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G Scarlato

Showing results (151-160 of 234) with videos related to

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Neurology|June 1, 1988
Clinical and biochemical correlations in mitochondrial myopathies treated with coenzyme Q10N Bresolin, L Bet, A Binda, et al.
Journal of the Neurological Sciences|May 1, 1994
Multiple deletions of mitochondrial DNA in sporadic and atypical cases of encephalomyopathyN Checcarelli, A Prelle, M Moggio, 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.
Human Mutation|November 21, 2002
Molecular characterisation of GSD III subjects and identification of six novel mutations in AGLS Lucchiari, M A Donati, R Parini, et al.
Journal of Neurology|December 1, 1991
The natural history and results of surgery in 50 cases of syringomyeliaC Mariani, M G Cislaghi, S Barbieri, et al.
Neuroscience Letters|October 29, 1993
Myelin protein transcripts increase in experimental diabetic neuropathyA M Conti, M L Malosio, E Scarpini, et al.
Brain : a Journal of Neurology|January 29, 2000
Synergistic effect of beta-amyloid protein and interferon gamma on nitric oxide production by C2C12 muscle cellsP Baron, D Galimberti, L Meda, et al.
Journal of Neurology|February 1, 1995
Ryanodine receptor gene point mutation and malignant hyperthermia susceptibilityI Moroni, E F Gonano, G P Comi, et al.
Journal of the Neurological Sciences|May 1, 1994
Chronic progressive external ophthalmoplegia: a correlative study of quantitative molecular data and histochemical and biochemical profileA Fassati, A Bordoni, P Amboni, et al.
Applied Neurophysiology|January 1, 1988
Primary cultures of human caudate nucleusV Silani, G Pezzoli, E Motti, et al.
Pageof 24

Showing results (151-160 of 234) with videos related to

Sort By:
Pageof 24
Neurology|June 1, 1988
Clinical and biochemical correlations in mitochondrial myopathies treated with coenzyme Q10N Bresolin, L Bet, A Binda, et al.
Journal of the Neurological Sciences|May 1, 1994
Multiple deletions of mitochondrial DNA in sporadic and atypical cases of encephalomyopathyN Checcarelli, A Prelle, M Moggio, 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.
Human Mutation|November 21, 2002
Molecular characterisation of GSD III subjects and identification of six novel mutations in AGLS Lucchiari, M A Donati, R Parini, et al.
Journal of Neurology|December 1, 1991
The natural history and results of surgery in 50 cases of syringomyeliaC Mariani, M G Cislaghi, S Barbieri, et al.
Neuroscience Letters|October 29, 1993
Myelin protein transcripts increase in experimental diabetic neuropathyA M Conti, M L Malosio, E Scarpini, et al.
Brain : a Journal of Neurology|January 29, 2000
Synergistic effect of beta-amyloid protein and interferon gamma on nitric oxide production by C2C12 muscle cellsP Baron, D Galimberti, L Meda, et al.
Journal of Neurology|February 1, 1995
Ryanodine receptor gene point mutation and malignant hyperthermia susceptibilityI Moroni, E F Gonano, G P Comi, et al.
Journal of the Neurological Sciences|May 1, 1994
Chronic progressive external ophthalmoplegia: a correlative study of quantitative molecular data and histochemical and biochemical profileA Fassati, A Bordoni, P Amboni, et al.
Applied Neurophysiology|January 1, 1988
Primary cultures of human caudate nucleusV Silani, G Pezzoli, E Motti, et al.
Pageof 24