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S Servidei

Showing results (21-30 of 146) with videos related to

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Italian Journal of Neurological Sciences|December 1, 1984
Clinical study of proximal spinal muscular atrophy. Report on 89 casesP Tonali, S Servidei, A Uncini, et al.
Neurology|January 1, 1987
Benign reversible muscle cytochrome c oxidase deficiency: a second caseM Zeviani, P Peterson, S Servidei, et al.
Experimental and Molecular Pathology|March 27, 2001
Deletion polymorphism of DNASE1L1, an X-linked DNase I-like gene, in acid maltase deficiency disordersG Malferrari, M Mirabella, Y D'Alessandra, et al.
Neurology|September 20, 2000
Apoptotic features accompany acute quadriplegic myopathyS Di Giovanni, M Mirabella, A D'Amico, et al.
Journal of the Neurological Sciences|October 1, 1992
Somatosensory and motor evoked potentials in the assessment of cerebrotendinous xanthomatosis before and after treatment with chenodeoxycholic acid: a preliminary studyD Restuccia, V Di Lazzaro, S Servidei, et al.
European Review for Medical and Pharmacological Sciences|July 20, 2018
Nutritional support in mitochondrial diseases: the state of the artE Rinninella, M Pizzoferrato, M Cintoni, et al.
Brain : a Journal of Neurology|December 28, 1999
Apoptosis in mitochondrial encephalomyopathies with mitochondrial DNA mutations: a potential pathogenic mechanismM Mirabella, S Di Giovanni, G Silvestri, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 18, 2003
Immunohistochemical study of caveolin-3 in idiopathic hyperCKaemiaM Capasso, S Lupo, A Di Muzio, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 1, 1993
Ocular myasthenia: diagnostic value of single fibre EMG in the orbicularis oculi muscleM Milone, M L Monaco, A Evoli, et al.
Archives of Neurology|September 1, 1986
Mitochondrial myopathy due to complex III deficiency with normal reducible cytochrome b concentrationH Reichmann, R Rohkamm, M Zeviani, et al.
Pageof 15

Showing results (21-30 of 146) with videos related to

Sort By:
Pageof 15
Italian Journal of Neurological Sciences|December 1, 1984
Clinical study of proximal spinal muscular atrophy. Report on 89 casesP Tonali, S Servidei, A Uncini, et al.
Neurology|January 1, 1987
Benign reversible muscle cytochrome c oxidase deficiency: a second caseM Zeviani, P Peterson, S Servidei, et al.
Experimental and Molecular Pathology|March 27, 2001
Deletion polymorphism of DNASE1L1, an X-linked DNase I-like gene, in acid maltase deficiency disordersG Malferrari, M Mirabella, Y D'Alessandra, et al.
Neurology|September 20, 2000
Apoptotic features accompany acute quadriplegic myopathyS Di Giovanni, M Mirabella, A D'Amico, et al.
Journal of the Neurological Sciences|October 1, 1992
Somatosensory and motor evoked potentials in the assessment of cerebrotendinous xanthomatosis before and after treatment with chenodeoxycholic acid: a preliminary studyD Restuccia, V Di Lazzaro, S Servidei, et al.
European Review for Medical and Pharmacological Sciences|July 20, 2018
Nutritional support in mitochondrial diseases: the state of the artE Rinninella, M Pizzoferrato, M Cintoni, et al.
Brain : a Journal of Neurology|December 28, 1999
Apoptosis in mitochondrial encephalomyopathies with mitochondrial DNA mutations: a potential pathogenic mechanismM Mirabella, S Di Giovanni, G Silvestri, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 18, 2003
Immunohistochemical study of caveolin-3 in idiopathic hyperCKaemiaM Capasso, S Lupo, A Di Muzio, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 1, 1993
Ocular myasthenia: diagnostic value of single fibre EMG in the orbicularis oculi muscleM Milone, M L Monaco, A Evoli, et al.
Archives of Neurology|September 1, 1986
Mitochondrial myopathy due to complex III deficiency with normal reducible cytochrome b concentrationH Reichmann, R Rohkamm, M Zeviani, et al.
Pageof 15