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Leda Volpi

Showing results (1-10 of 11) with videos related to

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Bioscience Reports|May 12, 2007
Functional diagnostics in mitochondrial diseasesGabriele Siciliano, Leda Volpi, Selina Piazza, et al.
Muscle & Nerve|September 29, 2011
Muscle metabolic alterations assessed by 31-phosphorus magnetic resonance spectroscopy in mild Becker muscular dystrophyMichela Tosetti, Stefania Linsalata, Roberta Battini, et al.
Neuromuscular Disorders : NMD|January 17, 2012
Rippling muscle disease and facioscapulohumeral dystrophy-like phenotype in a patient carrying a heterozygous CAV3 T78M mutation and a D4Z4 partial deletion: Further evidence for "double trouble" overlapping syndromesGiulia Ricci, Isabella Scionti, Greta Alì, et al.
American Journal of Alzheimer'S Disease and Other Dementias|September 22, 2017
Oxidative Stress Assessment in Alzheimer's Disease: A Clinic Setting StudyAndrea Vergallo, Linda Giampietri, Filippo Baldacci, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 14, 2011
Nerve and muscle involvement in mitochondrial disorders: an electrophysiological studyMichelangelo Mancuso, Selina Piazza, Leda Volpi, et al.
Orphanet Journal of Rare Diseases|April 6, 2016
Disease awareness in myotonic dystrophy type 1: an observational cross-sectional studySigrid Baldanzi, Francesca Bevilacqua, Rita Lorio, et al.
Sleep Medicine|August 24, 2015
Non-rapid eye movement sleep instability in mild cognitive impairment: a pilot studyMichelangelo Maestri, Luca Carnicelli, Gloria Tognoni, et al.
The European Journal of Neuroscience|April 4, 2017
Olfactory evaluation in Mild Cognitive Impairment: correlation with neurocognitive performance and endothelial functionAlessandro Tonacci, Rosa M Bruno, Lorenzo Ghiadoni, et al.
Clinical Biochemistry|August 10, 2010
Serum gamma-glutamyltransferase fractions in myotonic dystrophy type I: differences with healthy subjects and patients with liver diseaseMaria Franzini, Irene Fornaciari, Gabriele Siciliano, et al.
Psychiatry Research. Neuroimaging|December 13, 2018
Functional magnetic resonance imaging with encoding task in patients with mild cognitive impairment and different severity of leukoaraiosisAlberto Chiti, Paolo Cecchi, Ilaria Pesaresi, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Bioscience Reports|May 12, 2007
Functional diagnostics in mitochondrial diseasesGabriele Siciliano, Leda Volpi, Selina Piazza, et al.
Muscle & Nerve|September 29, 2011
Muscle metabolic alterations assessed by 31-phosphorus magnetic resonance spectroscopy in mild Becker muscular dystrophyMichela Tosetti, Stefania Linsalata, Roberta Battini, et al.
Neuromuscular Disorders : NMD|January 17, 2012
Rippling muscle disease and facioscapulohumeral dystrophy-like phenotype in a patient carrying a heterozygous CAV3 T78M mutation and a D4Z4 partial deletion: Further evidence for "double trouble" overlapping syndromesGiulia Ricci, Isabella Scionti, Greta Alì, et al.
American Journal of Alzheimer'S Disease and Other Dementias|September 22, 2017
Oxidative Stress Assessment in Alzheimer's Disease: A Clinic Setting StudyAndrea Vergallo, Linda Giampietri, Filippo Baldacci, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 14, 2011
Nerve and muscle involvement in mitochondrial disorders: an electrophysiological studyMichelangelo Mancuso, Selina Piazza, Leda Volpi, et al.
Orphanet Journal of Rare Diseases|April 6, 2016
Disease awareness in myotonic dystrophy type 1: an observational cross-sectional studySigrid Baldanzi, Francesca Bevilacqua, Rita Lorio, et al.
Sleep Medicine|August 24, 2015
Non-rapid eye movement sleep instability in mild cognitive impairment: a pilot studyMichelangelo Maestri, Luca Carnicelli, Gloria Tognoni, et al.
The European Journal of Neuroscience|April 4, 2017
Olfactory evaluation in Mild Cognitive Impairment: correlation with neurocognitive performance and endothelial functionAlessandro Tonacci, Rosa M Bruno, Lorenzo Ghiadoni, et al.
Clinical Biochemistry|August 10, 2010
Serum gamma-glutamyltransferase fractions in myotonic dystrophy type I: differences with healthy subjects and patients with liver diseaseMaria Franzini, Irene Fornaciari, Gabriele Siciliano, et al.
Psychiatry Research. Neuroimaging|December 13, 2018
Functional magnetic resonance imaging with encoding task in patients with mild cognitive impairment and different severity of leukoaraiosisAlberto Chiti, Paolo Cecchi, Ilaria Pesaresi, et al.
Pageof 2