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Alessandro Simonati

Showing results (11-20 of 76) with videos related to

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International Journal of Molecular Sciences|August 14, 2025
Gut-Brain Interactions in Neuronal Ceroid Lipofuscinoses: A Systematic Review Beyond the Brain in Paediatric DementiasStefania Della Vecchia, Maria Marchese, Alessandro Simonati, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 27, 2013
Clinical, ultrastructural, and molecular studies in a patient with Kufs diseaseFrancesca Moro, Floriana Gismondi, Francesco Pezzini, et al.
Journal of the Peripheral Nervous System : JPNS|April 21, 2011
Déjerine-Sottas syndrome with a silent nucleotide change of myelin protein zero geneFederica Taioli, Ilaria Cabrini, Tiziana Cavallaro, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|May 20, 2023
Enhanced expression of the autophagosomal marker LC3-II in detergent-resistant protein lysates from a CLN3 patient's post-mortem brainFrancesco Pezzini, Michele Fiorini, Stefano Doccini, et al.
Journal of Neurology|September 21, 2002
Dejerine-Sottas neuropathy with multiple nerve roots enlargement and hypomyelination associated with a missense mutation of the transmembrane domain of MPZ/P0Alessandro Simonati, Gian Maria Fabrizi, Federica Taioli, et al.
Orphanet Journal of Rare Diseases|June 16, 2026
Psychiatric manifestations in Neuronal ceroid lipofuscinosesStefania Della Vecchia, Alessandro Simonati, Maria Marchese, et al.
Journal of Neurology|June 11, 2003
Central-peripheral sensory axonopathy in a juvenile case of Alpers-Huttenlocher diseaseAlessandro Simonati, Massimiliano Filosto, Giuliano Tomelleri, et al.
Acta Neuropathologica|May 20, 2004
Hepato-cerebral syndrome: genetic and pathological studies in an infant with a dGK mutationMassimiliano Filosto, Michelangelo Mancuso, Giuliano Tomelleri, et al.
Acta Neuropathologica|May 2, 2003
Features of cell death in brain and liver, the target tissues of progressive neuronal degeneration of childhood with liver disease (Alpers-Huttenlocher disease)Alessandro Simonati, Massimiliano Filosto, Chiara Savio, et al.
Seizure|September 16, 2016
Progressive Myoclonus Epilepsy in Congenital Generalized Lipodystrophy type 2: Report of 3 cases and literature reviewRoberta Opri, Gian Maria Fabrizi, Gaetano Cantalupo, et al.
Pageof 8

Showing results (11-20 of 76) with videos related to

Sort By:
Pageof 8
International Journal of Molecular Sciences|August 14, 2025
Gut-Brain Interactions in Neuronal Ceroid Lipofuscinoses: A Systematic Review Beyond the Brain in Paediatric DementiasStefania Della Vecchia, Maria Marchese, Alessandro Simonati, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 27, 2013
Clinical, ultrastructural, and molecular studies in a patient with Kufs diseaseFrancesca Moro, Floriana Gismondi, Francesco Pezzini, et al.
Journal of the Peripheral Nervous System : JPNS|April 21, 2011
Déjerine-Sottas syndrome with a silent nucleotide change of myelin protein zero geneFederica Taioli, Ilaria Cabrini, Tiziana Cavallaro, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|May 20, 2023
Enhanced expression of the autophagosomal marker LC3-II in detergent-resistant protein lysates from a CLN3 patient's post-mortem brainFrancesco Pezzini, Michele Fiorini, Stefano Doccini, et al.
Journal of Neurology|September 21, 2002
Dejerine-Sottas neuropathy with multiple nerve roots enlargement and hypomyelination associated with a missense mutation of the transmembrane domain of MPZ/P0Alessandro Simonati, Gian Maria Fabrizi, Federica Taioli, et al.
Orphanet Journal of Rare Diseases|June 16, 2026
Psychiatric manifestations in Neuronal ceroid lipofuscinosesStefania Della Vecchia, Alessandro Simonati, Maria Marchese, et al.
Journal of Neurology|June 11, 2003
Central-peripheral sensory axonopathy in a juvenile case of Alpers-Huttenlocher diseaseAlessandro Simonati, Massimiliano Filosto, Giuliano Tomelleri, et al.
Acta Neuropathologica|May 20, 2004
Hepato-cerebral syndrome: genetic and pathological studies in an infant with a dGK mutationMassimiliano Filosto, Michelangelo Mancuso, Giuliano Tomelleri, et al.
Acta Neuropathologica|May 2, 2003
Features of cell death in brain and liver, the target tissues of progressive neuronal degeneration of childhood with liver disease (Alpers-Huttenlocher disease)Alessandro Simonati, Massimiliano Filosto, Chiara Savio, et al.
Seizure|September 16, 2016
Progressive Myoclonus Epilepsy in Congenital Generalized Lipodystrophy type 2: Report of 3 cases and literature reviewRoberta Opri, Gian Maria Fabrizi, Gaetano Cantalupo, et al.
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