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A Prelle

Showing results (41-50 of 84) with videos related to

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International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|January 1, 1991
Appearance and localization of dystrophin in normal human fetal muscleA Prelle, L Chianese, M Moggio, et al.
Journal of the Peripheral Nervous System : JPNS|July 25, 2000
Severe polyneuropathy in a patient with Churg-Strauss syndromeP Bazzi, L Tancredi, E Scarpini, 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.
Neuropediatrics|February 1, 1992
Congenital myopathy with type 2A muscle fiber uniformity and smallnessA Gallanti, A Prelle, L Chianese, et al.
Cerebral Cortex (New York, N.Y. : 1991)|March 4, 2011
Sensorimotor functional connectivity changes in amyotrophic lateral sclerosisF Agosta, P Valsasina, M Absinta, 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.
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.
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.
Pageof 9

Showing results (41-50 of 84) with videos related to

Sort By:
Pageof 9
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|January 1, 1991
Appearance and localization of dystrophin in normal human fetal muscleA Prelle, L Chianese, M Moggio, et al.
Journal of the Peripheral Nervous System : JPNS|July 25, 2000
Severe polyneuropathy in a patient with Churg-Strauss syndromeP Bazzi, L Tancredi, E Scarpini, 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.
Neuropediatrics|February 1, 1992
Congenital myopathy with type 2A muscle fiber uniformity and smallnessA Gallanti, A Prelle, L Chianese, et al.
Cerebral Cortex (New York, N.Y. : 1991)|March 4, 2011
Sensorimotor functional connectivity changes in amyotrophic lateral sclerosisF Agosta, P Valsasina, M Absinta, 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.
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.
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.
Pageof 9