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S Servidei

Showing results (41-50 of 146) with videos related to

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Clinical Neuropathology|May 1, 1986
Morphological studies of sural nerve biopsies in the pseudopolyneuropathic form of amyotrophic lateral sclerosisG di Trapani, P David, A La Cara, et al.
Neuromuscular Disorders : NMD|July 23, 1998
A late-onset mitochondrial myopathy is associated with a novel mitochondrial DNA (mtDNA) point mutation in the tRNA(Trp) geneG Silvestri, M Rana, A DiMuzio, et al.
Acta Neurologica|December 1, 1982
Muscular and cerebral involvement in a familiar mitochondrial diseaseM L Vaccario, M Lo Monaco, S Servidei, et al.
Molecular and Cellular Neurosciences|April 21, 2001
Apoptosis and ROS detoxification enzymes correlate with cytochrome c oxidase deficiency in mitochondrial encephalomyopathiesS Di Giovanni, M Mirabella, M Papacci, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 11, 2000
An Italian family with autosomal recessive quadriceps-sparing inclusion-body myopathy (ARQS-IBM) linked to chromosome 9p1M Mirabella, K Christodoulou, S Di Giovanni, et al.
Neurology|June 1, 1987
Cardiomyopathy, mental retardation, and autophagic vacuolar myopathyZ H Hart, S Servidei, P L Peterson, et al.
Brain Pathology (Zurich, Switzerland)|April 1, 1992
Disorders associated with depletion of mitochondrial DNAE Ricci, C T Moraes, S Servidei, et al.
Neurology|June 9, 2004
Incomplete penetrance in an SPG3A-linked family with a new mutation in the atlastin geneA D'Amico, A Tessa, A Sabino, et al.
Clinical Neuropathology|May 15, 2002
MERRF/MELAS overlap syndrome in a family with A3243G mtDNA mutationT Mongini, C Doriguzzi, L Chiadò-Piat, et al.
Clinical Neuropathology|July 1, 1997
Mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS)G Di Trapani, B Gregori, S Servidei, et al.
Pageof 15

Showing results (41-50 of 146) with videos related to

Sort By:
Pageof 15
Clinical Neuropathology|May 1, 1986
Morphological studies of sural nerve biopsies in the pseudopolyneuropathic form of amyotrophic lateral sclerosisG di Trapani, P David, A La Cara, et al.
Neuromuscular Disorders : NMD|July 23, 1998
A late-onset mitochondrial myopathy is associated with a novel mitochondrial DNA (mtDNA) point mutation in the tRNA(Trp) geneG Silvestri, M Rana, A DiMuzio, et al.
Acta Neurologica|December 1, 1982
Muscular and cerebral involvement in a familiar mitochondrial diseaseM L Vaccario, M Lo Monaco, S Servidei, et al.
Molecular and Cellular Neurosciences|April 21, 2001
Apoptosis and ROS detoxification enzymes correlate with cytochrome c oxidase deficiency in mitochondrial encephalomyopathiesS Di Giovanni, M Mirabella, M Papacci, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 11, 2000
An Italian family with autosomal recessive quadriceps-sparing inclusion-body myopathy (ARQS-IBM) linked to chromosome 9p1M Mirabella, K Christodoulou, S Di Giovanni, et al.
Neurology|June 1, 1987
Cardiomyopathy, mental retardation, and autophagic vacuolar myopathyZ H Hart, S Servidei, P L Peterson, et al.
Brain Pathology (Zurich, Switzerland)|April 1, 1992
Disorders associated with depletion of mitochondrial DNAE Ricci, C T Moraes, S Servidei, et al.
Neurology|June 9, 2004
Incomplete penetrance in an SPG3A-linked family with a new mutation in the atlastin geneA D'Amico, A Tessa, A Sabino, et al.
Clinical Neuropathology|May 15, 2002
MERRF/MELAS overlap syndrome in a family with A3243G mtDNA mutationT Mongini, C Doriguzzi, L Chiadò-Piat, et al.
Clinical Neuropathology|July 1, 1997
Mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS)G Di Trapani, B Gregori, S Servidei, et al.
Pageof 15