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M Moggio

Showing results (71-80 of 121) with videos related to

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Neuropediatrics|February 1, 1992
Congenital myopathy with type 2A muscle fiber uniformity and smallnessA Gallanti, A Prelle, L Chianese, et al.
Journal of Neurology|November 1, 1990
A case of mitochondrial myopathy, lactic acidosis and complex I deficiencyL Bet, N Bresolin, M Moggio, et al.
Acta Neuropathologica|January 1, 1994
Mitochondrial myopathy: correlation between oxidative defect and mitochondrial DNA deletions at single fiber levelA Prelle, G Fagiolari, N Checcarelli, et al.
Annals of Neurology|October 1, 1989
Anti-myelin-associated glycoprotein IgM antibody titers in neuropathy associated with macroglobulinemiaE Nobile-Orazio, E Francomano, R Daverio, et al.
Journal of Neurology|July 1, 1994
Multiple sclerosis and mitochondrial myopathy: an unusual combination of diseasesL Bet, M Moggio, G P Comi, et al.
Annals of Neurology|June 1, 1987
Progressive cytochrome c oxidase deficiency in a case of Kearns-Sayre syndrome: morphological, immunological, and biochemical studies in muscle biopsies and autopsy tissuesN Bresolin, M Moggio, L Bet, et al.
Journal of the Neurological Sciences|September 1, 1996
Asymptomatic familial hyperCKemia associated with desmin accumulation in skeletal muscleA Prelle, C Rigoletto, M Moggio, et al.
Brain : a Journal of Neurology|February 1, 1994
Clinical variability in Becker muscular dystrophy. Genetic, biochemical and immunohistochemical correlatesG P Comi, A Prelle, N Bresolin, et al.
Neurology Research International|December 29, 2010
IgD Multiple Myeloma Paraproteinemia as a Cause of MyositisI Colombo, M E Fruguglietti, L Napoli, et al.
Neuromuscular Disorders : NMD|May 23, 2001
Primary beta-sarcoglycanopathy manifesting as recurrent exercise-induced myoglobinuriaR Cagliani, G P Comi, L Tancredi, et al.
Pageof 13

Showing results (71-80 of 121) with videos related to

Sort By:
Pageof 13
Neuropediatrics|February 1, 1992
Congenital myopathy with type 2A muscle fiber uniformity and smallnessA Gallanti, A Prelle, L Chianese, et al.
Journal of Neurology|November 1, 1990
A case of mitochondrial myopathy, lactic acidosis and complex I deficiencyL Bet, N Bresolin, M Moggio, et al.
Acta Neuropathologica|January 1, 1994
Mitochondrial myopathy: correlation between oxidative defect and mitochondrial DNA deletions at single fiber levelA Prelle, G Fagiolari, N Checcarelli, et al.
Annals of Neurology|October 1, 1989
Anti-myelin-associated glycoprotein IgM antibody titers in neuropathy associated with macroglobulinemiaE Nobile-Orazio, E Francomano, R Daverio, et al.
Journal of Neurology|July 1, 1994
Multiple sclerosis and mitochondrial myopathy: an unusual combination of diseasesL Bet, M Moggio, G P Comi, et al.
Annals of Neurology|June 1, 1987
Progressive cytochrome c oxidase deficiency in a case of Kearns-Sayre syndrome: morphological, immunological, and biochemical studies in muscle biopsies and autopsy tissuesN Bresolin, M Moggio, L Bet, et al.
Journal of the Neurological Sciences|September 1, 1996
Asymptomatic familial hyperCKemia associated with desmin accumulation in skeletal muscleA Prelle, C Rigoletto, M Moggio, et al.
Brain : a Journal of Neurology|February 1, 1994
Clinical variability in Becker muscular dystrophy. Genetic, biochemical and immunohistochemical correlatesG P Comi, A Prelle, N Bresolin, et al.
Neurology Research International|December 29, 2010
IgD Multiple Myeloma Paraproteinemia as a Cause of MyositisI Colombo, M E Fruguglietti, L Napoli, et al.
Neuromuscular Disorders : NMD|May 23, 2001
Primary beta-sarcoglycanopathy manifesting as recurrent exercise-induced myoglobinuriaR Cagliani, G P Comi, L Tancredi, et al.
Pageof 13