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M Moggio

Showing results (31-40 of 121) with videos related to

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Lancet (London, England)|July 25, 1987
Muscle G6PD deficiencyN Bresolin, L Bet, M Moggio, et al.
Acta Neuropathologica|January 1, 1992
Sural nerve immunoreactivity for nerve growth factor receptor in a case of localized hypertrophic neuropathyM Sciacco, E Scarpini, P L Baron, et al.
Journal of Neurology|December 1, 1989
Rapid quantitative immunohistochemical assessment of human peripheral neuropathies using a monoclonal antibody against nerve growth factor receptorE Scarpini, S Beretta, A H Ross, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 1, 1983
Discordant HLA haplotype segregation in a family with progressive extrinsic ophthalmoplegia and ragged red fibresR Scorza Smeraldi, G Fabio, M Vanoli, et al.
Biochemical Society Transactions|August 1, 1985
Cytochrome c oxidase deficiencyS DiMauro, M Zeviani, E Bonilla, et al.
Journal of Neurology|February 1, 1992
Dystrophin deficiency in a case of congenital myopathyA Prelle, R Medori, M Moggio, et al.
Neurology|August 1, 1991
Dystrophin deficiency in young girls with sporadic myopathy and normal karyotypeC Minetti, H W Chang, R Medori, et al.
Journal of the Neurological Sciences|July 1, 1993
Multiple deletions of mitochondrial DNA in a patient with periodic attacks of paralysisA Prelle, M Moggio, N Checcarelli, et al.
Muscle & Nerve|November 1, 1989
Ultrastructural localization of calcium binding sites on human muscle cell surfaceM Moggio, S Jann, L Adobbati, et al.
Acta Neuropathologica|January 1, 1995
High serum creatine kinase levels associated with cylindrical spirals at muscle biopsyS Rapuzzi, A Prelle, M Moggio, et al.
Pageof 13

Showing results (31-40 of 121) with videos related to

Sort By:
Pageof 13
Lancet (London, England)|July 25, 1987
Muscle G6PD deficiencyN Bresolin, L Bet, M Moggio, et al.
Acta Neuropathologica|January 1, 1992
Sural nerve immunoreactivity for nerve growth factor receptor in a case of localized hypertrophic neuropathyM Sciacco, E Scarpini, P L Baron, et al.
Journal of Neurology|December 1, 1989
Rapid quantitative immunohistochemical assessment of human peripheral neuropathies using a monoclonal antibody against nerve growth factor receptorE Scarpini, S Beretta, A H Ross, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 1, 1983
Discordant HLA haplotype segregation in a family with progressive extrinsic ophthalmoplegia and ragged red fibresR Scorza Smeraldi, G Fabio, M Vanoli, et al.
Biochemical Society Transactions|August 1, 1985
Cytochrome c oxidase deficiencyS DiMauro, M Zeviani, E Bonilla, et al.
Journal of Neurology|February 1, 1992
Dystrophin deficiency in a case of congenital myopathyA Prelle, R Medori, M Moggio, et al.
Neurology|August 1, 1991
Dystrophin deficiency in young girls with sporadic myopathy and normal karyotypeC Minetti, H W Chang, R Medori, et al.
Journal of the Neurological Sciences|July 1, 1993
Multiple deletions of mitochondrial DNA in a patient with periodic attacks of paralysisA Prelle, M Moggio, N Checcarelli, et al.
Muscle & Nerve|November 1, 1989
Ultrastructural localization of calcium binding sites on human muscle cell surfaceM Moggio, S Jann, L Adobbati, et al.
Acta Neuropathologica|January 1, 1995
High serum creatine kinase levels associated with cylindrical spirals at muscle biopsyS Rapuzzi, A Prelle, M Moggio, et al.
Pageof 13