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A Prelle

Showing results (11-20 of 84) with videos related to

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Muscle & Nerve|May 1, 1994
Anionic phospholipids calcium binding sites in Duchenne and murine X-linked muscular dystrophyM Moggio, A Prelle, G Fagiolari, et al.
Annals of Neurology|July 1, 1990
Tissue distribution and transmission of mitochondrial DNA deletions in mitochondrial myopathiesM Zeviani, C Gellera, M Pannacci, et al.
Journal of Neurology|February 1, 1992
Dystrophin deficiency in a case of congenital myopathyA Prelle, R Medori, M Moggio, et al.
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.
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 Neurology, Neurosurgery, and Psychiatry|October 13, 2006
Diffusion anisotropy of the cervical cord is strictly associated with disability in amyotrophic lateral sclerosisP Valsasina, F Agosta, B Benedetti, 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.
Journal of Neurology|September 1, 1995
Early-onset encephalomyopathy associated with tissue-specific mitochondrial DNA depletion: a morphological, biochemical and molecular-genetic studyC Mariotti, G Uziel, F Carrara, et al.
Annals of the New York Academy of Sciences|January 1, 1986
Cytochrome oxidase deficiency: clinical and biochemical heterogeneityS DiMauro, M Zeviani, S Servidei, et al.
Advances in Neurology|January 1, 1988
Biochemical and molecular aspects of cytochrome C oxidase deficiencyS DiMauro, M Zeviani, S Servidei, et al.
Pageof 9

Showing results (11-20 of 84) with videos related to

Sort By:
Pageof 9
Muscle & Nerve|May 1, 1994
Anionic phospholipids calcium binding sites in Duchenne and murine X-linked muscular dystrophyM Moggio, A Prelle, G Fagiolari, et al.
Annals of Neurology|July 1, 1990
Tissue distribution and transmission of mitochondrial DNA deletions in mitochondrial myopathiesM Zeviani, C Gellera, M Pannacci, et al.
Journal of Neurology|February 1, 1992
Dystrophin deficiency in a case of congenital myopathyA Prelle, R Medori, M Moggio, et al.
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.
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 Neurology, Neurosurgery, and Psychiatry|October 13, 2006
Diffusion anisotropy of the cervical cord is strictly associated with disability in amyotrophic lateral sclerosisP Valsasina, F Agosta, B Benedetti, 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.
Journal of Neurology|September 1, 1995
Early-onset encephalomyopathy associated with tissue-specific mitochondrial DNA depletion: a morphological, biochemical and molecular-genetic studyC Mariotti, G Uziel, F Carrara, et al.
Annals of the New York Academy of Sciences|January 1, 1986
Cytochrome oxidase deficiency: clinical and biochemical heterogeneityS DiMauro, M Zeviani, S Servidei, et al.
Advances in Neurology|January 1, 1988
Biochemical and molecular aspects of cytochrome C oxidase deficiencyS DiMauro, M Zeviani, S Servidei, et al.
Pageof 9