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L Bet

Showing results (11-20 of 23) with videos related to

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Journal of the Neurological Sciences|May 1, 1990
Kearns-Sayre syndrome: different amounts of deleted mitochondrial DNA are present in several autoptic tissuesC Ponzetto, N Bresolin, A Bordoni, et al.
European Neurology|January 1, 1992
Lipid storage myopathy in multiple acyl-CoA dehydrogenase deficiency: an adult caseT Mongini, C Doriguzzi, L Palmucci, et al.
Neurology|June 1, 1988
Clinical and biochemical correlations in mitochondrial myopathies treated with coenzyme Q10N Bresolin, L Bet, A Binda, et al.
Neurology|October 1, 1987
Biochemical and immunologic studies in a case of congenital myopathy with unusual morphologic featuresD Biral, E Damiani, E Scarpini, et al.
Journal of Neurology|May 1, 1989
Muscle glucose-6-phosphate dehydrogenase deficiencyN Bresolin, L Bet, M Moggio, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|January 1, 1989
Cytochrome c oxidase during human fetal developmentM Moggio, N Bresolin, E Scarpini, 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.
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 Neurology|July 1, 1994
Multiple sclerosis and mitochondrial myopathy: an unusual combination of diseasesL Bet, M Moggio, G P Comi, et al.
Journal of Neurology|March 1, 1995
Early-onset cerebellar ataxia, myoclonus and hypogonadism in a case of mitochondrial complex III deficiency treated with vitamins K3 and CA Toscano, M C Fazio, G Vita, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Journal of the Neurological Sciences|May 1, 1990
Kearns-Sayre syndrome: different amounts of deleted mitochondrial DNA are present in several autoptic tissuesC Ponzetto, N Bresolin, A Bordoni, et al.
European Neurology|January 1, 1992
Lipid storage myopathy in multiple acyl-CoA dehydrogenase deficiency: an adult caseT Mongini, C Doriguzzi, L Palmucci, et al.
Neurology|June 1, 1988
Clinical and biochemical correlations in mitochondrial myopathies treated with coenzyme Q10N Bresolin, L Bet, A Binda, et al.
Neurology|October 1, 1987
Biochemical and immunologic studies in a case of congenital myopathy with unusual morphologic featuresD Biral, E Damiani, E Scarpini, et al.
Journal of Neurology|May 1, 1989
Muscle glucose-6-phosphate dehydrogenase deficiencyN Bresolin, L Bet, M Moggio, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|January 1, 1989
Cytochrome c oxidase during human fetal developmentM Moggio, N Bresolin, E Scarpini, 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.
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 Neurology|July 1, 1994
Multiple sclerosis and mitochondrial myopathy: an unusual combination of diseasesL Bet, M Moggio, G P Comi, et al.
Journal of Neurology|March 1, 1995
Early-onset cerebellar ataxia, myoclonus and hypogonadism in a case of mitochondrial complex III deficiency treated with vitamins K3 and CA Toscano, M C Fazio, G Vita, et al.
Pageof 3