al.
Journal of Neurology|January 26, 2017
Long term follow-up of cerebrovascular abnormalities in late onset Pompe disease (LOPD)Matteo Garibaldi, Sabrina Sacconi, Giovanni Antonini, et al.
BMC Neurology|July 23, 2018
Miller Fisher syndrome, Bickerstaff brainstem encephalitis and Guillain-Barré syndrome overlap with persistent non-demyelinating conduction blocks: a case reportAngela Puma, Jeanne Benoit, Sabrina Sacconi, et al.
Stem Cells and Development|November 18, 2015
Modeling Andersen's Syndrome in Human Induced Pluripotent Stem CellsJonathan Pini, Matthieu Rouleau, Claude Desnuelle, et al.
Medecine Sciences : M/S|April 4, 2019
[E-Health and therapeutic innovation]Sabrina Sacconi, Judith Mehl, Claire Lenain, et al.
Neuropediatrics|October 27, 2025
Nerve Ultrasound in Pediatric Polyneuropathies: A Systematic ReviewSimona Maccora, Vincenzo Di Stefano, Filippo Brighina, et al.
Neurology and Therapy|May 5, 2022
The European Lambert-Eaton Myasthenic Syndrome Registry: Long-Term Outcomes Following Symptomatic TreatmentAndreas Meisel, Jörn P Sieb, Gwendal Le Masson, et al.
Bulletin De L'Academie Nationale De Medecine|October 26, 2005
[The possible place of autologus cell therapy in facioscapulohumeral muscular dystrophy]Claude Desnuelle, Sabrina Sacconi, Jean-Pierre Marolleau, et al.
Pageof 16

Showing results (1-10 of 156) with videos related to

Sort By:
Pageof 16
Journal of Human Genetics|April 18, 2009
Mutation analysis of COX18 in 29 patients with isolated cytochrome c oxidase deficiencySabrina Sacconi, Leonardo Salviati, Eva Trevisson
Biochimica Et Biophysica Acta|June 3, 2014
Facioscapulohumeral muscular dystrophySabrina Sacconi, Leonardo Salviati, Claude Desnuelle
Expert Review of Neurotherapeutics|September 17, 2020
Diagnostic challenges in metabolic myopathiesCorrado Angelini, Roberta Marozzo, Valentina Pegoraro, et al.
Journal of Neurology|January 26, 2017
Long term follow-up of cerebrovascular abnormalities in late onset Pompe disease (LOPD)Matteo Garibaldi, Sabrina Sacconi, Giovanni Antonini, et al.
BMC Neurology|July 23, 2018
Miller Fisher syndrome, Bickerstaff brainstem encephalitis and Guillain-Barré syndrome overlap with persistent non-demyelinating conduction blocks: a case reportAngela Puma, Jeanne Benoit, Sabrina Sacconi, et al.
Stem Cells and Development|November 18, 2015
Modeling Andersen's Syndrome in Human Induced Pluripotent Stem CellsJonathan Pini, Matthieu Rouleau, Claude Desnuelle, et al.
Medecine Sciences : M/S|April 4, 2019
[E-Health and therapeutic innovation]Sabrina Sacconi, Judith Mehl, Claire Lenain, et al.
Neuropediatrics|October 27, 2025
Nerve Ultrasound in Pediatric Polyneuropathies: A Systematic ReviewSimona Maccora, Vincenzo Di Stefano, Filippo Brighina, et al.
Neurology and Therapy|May 5, 2022
The European Lambert-Eaton Myasthenic Syndrome Registry: Long-Term Outcomes Following Symptomatic TreatmentAndreas Meisel, Jörn P Sieb, Gwendal Le Masson, et al.
Bulletin De L'Academie Nationale De Medecine|October 26, 2005
[The possible place of autologus cell therapy in facioscapulohumeral muscular dystrophy]Claude Desnuelle, Sabrina Sacconi, Jean-Pierre Marolleau, et al.
Pageof 16